This box hooks students into the study of genetics by investigating the inheritance of human traits. Drawn by students' natural curiosity about how they come to look the way they do, they learn the basics of Mendelian genetics. From this introduction, students extract DNA, build DNA models and use them to study replication, transcription and translation. The DNA activities culminate in a CSI investigation in which students must solve a mystery using DNA fingerprinting. The unit then zooms back out from the molecular level to look at natural selection and the evolution of species. A version of the classic bird beak buffet activity is provided as well a wide variety of extensions to delve into evolution in greater detail.
Summary
Genes and DNA are very abstract concepts for students. In order to "hook" them in, I open my genetics and evolution unit with human genetics, specifically looking at the variations in human traits. This allows students' natural curiosity about their identity to draw them into the study of heredity. There are lots of great single gene traits with simple dominance inheritance patterns to explore: earlobe attachment, tongue rolling, cleft chin, etc. There are some polygenic traits that can be explored: hair color, eye color, reach, reaction time, etc. Hair texture (curly, wavy, vs. straight) offers a good example of incomplete dominance. After collecting information from themselves and two others, the population data is collected on several large charts in order to look for and discuss the patterns.
Objectives
Can describe human traits.
Can distinguish between single gene and polygenic traits.
Can use tables to organize data and create histograms to graphically represent data.
Can identify patterns in data and draw conclusions from those patterns.
Vocabulary
Characteristic
Trait
Gene
Polygenic
Histogram
Attachment | Size |
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1traits_survey.doc | 56.5 KB |
traits_handout.doc | 624.5 KB |
traits_handout.pdf | 844.61 KB |
Time
Introduction - 30 min
Collect, organize and analyze data - 50 to 100 min depending on the depth of your analysis
Grouping
Small groups in class and at home for data collection. Whole class for the analysis of the collected data.
Materials
Setting
Classroom.
Teacher Background
If you were asked to describe yourself to a stranger so they could recognize you at the airport, what would you say? What traits make you unique and different from others? The general ways one person can different from another – height, eye color, hair color, build, complexion, etc – are called characteristics. The precise description of an individual – 5’2”, brown eyes, brown hair, fairly thin, etc. – are called the person’s traits.
In this activity, students survey themselves and others that aren’t in the school for a wide array of traits. Some are “yes/no” traits – dimples/no dimples, freckles/no freckles, attached earlobes/unattached earlobes, etc. Others are “multiple choice” traits – blond/red/brown/black hair, blue/green/hazel/brown eyes, etc. Others vary even more widely – reaction time, hand span, reach, etc. In fact, most of these when plotted on a histogram will generate a bell curve.
These differences relate to the number of genes controlling that characteristic. Most simple “yes/no” traits are controlled by a single gene. Most “multiple choice” traits are controlled by a small number (2-4) genes. The widely varying traits are governed by a large number of genes.
In running this activity, it is essential to be sensitive to the different family situations your students may be in. In the past, it has been traditional to survey one’s immediate family for a series of traits and generate a family pedigree. However, with the number of divorced, adopted, single-parent, and same-sex families in our schools today, it becomes much more difficult to negotiate a unit on inheritance without hurting someone’s feelings. Therefore, my approach is to ask students to survey any two people from outside the school. If it is possible to survey your biological parents, great! If not, any two people from outside school is fine.
Student Prerequisites
None
Getting Ready
Day 1 - Introduction
Day 2 - Collect and organize data
Lesson Plan
Day 1 - Introduction
Day 2 – Collect and organize data
Day 3 – Analyze data
- Discuss the difference between the traits measured in centimeters versus the yes/no/multiple choice traits. How many possible outcomes were there for traits measured in centimeters? If the yes/no/multiple choice traits were plotted on a histogram, what would the histogram look like? What is the biological difference between these 2 categories (traits measured in centimeters depend on many genes while yes/no/multiple choice traits depend on a small number of genes)?
- Discuss the evolutionary advantage of different traits. Is there an advantage to having a broad hand span? Is there an advantage to having a small hand span?
- Lead the discussion into a description of basic Mendelian genetics. For each of the yes/no traits, one trait is dominant and the other is recessive (see Making Babies lab for additional information). Eye color and hair color are more complicated because they are determined by multiple genes. Hair texture is more complicated because it is determined by codominance. Discuss how each person has 2 genes for each trait, one from mom and one from dad. The combination of these genes is what determines your traits.
Assessment
Going Further
Sources
The idea for this activity was inspired by Katie Ward, a superwoman science teacher from Aragon High School. Another traits survey activity for the classroom with a slightly different twist can be found through the NASA Explores website.
Any resource list I might compile would be incomplete next to the genetics resource list created by 42Explore.
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
c. Students know an inherited trait can be determined by one or more genes.
d. Students know plant and animal cells contain many thousands of different genes and typically have two copies of every gene. The two copies (or alleles) of the gene may or may not be identical, and one may be dominant in determining the phenotype while the other is recessive.
Summary
This is an extension of the Human Traits survey activity designed to introduce students to genes, genotypes, and simple inheritance patterns. Using information from the Human Traits Survey, students make guesses about their own genotype, create gametes from their genotypes, then make “babies” with a partner. Along the way students discover answers to the questions: What are genes? How are genes (and traits) passed on? How are gametes different than other cells in our body? Why do I look like mom in some ways and dad in other ways and neither of them in still other ways? Why don’t siblings look alike?
Objectives
Can explain the relationship between genotype and phenotype.
Can explain the inheritance of single gene traits using dominant/recessive relationships.
Can take genotype information from 2 parents, model the creation of gametes by independent assortment, and use those gametes to create offspring.
Vocabulary
Trait
Phenotype
Genotype
Gene
Allele
Dominant
Recessive
Incomplete dominance
Homozygous
Heterozygous
Gamete
Zygote
Attachment | Size |
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babies_handout.doc | 60.5 KB |
2making_babies.doc | 61 KB |
Time
50 minutes
Grouping
Individual initially then later in pairs. The teacher should devise a way to break the students into pairs (ramdomly or assign beforehand). Allowing students to pick their own partners is NOT a good idea for this activity. It is not necessary to have mixed gender pairs. In fact, the same gender pairs tended to be more mature about the whole thing.
Materials
Setting
Classroom
Teacher Background
One of the greatest mysteries – how we inherit traits from our parents – was solved in the 1800s by the Austrian monk Gregor Mendel. Although he published his work in 1866, it went almost entirely unrecognized until the 1900s, long after his death.
Mendel worked with pea plants, carefully characterizing their traits and cross-breeding them over many generations. He observed that many traits occur in only two different forms (short or long stems, purple or white flowers, round or wrinkled seeds). When a short plant is crossed with a tall plant, the offspring are all either tall or short, not of middle stem length. This observation countered the “blending theory” that was generally accepted at the time.
Mendels peasHe established many pure-breeding lines – for instance short plants that when cross-bred always had short offspring and tall plants that always had tall offspring. Interestingly, when a pure-bred short plant is crossed with a pure-bred tall plant, the first offspring (f1 generation) are all tall! If these tall f1 plants are cross-bred to one another, the next generation (f2) consistently have a 3:1 ratio of tall to short plants.
With these ratios and careful breeding experiments, Mendel discovered the basic laws of inheritance. He came to several conclusions:
Thus, what happened in Mendel’s tall x short plant experiment was this… The pure breeding tall plant can be represented by TT. The pure breeding short plant can be represented by tt. Each letter (T or t) represents one factor or gene. Since each individual has 2 copies of every factor or gene, each plant has 2 letters to represent its combination of genes (its genotype). The different forms of the gene (alleles) are represented by capital versus lower case letters.
When the tall and short plants were crossed, each parent gave the offspring one of its two genes. The result is that all the offspring inherit the combination Tt. All of these f1 plants are tall. Thus, the tall T allele covers up the short t allele resulting in tall f1 offspring. The tall T allele is therefore said to be dominant over the short t allele and the short t allele is recessive to the tall T allele.
These tall f1 plants with the genotype Tt are then crossed to one another. Since the offspring can be given a tall T allele or a short t allele, there are 4 possible combinations that may occur, each are equally likely: TT, Tt, tT or tt. Only tt would produce a short plant since in all the other cases, the dominant tall T allele is present to cover up any recessive short t alleles that might be present. Thus, there is a 3:1 ratio of tall to short plants in this f2 generation.
This can be graphically shown in what is known as a Punnett square which resembles a multiplication table as shown at left.
This inheritance pattern is simplest of all possibilities. It gets a whole lot more complex when you consider incomplete dominance (where the heterozygotes that have two different alleles like Tt have an intermediate phenotype), X linkage (what happens with genes on the sex chromosomes), polygenetic traits (traits determined by more than one gene), linked genes (genes that often go together because they are located close to one another on the same chromosome), and more.
In this activity, we examine some human facial traits that are assumed to be single gene traits. The actual genetics is MUCH more complex. However a brief run-down is provided here (for photos of the traits listed below, see attachment at the bottom of the Human Traits activity):
There are a few traits to be cautious about using with students because people have a difficult time accurately recording traits. For instance, nearsightedness is a single gene trait with normal vision dominant to nearsightedness. However, kids often aren’t diagnosed with nearsightedness until late in adolescence. This leads to awkward questions such as, “Both my parents are nearsighted but I’m not. Does that mean I’m adopted?” Often teachers use round versus square shaped faces in which round faces are dominant to square faces. Both me and my students have difficulty categorizing faces as round or square, leading to much confusion. Other traits that are often difficult to categorize include: lip shape, eye spacing, eyelash length, eye slant, nose shape, and eyebrow thickness. Finally, be sure to warn students that in categorizing freckles, DO NOT COUNT sun freckles. Freckles means a very large number of freckles all over the nose and cheeks, whether you’ve been in the sun or not.
Student Prerequisites
Completion of the Human Traits activity.
Getting Ready
Lesson Plan
Assessment
- Who was Gregor Mendel?
- In one experiment, Mendel crossed a tall pea plant with a short pea plant. What kind of eggs and pollen are produced? What is the genotype of the baby plant? What is the phenotype of the baby plant?
- Next, he took these tall hybrids and bred them together. How many of these grandchild plants were tall? How many of these grandchild plants were short? Explain how it is possible for 2 tall pea plants to have a short baby.
- Why were Gregor Mendel’s experiments important?
- A brown eyed mom and a blue eyed dad have a blue eyed baby. What is the genotype of the baby? What is the genotype of the dad? What are two possible genotypes for the mom? Which genotype must she be to have a blue eyed baby? Explain why she must be this genotype.
Going Further
Sources
This lesson was adapted from a lesson by Katie Ward of Aragon High School in San Mateo. After trying Katie’s version with my students, I found several other similar activities on the web. For instance, see the Making Babies lab written by Kevin Hartzog of Thurgood Marshall Academic High School. Kevin Hartzog's website Stars and Seas is extraordinary! With lots of other great lessons and ideas. Also recommended is this Making Babies lab from Friends Academy .
For information about Mendelian genetics, see:
For more information on the inheritance of human traits such as eye color, hair color, and tongue rolling, see:
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
b. Students know sexual reproduction produces offspring that inherit half their genes from each parent.
c. Students know an inherited trait can be determined by one or more genes.
d. Students know plant and animal cells contain many thousands of different genes and typically have two copies of every gene. The two copies (or alleles) of the gene may or may not be identical, and one may be dominant in determining the phenotype while the other is recessive.
Grades 9-12
Genetics
2. Mutation and sexual reproduction lead to genetic variation in a population. As a basis for understanding this concept:
a. Students know meiosis is an early step in sexual reproduction in which the pairs of chromosomes separate and segregate randomly during cell division to produce gametes containing one chromosome of each type.
b. Students know only certain cells in a multicellular organism undergo meiosis.
c. Students know how random chromosome segregation explains the probability that a particular allele will be in a gamete.
d. Students know new combinations of alleles may be generated in a zygote through the fusion of male and female gametes (fertilization).
e. Students know why approximately half of an individual's DNA sequence comes from each parent.
f. Students know the role of chromosomes in determining an individual's sex.
g. Students know how to predict possible combinations of alleles in a zygote from the genetic makeup of the parents.
3. A multicellular organism develops from a single zygote, and its phenotype depends on its genotype, which is established at fertilization. As a basis for understanding this concept:
a. Students know how to predict the probable outcome of phenotypes in a genetic cross from the genotypes of the parents and mode of inheritance (autosomal or X-linked, dominant or recessive).
b. Students know the genetic basis for Mendel's laws of segregation and independent assortment.
c. * Students know how to predict the probable mode of inheritance from a pedigree diagram showing phenotypes.
Strawberry DNA: The cloudy substance in the upper layer is strawberry DNA.Summary
What is DNA? What does it look like? In this activity, students extract DNA from strawberries using diluted dish soap and alcohol. Suddenly this mysterious secret of life can be seen materializing out of strawberry juice right in front of students’ eyes. The long tangled DNA strands that ultimately form may be collected using a bamboo skewer or glass stirring rod. The DNA may even be saved in a necklace made from an eppendrof tube, alcohol and string.
Objectives
Can extract DNA.
Can recognize that DNA is found in all cells.
Can explain the steps needed to isolate DNA from a cell.
Can begin to describe the structure of DNA – that it is a long, invisibly thin polymer.
Vocabulary
DNA
Nucleus
Cell
Membrane
Attachment | Size |
---|---|
3dna_extraction.doc | 52.5 KB |
Time
40 minutes
Grouping
individual
Materials
Each student needs:
Extraction buffer recipe:
Optional for making necklaces:
For the whole class to share:
Setting
Classroom
Teacher Background
This activity should be part of the standard repertoire of any teacher who teaches genetics. It is essential for students to prove to themselves that DNA exists and that it can be extracted from any cell. Strawberries are used in this activity because they are octaploid, meaning they have 8 copies of every gene rather than the usual 2; thus providing prodigious quantities of DNA to extract. Naturally, strawberries are also relatively inexpensive and readily available. Other sources of DNA to experiment with include kiwis, bananas, and calf thymus.
The DNA molecule is an invisibly thin, very long strand. The DNA found in each human cell is almost 2 meters long. If all the DNA in a human adult (that’s 100 trillion cells) were laid end to end, the DNA would stretch 113 billion miles. That would take you to the sun and back 610 times. Even though DNA is invisible to the naked eye, no microscopes are needed! The reason is that you release so many DNA strands that they tangle together into a thick cable, visible without magnification. For example, it would be the same as if you took a thin piece of thread and held it up on the far end of the hallway. You probably wouldn’t be able to see the thread from that distance. However, if you took the thread and tangled it up with a hundred thousand other threads, you would be able to see the tangled clump from far away because there is so much of it.
The process itself is fairly straightforward. First the cell walls are broken open by smashing the strawberries in a ziplock bag. Next, detergent is used to dissolve the cell and nuclear membranes. The membranes are made of lipids (fat) and the detergent will cut through the membrane just like it cuts through grease on a dirty plate when washing dishes. Some salt is present in the detergent solution in order to match the osmolarity of the cells.
Now you have a big mixture of smashed cell walls, dissolved membranes, loose DNA and random other cell parts. This mixture is filtered through paper towels. Finally, you take advantage of the fact that DNA is soluble in water but not in alcohol. In fact, alcohol makes DNA clump together. Thus a layer of alcohol laid on top of the filtrate. Any DNA that contacts the alcohol will clump together, pulling the rest of the DNA strand along behind it. Soon you should see gossamer white strands of DNA bubbling their way up from the red strawberry extract.
The DNA may be collected by twirling a bamboo skewer or glass stirring rod in the solution. The DNA will spool itself around the skewer and can be pulled out of the solution. To keep some DNA, students may fill an eppendorf tube with alcohol and place their spooled DNA into the container. Lay the string on the hinge holding the cap to the tube and close the lid. The string forms a necklace with the eppendorf and enclosed DNA as a pendant. Top off the alcohol in the pendant and you can keep the DNA indefinitely.
Student Prerequisites
Some cell biology experience (enough to know that DNA is located in the nucleus of a cell and that membranes are made of lipids) is useful. If students are not aware of these fact, expect to spend at least 10 minutes longer teaching these ideas before starting the extraction.
Getting Ready
Lesson Plan
Assessment
- Why is it necessary to mash the strawberries?
- What is the purpose of the detergent?
- What is the purpose of the salt?
- Name a liquid that DNA is not soluble in.
- Is the DNA that you extracted pure? What else might be attached to the DNA?
- Why might some people get more DNA than others?
- Can you see a single strand of DNA without a microscope? Explain how you were able to see the DNA in this experiment without magnification.
Going Further
Sources
There are numerous write ups for this experiment available on the internet and elsewhere. I first experienced this lesson through UCSF’s Science and Health Education Partnership. I then tried it with Carolina Biological .
The estimates of the length of DNA in a human cell and the number of cells in the human body were taken from Wikipedia (from the Genome and Cell Biology articles).
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
e. Students know DNA (deoxyribonucleic acid) is the genetic material of living organisms and is located in the chromosomes of each cell.
Grades 9-12
Genetics
5. The genetic composition of cells can be altered by incorporation of exogenous DNA into the cells. As a basis for understanding this concept:
a. Students know the general structures and functions of DNA, RNA, and protein.
Summary
DNA structure: click on the image to see it rotateIn this activity, students “discover” the structure of DNA by playing with puzzle pieces representing the component pieces of the DNA molecule: the sugar deoxyribose, phosphate groups, and the 4 nucleic acids (adenine, thymine, cytosine and guanine). The process the students go through in putting the puzzle together resembles the way James Watson and Francis Crick deduced the molecular structure of DNA by manipulating molecular models of the component pieces (and a heavy reliance on the prior experimental work of Rosalind Franklin, Maurice Wilkins, and Erwin Chargaff). The model created by the students makes a lovely classroom decoration and reference for discussing DNA replication, transcription and translation.
Objectives
Can model and describe the general structure of DNA.
Can apply base pairing rules to assemble a DNA molecule.
Can infer that the sequence of the nucleic acids in DNA is the key to how DNA provides instructions to the cell.
Can relate this DNA puzzle activity to Watson and Crick’s original discovery of the structure of DNA.
Assembling the DNA puzzleVocabulary
DNA
Deoxyribose
Phosphate
Nucleic acid
Adenine
Thymine
Cytosine
Guanine
Base pairs
Nucleotide
Attachment | Size |
---|---|
4dna_models.doc | 59.5 KB |
dna_pieces.pdf | 1.09 MB |
Time
30 minutes to cut DNA model pieces (It is possible to assign each student a sheet of puzzle pieces to cut out as homework the night before.)
20 minutes to assemble puzzle
10 minutes to tape puzzle together
10-20 minutes to discuss DNA structure and the discovery of the DNA structure
Grouping
Individual students gradually linking their puzzles together to create a long strand.
Materials
Setting
classroom
Teacher Background
Although DNA was isolated in the 1800s, it was not until the 1900s that scientists believed DNA might store genetic information. By 1929, the 3 major components – the sugar deoxyribose, a phosphate group, and a nucleic acid – had been identified. Furthermore, it was known that the phosphate groups linked the molecule together in a long polymer, however it was assumed that the chains were short and that the bases repeated in the same fixed order.
Towards the late 1940s, more and more came to be known. Erwin Chargaff noticed that in any species he studied, the quantity of adenine was always the same as the quantity of thymine while the amount of guanine was the same as the amount of cytosine. This came to be known as “Chargaff’s ratios”. But what did these rations mean? At around the same time, X-ray diffraction data indicated that DNA was coiled in a helical structure. But how many chains were part of the helix? Did the nucleic acids point in toward the center our face out?
Rosalind Franklin: Rosalind FranklinJames Watson and Francis Crick deduced the structure of DNA in 1953. There were several events that helped them put together the puzzle. First and foremost, the meticulous X-ray diffraction work of Rosalind Franklin and Maurice Wilkins clearly illustrated that the DNA molecule consisted of 2 strands, a double helix, with the nucleic acids on the inside of the molecule. Moreover, the distance between the strands and the pitch of the helix could be precisely measured. With this information, Watson and Crick were able to build a model of the sugar-phosphate backbone of DNA.
The final step of the solution required the use of cardboard models of the 4 nucleic acids. Watson and Crick cut out precise shapes for each nucleic acid. On the hunch that Chargaff’s rule implied a pairing between adenine-thymine and cytosine-guanine, they played with their puzzle pieces to see how they might fit together. They realized that in just the right orientation, adenine-thymine and cytosine-guanine pairs were almost identical in shape, thus providing equally spaced rungs between the 2 backbones of the ladder.
Watson and Crick DNA model: Physical model built by James Watson and Francis Crick to deduce the structure of DNA. Currently on display in the National Science Museum of London.
Watson and Crick published their work in 1953 alongside an article by Franklin and Wilkins showing the X-ray diffraction data. In 1962, Watson, Crick and Wilkins were awarded the Nobel Prize for discovering the structure of DNA. By that time, Franklin had died of ovarian cancer. Since Nobel prizes are not awarded posthumously, Franklin could not share in the honor.
Thus the structure of DNA can be said to be composed of two sugar-phosphate backbones, oriented in opposite directions to one another (notice how the sugars on one side are upside-down compared to the sugars on the other strand). The sugars are then attached to a nucleic acid. The nucleic acids are paired such that adenine is always matched to thymine with 2 hydrogen bonds while guanine is always matched to cytosine with 3 hydrogen bonds. A matching pair of nucleic acids is called a base pair. The assembly of one phosphate, sugar and nucleic acid is called a nucleotide.
Student Prerequisites
None
Getting Ready
Lesson Plan
Assessment
Going Further
Sources
This activity was adapted from a DNA model designed by Lori Lambertson of the Exploratorium Teacher Institute.
For additional background materials, see:
Standards
Grade 7
Cell Biology
1. All living organisms are composed of cells, from just one to many trillions, whose details usually are visible only through a microscope. As a basis for understanding this concept:
c. Students know the nucleus is the repository for genetic information in plant and animal cells.
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
e. Students know DNA (deoxyribonucleic acid) is the genetic material of living organisms and is located in the chromosomes of each cell.
Grade 8
Chemistry of Living Systems (Life Sciences)
6. Principles of chemistry underlie the functioning of biological systems. As a basis for understanding this concept:
c. Students know that living organisms have many different kinds of molecules, including small ones, such as water and salt, and very large ones, such as carbohydrates, fats, proteins, and DNA.
Grades 9-12
Genetics
5. The genetic composition of cells can be altered by incorporation of exogenous DNA into the cells. As a basis for understanding this concept:
a. Students know the general structures and functions of DNA, RNA, and protein.
b. Students know how to apply base-pairing rules to explain precise copying of DNA during semiconservative replication and transcription of information from DNA into mRNA.
Summary
Kids love secret codes and secret messages. In this activity, kids first discover how codes work by reading and writing secret messages written in Morse code. Next, they make up their own secret codes and trade messages written in their self-created code. Finally, students learn how DNA codes for a “secret” protein message in a two step coding system – the genetic code. Since each of the 20 amino acids has a one letter abbreviation, student can discover the secret protein “messages” encoded in a DNA strand. Several secret DNA messages are provided for students to decode under the assessments section. For homework, students can be challenged to write a secret message to a friend using the genetic code.
Objectives
Can explain how DNA codes for a sequence of amino acids.
Can begin to explain some of the differences between DNA and RNA.
Can begin to describe the process of transcription and translation.
Vocabulary
DNA
Messenger RNA
Ribosome
Amino acids
Protein
Codon
Morse code
Genetic code
Transcription
Translation
Attachment | Size |
---|---|
5secret_codes.doc | 48.5 KB |
codes_handout.doc | 43 KB |
Time
45-55 minutes
Grouping
Individual
Materials
Setting
classroom
Teacher Background
The genetic code is a set of rules that guide how the sequence of DNA nucleotides is read by a cells machinery and turned into a sequence of amino acids that make up a protein. Incredibly, nearly all living things use the same genetic code!
To understand how DNA provides the instructions for making proteins, one first needs to understand a little about what a protein is. A protein, like DNA, is a polymer (a long molecule that is a chain of smaller repeating subunits). The subunits in proteins are called amino acids. There are 20 different amino acids that can be linked together in an infinite array of sequences of different lengths. These chains of amino acids form the proteins that do all the work in our bodies – building cells, generating energy, transporting materials, and more. For this activity, it is important to note that each amino acids has been assigned a single letter abbreviation which allows students to create protein “words” and “messages” with different sequences of amino acids.
The DNA in a cell can be divided into functional units called genes. Each gene provides the instructions for making one protein. Thus, one can think of a gene as a long paragraph describing how to make a protein. The “letters” in the paragraph are the nucleotides (the A’s, T’s, C’s and G’s). The “words” within the gene are made of a sequence of 3 nucleotides, each of which specifies one amino acid in the protein. For instance, the DNA sequence, TAC, specifies the amino acid, methionine. Each nucleotide triplet that codes for an amino acid is called a “codon”.
The process of protein synthesis (reading the DNA codons and translating it into a sequence of amino acids) is a gorgeous, choreographed process involving many steps. For more detail on protein synthesis and the molecules involved, see the background section in the Protein Factory activity.
For the purposes of this activity, one needs to know that the DNA is trapped in the nucleus (at least in plant and animal cells) while the protein making apparatus, the ribosome, is located outside the nucleus in the cytosol. Therefore, a messenger molecule, messenger RNA, is used to copy the DNA message and bring it to the ribosome. RNA is closely related to DNA. They both are polymers of nucleotides with a sugar-phosphate backbone. The differences are that RNA is single stranded, while DNA is double stranded. Furthermore, RNA uses the nucleic acid, uracil, instead of thymine. Finally, instead of the sugar deoxyribose in the backbone, RNA uses the sugar ribose.
Protein synthesis can be summarized in 2 steps:
In this activity, students become familiar with the idea of a coded message by practicing with Morse code. Morse code uses a sequence of dashes and dots to represent the letters of the alphabet, numbers and punctuation. It was developed in the 1830’s for early telegraph and radio communications. Once they get the idea, they have an opportunity to make up their own secret codes, with a different symbol (letter, number, picture) to represent each letter of the alphabet. They write a message to a classmate in their secret code. The keys and coded messages are traded and students can decode each others’ messages.
Then, they are told about how a strand of DNA can be turned into RNA and then into a string of amino acids. Using the one letter abbreviations of the amino acids, secret messages may be written and decoded using the genetic code. The idea of a genetic code can be compared to Morse code and their self-created codes. I have found that this activity makes the big picture of protein synthesis much easier for students to understand than jumping straight into the details of the molecules involved and how they all interact.
Student Prerequisites
A solid understanding of DNA structure is essential. A basic understanding of what a protein is and its structure is helpful but not required.
Getting Ready
Lesson Plan
Assessment
Going Further
Standards
Grade 8
Chemistry of Living Systems (Life Sciences)
6. Principles of chemistry underlie the functioning of biological systems. As a basis for understanding this concept:
c. Students know that living organisms have many different kinds of molecules, including small ones, such as water and salt, and very large ones, such as carbohydrates, fats, proteins, and DNA.
Grade 9-12
Genetics
4. Genes are a set of instructions encoded in the DNA sequence of each organism that specify the sequence of amino acids in proteins characteristic of that organism. As a basis for understanding this concept:
a. Students know the general pathway by which ribosomes synthesize proteins, using tRNAs to translate genetic information in mRNA.
b. Students know how to apply the genetic coding rules to predict the sequence of amino acids from a sequence of codons in RNA.
e. Students know proteins can differ from one another in the number and sequence of amino acids.
Summary
Using a DNA model like the one created in the DNA Models lesson, students take on the role of various parts of the cell in order to model the process of protein synthesis. Each student receives a card describing, step by step, what s/he should be doing. In a class of 30:
Objectives
Can explain how DNA codes for a sequence of amino acids.
Can explain the differences between DNA and RNA.
Can describe the process of transcription and translation.
Vocabulary
DNA
Nucleotide
RNA polymerase
Promotor
Uracil
Messenger RNA
Ribosome
Transfer RNA
Amino acids
Protein
Genetic code
Codon
Anticodon
Transcription
Translation
Attachment | Size |
---|---|
6protein_factory.doc | 59 KB |
factory_instructions.doc | 37 KB |
protein_pieces.pdf | 638.23 KB |
Time
45-55 minutes
Grouping
Whole class.
Materials
Setting
classroom
Teacher Background
The process of turning DNA into protein is called the “central dogma of molecular biology” because it is the foundation of all modern genetics, biotech and pharmacology. There are 6 major players in the process.
Transcription and translation: Illustration from Radboud University NijmegenThere are 2 major steps in the protein synthesis process. The first is the synthesis of messenger RNA in a process known as transcription. This process is similar to DNA replication, except that only a tiny portion of one strand is copied and it is copied into a single-stranded RNA molecule, not a double stranded DNA molecule.
To start transcription, RNA polymerase binds to a specific DNA sequence known as a promotor. Promotors sequences are very diverse, however, generally are found in the stretch of DNA in front of the gene and contain a place for RNA polymerase to bind as well as a transcriptional start sequence that indicates where transcription should begin. They range in length from less than a hundred base pairs to several thousand base pairs. Many promotor sequences contain the sequence TATAAA, known as a TATA box by biologists. This TATAAA sequence is used in this activity to indicate where the RNA polymerase should bind and begin transcription.
Once, the RNA polymerase binds to the promotor, it follows along the DNA, unzipping the base pairs, reading one of the two DNA strands, matching an RNA nucleotide to each DNA nucleotide, and assembling a messenger RNA molecule. The RNA polymerase continues moving along the DNA until it reaches a specific terminator sequence, at which point it releases the messenger RNA and disassembles. Messenger RNA molecules may extend over 2 million bases in length. At this point, the messenger RNA travels out of the nucleus to the ribosome where proteins are actually made.
This second step of the protein synthesis process is known as translation. First, a ribosome assembles around the messenger RNA molecule. Translation always begins at the messenger RNA sequence AUG. The messenger RNA then feeds its way through the ribosome like a tape. As it proceeds, each codon on the messenger RNA is matched to a transfer RNA. The ribosome forms bonds between the amino acids carried by the transfer RNAs and the empty transfer RNA molecules detach and float away. Gradually, the amino acid chain grows longer and longer until a stop sequence (UAG, UAA, or UGA) is reached. At that point, the protein is released.
From here, the protein may go through many stages of further processing. Depending on the sequence of amino acids, some parts of the protein like water and some curl away from it. Thus, the protein will fold itself up to protect the water-hating parts of the protein from the surrounding cytosol. In addition, proteins may be cut, spliced, joined together, packaged and reshaped into a final functional protein.
Student Prerequisites
Some basic introduction to the protein synthesis process (see Secret Codes lesson).
Getting Ready
Lesson Plan
- RNA polymerase finds the TATAAA promotor sequence on the DNA molecule.
- RNA polymerase unzips the DNA nucleotide after the promotor and finds a matching RNA nucleotide.
- RNA polymerase unzips the next DNA nucleotide and finds a matching RNA nucleotide.
- RNA polymerase joins the RNA nucleotides together.
- RNA polymerase continues unzipping, finding nucleotides, and joining them together until the end of the DNA molecule.
- DNA zips itself back up again.
- The newly assembled messenger RNA floats out of the nucleus to the ribosome.
- The ribosome finds the AUG start sequence on the messenger RNA.
- The ribosome finds a matching transfer RNA and lines it up alongside the messenger RNA strand.
- The ribosome finds a matching transfer RNA to the next 3 nucleotides.
- The ribosome removes the amino acid from the first transfer RNA and attaches it to the amino acid that just arrived.
- The ribosome continues finding transfer RNA molecules and joining amino acids until it reaches a stop codon (UAG, UAA, or UGA).
- The empty transfer RNA molecules leave the ribosome.
Assessment
Sources
This activity was put together from the bright ideas of several great teachers: Lori Lambertson of the Exploratorium Teacher Institute and Jim Youngblom of CSU Stanislaus.
Standards
Grade 8
Chemistry of Living Systems (Life Sciences)
6. Principles of chemistry underlie the functioning of biological systems. As a basis for understanding this concept:
c. Students know that living organisms have many different kinds of molecules, including small ones, such as water and salt, and very large ones, such as carbohydrates, fats, proteins, and DNA.
Grade 9-12
Genetics
4. Genes are a set of instructions encoded in the DNA sequence of each organism that specify the sequence of amino acids in proteins characteristic of that organism. As a basis for understanding this concept:
a. Students know the general pathway by which ribosomes synthesize proteins, using tRNAs to translate genetic information in mRNA.
b. Students know how to apply the genetic coding rules to predict the sequence of amino acids from a sequence of codons in RNA.
e. Students know proteins can differ from one another in the number and sequence of amino acids.
DNA adding tapeSummary
In this CSI activity, students solve a mystery using “DNA” taken from the scene of the crime. This write up describes how to collect a “DNA sample” (student invented DNA sequence on adding machine tape) from the culprit and from each person in the class, then run the DNA on a “gel” that covers the floor of the classroom, a hallway, or gymnasium. Naturally, the CSI aspect can become as elaborate as you wish by including additional “clues” such as fingerprints, a ransom note written in a specific type of ink, cloth fibers, eyewitness accounts and more. Since both DNA fingerprinting and paper chromatography (see Sources for lesson plans) rely on the same principles – separating molecules by size – a crime scene in which there is both a note written in a specific type of water-based ink as well as a DNA sample that may compared to the students’ DNA draws some interesting parallels conceptually between these two CSI techniques.
Objectives
Can explain what restriction enzymes do.
Can explain how gel electrophoresis works.
Can describe DNA fingerprinting methods.
Can discuss some of the considerations in evaluating DNA evidence in a crime.
Vocabulary
DNA replication
DNA polymerase
DNA fingerprinting
Restriction enzyme
Restriction fragment length polymorphisms
Short tandem repeats
Polymerase chain reaction
Gel electrophoresis
Attachment | Size |
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7dna_fingerprint.doc | 68 KB |
Time
Day 1+: Investigating the crime scene (may take up to a week depending on the complexity of the evidence)
Day 2: Creating DNA samples and replicating DNA
Day 3: Running the “gel” and analyzing DNA fingerprint results
Grouping
Crime scene may be studied in teams or as a whole class. DNA samples are created and replicated individually. The gel is run and analyzed as a whole class.
Materials
Setting
Classroom and possibly a hallway or gym to “run” your “gel”.
Teacher Background
The crux of this activity is the creation of a DNA sequence on a strip of adding tape, replication of the DNA, then using these DNA sequences to perform DNA fingerprinting.
DNA replicationThe base pairing rules help explain the process of DNA replication – how a cell makes an exact copy each strand of DNA just before it divides. First, an enzyme called helicase unzips the DNA down the middle of the ladder, in between the base pairs. Next, an enzyme called DNA polymerase reads one half of the strand, identifies a matching nucleotide, and builds a new partner strand. The process is complicated by the fact that DNA polymerase can only work in one direction along the sugar-phosphate backbone (remember, that the 2 backbones are oriented in opposite directions to one another). Thus, while DNA polymerase can easily run continuously along one strand, known as the “leading” strand, the other “lagging strand” must be assembled in a piecemeal fashion, one section at a time.
DNA fingerprinting is a technique used to distinguish between individuals of the same species using only samples of their DNA. Its invention by Sir Alec Jeffreys at the University of Leicester was announced in 1985.
DNA fingerprinting is used in forensic science, to match suspects to samples of blood, hair, saliva or semen. It has also led to several exonerations of formerly convicted suspects. It is also used in such applications as studying populations of wild animals, paternity testing, identifying dead bodies, and establishing the province or composition of foods. It has also been used to generate hypotheses on the pattern of the human diaspora in prehistoric times.
Two humans will have the vast majority of their DNA sequence in common. The traditional method of DNA fingerprinting uses restriction enzymes that cuts DNA at a specific sequence. Restriction enzymes work by recognizing a specific DNA sequence and cutting the DNA within this sequence. For instance, the restriction enzyme known as Sma1 looks for the sequence CCCGGG and cuts the DNA between the middle C and G. Other restriction enzymes make a staggered cut with some overhang on each end. For instance, the restriction enzyme EcoR1 looks for the sequence GAATTC and makes a staggered cut leaving what is known as a sticky end.
If designed correctly, a restriction enzyme can target a part of the genome that his highly variable from person to person such that some individuals’ DNA will be cut while others won’t, resulting in variable length DNA pieces. These differences are known as restriction fragment length polymorphisms. This technique is also often used to determine an individual’s genotype for a given gene – for instance, to test for the presence or absence of a mutation that confers a certain genetic disorder.
These DNA pieces may then be separated using gel electrophoresis. This method places the DNA sample in a well on one end of a sheet of agarose gel, similar to a thin layer of jello. An electric field is then applied to the gel. Since DNA is negatively charged, it is attracted to the positive end of the field and begins moving through the gel. The larger, longer fragments cannot travel as far through the gel matrix and get trapped near where the sample is loaded. The smaller, shorter fragments can wiggle their way through the matrix more easily and thus travel further. This results in a unique pattern of bands for each individual, depending on the DNA sequence.
Another common method of DNA fingerprinting exploits highly variable repeating sequences called short tandem repeats (STRs). Different people have different numbers of repeat units. For instance, the CSF gene contains the sequence AGAT repeated anywhere between 6 to 16 times. Two unrelated humans will be likely to have different numbers of this AGAT sequence.
While the variable number of repeats displayed at any single STR region will be shared by around 5 – 20% of individuals, if you look at several STR regions simultaneously, this method becomes incredibly powerful. The more STR regions that are tested in an individual the more discriminating the test becomes. In the U.S.A., there are 13 loci (DNA locations) that are currently used for discrimination. This has resulted in the ability to generate match probabilities of 1 in a quintillion (1 with 18 zeros after it) or more. Therefore, it is possible to establish a match that is extremely unlikely to have arisen by coincidence, except in the case of identical twins, who will have identical genetic profiles.
The process begins by extracting DNA from the cells in a sample of blood, saliva, semen, or other appropriate fluid or tissue. Next, each STR region is amplified using polymerase chain reaction (PCR) so that the initially tiny DNA sample is copied many times, creating a sufficiently large pool of DNA for analysis. Finally, the DNA fragments are then separated and detected using gel electrophoresis. Again, the shorter the sequence of repeats, the further the DNA fragment will travel through the gel.
Student Prerequisites
A solid understanding of DNA structure and base pairing rules.
Getting Ready
Lesson Plan
Day 1+ - Investigating the crime scene
If you set up a crime scene, make lots of observations of the crime scene. Start with all the kids outside the crime scene area, drawing pictures and writing down the things they notice. Finally, allow one student at a time enter the crime scene area wearing gloves to collect evidence. Evidence should be kept in plastic bags. Analyze any non-DNA evidence first. Dust for fingerprints. Collect hair and fiber samples. Perform paper chromatography on the ransom note and compare it against the pens in the possession of the various suspects. (See Sources section below for resources and lesson plans describing how to conduct these tests.)
Day 2 – Creating the DNA sequences and replicating DNA
Day 3 – Running the “gel” and analyzing DNA fingerprint results
Assessment
Going Further
Sources
If you are interested in creating a full-fledged CSI experience, an indispensable resource for teachers is the book, Mystery Festival, published by the Lawrence Hall of Science.
Other forensics science resources include:
Finally, for a great real world mystery to solve using DNA analysis among other techniques, go to the “Recovering the Romanovs” from DNA interactive by Cold Spring Harbor. It is quite simply, extraordinary.
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
e. Students know DNA (deoxyribonucleic acid) is the genetic material of living organisms and is located in the chromosomes of each cell.
Grades 9-12
Genetics
4. Genes are a set of instructions encoded in the DNA sequence of each organism that specify the sequence of amino acids in proteins characteristic of that organism. As a basis for understanding this concept:
c. Students know how mutations in the DNA sequence of a gene may or may not affect the expression of the gene or the sequence of amino acids in an encoded protein.
5. The genetic composition of cells can be altered by incorporation of exogenous DNA into the cells. As a basis for understanding this concept:
a. Students know the general structures and functions of DNA, RNA, and protein.
b. Students know how to apply base-pairing rules to explain precise copying of DNA during semiconservative replication and transcription of information from DNA into mRNA.
d. * Students know how basic DNA technology (restriction digestion by endonucleases, gel electrophoresis, ligation, and transformation) is used to construct recombinant DNA molecules.
Summary
Inspired by observations of finches on the Galapagos Islands, Charles Darwin came up with an idea that is perhaps the most influential idea in all of science - natural selection. In this classic activity, students learn about natural selection by becoming birds foraging for food on an island (a large area of the schoolyard or classroom). The prey (beans) vary in their coloration such that some blend into the environment better than others. The birds vary in the type of beak they have (plastic forks, spoons and knives). Each season, any prey that survives has a baby bean the same color as the parent. In addition, the most successful birds has a baby with the same beak trait while the least successful birds die (and are reincarnated as the babies of the successful birds). Over several generations, the bird and bean populations shift depending on the environment. Well camouflaged beans survive and reproduce. Birds with beaks that can easily capture beans survive and reproduce. In this way, students model natural selection in 2 species and get a very good idea of how natural selection works.
Objectives
Can explain what natural selection is and the conditions necessary for it to occur.
Can discuss changes in a population in the context of natural selection.
Can use terms such as natural selection, evolution, and adaptation scientifically.
Can organize data in a table and graph.
Can graph changes in a population over time.
Vocabulary
Trait
Population
Natural selection
Adaptation
Fitness
Evolution
Charles Darwin
Attachment | Size |
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8bird_beak.doc | 69 KB |
bird_beak_student.doc | 60 KB |
bird_beak_data.doc | 67.5 KB |
Time
15-20 minutes introduction
45-50 minutes activity (The lesson plan is written so that the activity is introduced on one day and actually done the following day. It is also possible to introduce the activity and go through one or two years on the first day and complete the activity on the following day.)
15-20 minutes organize and summarize data
30+ minutes discussion
Grouping
Each student is a bird foraging in the same feeding ground. At the end of each year, students gather in a group of similar-beaked birds to enter their foraging results on a clipboard. The introduction and final discussion occurs as a whole class in a classroom.
** If working as a whole class in a single feeding ground is too chaotic for your students, then this activity may be done in smaller groups of 3 or 6. Each group will get their own 1 meter square plot of ground or even a cafeteria tray on a table in the classroom to forage in. Each group starts with 1 or 2 representatives of each of the 3 beak types in the group and 100 beans of each color in the feeding ground. After each season, they should summarize their data and add new beans to their feeding ground. The bird that eats the most will reproduce and the bird that eats the least will die and get reincarnated.**
Materials
Setting
The activity takes place in an 80 square foot (9x9 foot square) feeding ground located in the classroom, on a concrete school yard or in a grassy field. The introduction and post-activity discussion takes place in the classroom.
Teacher Background
Perhaps the most important idea in all of biology, or perhaps all of science, is the idea of evolution through natural selection. This idea by Charles Darwin provides the foundation of all of current scientific thinking in life science.
What is evolution? Quite simply, evolution is descent with modification. This includes both the idea that the frequency of a gene will change in a population over time as environmental conditions change and also the idea that new species descend from common ancestors over many generations. Ultimately, evolution can explain the vast diversity of life on this planet and the idea that all life on Earth shares a common ancestor.
Although there are many mechanisms for organisms to change over time, the most important of these is natural selection. It works in this way:
There are many other mechanisms for evolutionary change besides natural selection:
A final important term that is often misused by students is adaptation. An adaptation is a trait that is very well suited to a given environment that has, through natural selection, increased in the population over many generations. Students often talk and think about adaptation as if an organism can try to adapt or is able to get what it needs. In neither case are they correct. An organism can’t get the genes it needs to survive by “trying”; it either has the genes or not. Similarly, natural selection doesn’t have a goal in mind and cannot give a creature what it “needs”; either the genes are there in the population or not.
In this activity, students come to understand natural selection, evolution and adaptation through modeling changes in 2 populations – a population of birds with different beak traits and a population of beans with different color traits.
Student Prerequisites
None required although an understanding of variation in traits is helpful (see Human Traits activity or Snail Variations project).
Getting Ready
Lesson Plan
Day 1 - Introduction
Day 2 – Bird Beak Buffet
Day 3 – Organize, graph and discuss data
Assessment
Going Further
Sources
The Bird Beak Buffet activity is a classic in the teaching of natural selection and evolution. There are hundreds of write ups out there with all sorts of different variations. I first learned about the activity from Kimberly Tanner, currently faculty at San Francisco State University. I found a box of materials to borrow from Chris Giorni of Tree Frog Treks. Then I participated in a workshop with Karen Kalamuck of the Exploratorium Teachers’ Institute.
There are many variations of this activity on the web from many different organizations:
For background resources on better understanding evolution, nothing beats the Understanding Evolution site from the UC Museum of Paleontology. There you can find everything from evolution 101 to scientific articles to student misconceptions to lesson plans. It’s a one-stop resource for all a teachers’ needs.
Finally, if your school district, administrators or parents opposes the teaching of evolution, see the National Center for Science Education for articles and resources that can help you justify what you are doing in your classroom.
Standards
Grade 7
3. Biological evolution accounts for the diversity of species developed through gradual processes over many generations. As a basis for understanding this concept:
a. Students know both genetic variation and environmental factors are causes of evolution and diversity of organisms.
b. Students know the reasoning used by Charles Darwin in reaching his conclusion that natural selection is the mechanism of evolution.
e. Students know that extinction of a species occurs when the environment changes and the adaptive characteristics of a species are insufficient for its survival.
Grade 9-12
7. The frequency of an allele in a gene pool of a population depends on many factors and may be stable or unstable over time. As a basis for understanding this concept:
a. Students know why natural selection acts on the phenotype rather than the genotype of an organism.
d. Students know variation within a species increases the likelihood that at least some members of a species will survive under changed environmental conditions.
8. Evolution is the result of genetic changes that occur in constantly changing environments. As a basis for understanding this concept:
a. Students know how natural selection determines the differential survival of groups of organisms.
b. Students know a great diversity of species increases the chance that at least some organisms survive major changes in the environment.
Protein synthesis comic strip: Created by teachers from the Science STARTS/Delta Sierra Science Program summer institute
Summary
Let your creative juices flow. The process of translating nucleic acids into amino acids becomes a tale of suspense, drama and adventure as you come up with a Marvel Comics style adventure story that is an analogy for protein synthesis. Draw comparisons between DNA and a secret message written in code. Compare ribosomes to factories churning out products. Students will surprise you with the crazy analogies they can come up with and the elegant stories they can spin.
Objectives
Reinforce and assess students’ understanding of the central dogma of molecular biology.
Vocabulary
DNA
Genetic code
Nucleotide
Base pair
RNA polymerase
Messenger RNA
Transfer RNA
Amino acid
Ribosome
Attachment | Size |
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Assess_comic.doc | 41 KB |
Time
30 min to introduce the activity. 1-3 hours to complete and present the comic strips.
Grouping
Individual
Materials
Setting
Classroom
Teacher Background
See background information from Protein Factory lesson.
Student Prerequisites
Good understanding of DNA structure (see DNA Models lesson) and protein synthesis (see Protein Factory lesson).
Getting Ready
Lesson Plan
Protein synthesis key concepts:
|
- “
DNAis located in thenucleusof thecell.”- “The sequence of
DNA nucleotidesforms thegenetic code.”
- “The mayor is located in the town hall of the city.”
- “A beautiful princess is located in the highest tower of the castle.”
- “The Pirate King is located on his pirate ship in the middle of the Black Sea.”
Sources
The inspiration for this assessment activity is the book The Cartoon Guide to Genetics by Larry Gonick and Mark Wheelis. It’s a wonderful textbook alternative that teaches genetics in a very entertaining, humorous way.
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
e. Students know DNA (deoxyribonucleic acid) is the genetic material of living organisms and is located in the chromosomes of each cell.
Grades 9-12
Cell Biology
1. The fundamental life processes of plants and animals depend on a variety of chemical reactions that occur in specialized areas of the organism's cells. As a basis for understanding this concept:
d. Students know the central dogma of molecular biology outlines the flow of information from transcription of ribonucleic acid (RNA) in the nucleus to translation of proteins on ribosomes in the cytoplasm.
Genetics
4. Genes are a set of instructions encoded in the DNA sequence of each organism that specify the sequence of amino acids in proteins characteristic of that organism. As a basis for understanding this concept:
a. Students know the general pathway by which ribosomes synthesize proteins, using tRNAs to translate genetic information in mRNA.
b. Students know how to apply the genetic coding rules to predict the sequence of amino acids from a sequence of codons in RNA.
e. Students know proteins can differ from one another in the number and sequence of amino acids.
Summary
The following are a series of real world genetics problems that relate to the genetic disorders cystic fibrosis and sickle cell anemia. They may be used to give students practice with Mendelian genetics and molecular biology or at the end of the unit to assess their understanding of various concepts.
Objectives
Reinforce and assess students understanding of real world genetics issues.
Attachment | Size |
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Assess_Real_World.doc | 42 KB |
Cystic Fibrosis
Cycstic fibrosis breathing apparatusCystic fibrosis is a genetic disease that affects many different parts of the body. There are approximately 30,000 Americans with cystic fibrosis. The most serious problem is the production of extremely thick, sticky mucus that clogs up the bronchial tubes in the lungs and the passageways in the pancreas (remember, the pancreas makes digestive juices that help break down food). This causes malnutrition, diabetes, lung infections, and difficulty getting enough oxygen to the body. Most people with cystic fibrosis die in their 20s or 30s from lung failure.
Cystic fibrosis is caused by a mutation in the cystic fibrosis gene. This gene provides the code for a protein that helps produce digestive juices and mucus.
CFTR geneCystic fibrosis is a recessive genetic disease. The normal allele can be represented by “G” and the mutant allele can be represented by “g”.
Cindy and Jonathan were married one year ago and are thinking of starting a family. Neither has cystic fibrosis. However, Cindy’s younger sister is very sick with cystic fibrosis. This has made Cindy and Jonathan worried that a baby they have together may be born with cystic fibrosis.
What are the chances that one of their kids is GG? ________%
What are the chances that one of their kids is Gg? ________%
What are the chances that one of their kids is gg? ________%
Cindy and Jonathan decide to get genetic testing to see whether either of them carries a mutant cystic fibrosis gene. Remember, Cindy and Jonathan do not have cystic fibrosis.
Sickle Cell Anemia
Sickle-shaped red blood cellsSickle cell disease is a disorder that affects the red blood cells. Red blood cells use a protein called hemoglobin to transport oxygen from the lungs to the rest of the body. Normally, red blood cells are round and flexible so they can travel freely through the narrow blood vessels.
Patients with sickle cell disease have a mutation in a gene that codes for part of the hemoglobin protein. As a result, hemoglobin does not form properly, causing red blood cells to be oddly shaped. These irregularly shaped cells get stuck in the blood vessels and are unable to transport oxygen properly, causing pain, frequent infections, and damage to the organs. Patients with sickle cell disease only survive to be 20 to 30 years old. About 1 in 500 babies born in America has the disease.
The normal hemoglobin nucleic acid sequence looks like:
T A C C A C G T G G A C T G A G G A C T C
A T G G T G C A C C T G A C T C C T G A G
Use the genetic code below to decode the top strand of the DNA.
Genetic Code
The mutant form of the hemoglobin gene is shown below with the mutation highlighted:
T A C C A C G T G G A C T G A G G A C A C
A T G G T G C A C C T G A C T C C T G T G
Sickle cell disease is a recessive genetic disease. The normal hemoglobin allele can be represented by “H” and the mutant allele can be represented by “h”.
Jack and Jill were married one year ago and are thinking of starting a family. Neither has sickle cell disease. However, Jack’s younger sister is very sick with sickle cell disease. This has made Jack and Jill worried that a baby they have together may be born with sickle cell disease. Jack and Jill decide to get genetic testing to see whether either of them has a mutant hemoglobin gene. The results come back saying that both Jack and Jill are both Hh.
Sickle cell disease is most common in people of African, Indian or Middle Eastern descent. Africa, India and the Middle East all have a big problem with another disease - malaria. If you get malaria, you become extremely sick with a high fever, vomiting, convulsions and possible organ failure. Infants and children are particularly vulnerable. Almost 1 million children die from malaria each year.
Interestingly, people that only have one copy of the mutant hemoglobin gene are more resistant to malaria. If infected, they become only slightly sick (with symptoms more like the common cold) and children that are heterozygous rarely die from malaria!
Summary
In this long term computer based simulation, students play with a fabulous FREE software program called Biologica developed by the Concord Consortium. It offers an in depth, virtual experience exploring Mendelian inheritance patterns in dragons. Activities increase in complexity from initial modules introducing dragons and their chromosomes to later activities that require problem solving skills and the integration of many levels of prior knowledge. In the program, you can manipulate dragon chromosomes, breed dragons, explore pedigrees, and more. There are fantastic puzzles along the way: Which gametes should you select to breed a purple, fire breathing, boy dragon? What happens if you change the DNA sequence? Can you figure out the genotype of invisible dragon parents from the phenotypes of their offspring?
Objectives
Can explain and use the relationship between genotype and phenotype to explain inheritance patterns.
Can take genotype information from 2 parents, model the creation of gametes by independent assortment, and use those gametes to create offspring.
Can explain the relationship between DNA, genes, and chromosomes.
Can explain how the inheritance of sex chromosomes contribute to an individual’s sex and to X-linked traits.
Can use Punnett squares to predict the possible allele combinations in the offspring given the genotypes of the parents.
Can understand the role of mutations in creating variation in phenotypes.
Vocabulary
Phenotype
Genotype
Gene
Allele
Chromosome
Dominant
Recessive
Incomplete dominance
Homozygous
Heterozygous
X linkage
Y chromosome
Meiosis
Gamete
Zygote
Punnett square
Monohybrid cross
Pedigree
Attachment | Size |
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Proj_Dragon_Genetics.doc | 49.5 KB |
Time
Students may spend anywhere between 1-8 hours playing with dragon genetics. There are 12 activities total. Each activity takes students between 20-50 minutes to complete depending on how quickly the child works. The full sequence is as follows:
It is not necessary or even recommended to complete every activity. My middle school students completed the abbreviated sequence below in 4 class periods. Students who finished early could continue on to the other activities.
Grouping
Individual although students working in pairs on the same computer is also fine.
Materials
Computer lab with at least one computer for every 2 students
Optional: For later modules, you may want to provide or have students create a paper “Dragon Genetics Rules” handout listing each of the traits and a phenotype to genotype translation (HH = horns, Hh = horns, hh = no horns).
Setting
Computer lab.
Teacher Background
My middle school students absolutely adored working on the program and begged me for more time to spend in the computer lab on it. The logical reasoning skills required in the advanced activities is quite sophisticated so use caution when requiring this program of students in 6th grade or below.
The Concord Consortium has created an excellent, downloadable teacher guide so see their materials for additional teacher background information. For questions about the software itself, see the Frequently Asked Questions area.
Student Prerequisites
None required although the first activity (Introduction) contains a whole lot of vocabulary. Therefore, I preferred introducing Dragon Genetics after students had been introduced to genes, alleles, and simple dominance (see Making Babies Lab).
Getting Ready
Lesson Plan
Assessment
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
b. Students know sexual reproduction produces offspring that inherit half their genes from each parent.
c. Students know an inherited trait can be determined by one or more genes.
d. Students know plant and animal cells contain many thousands of different genes and typically have two copies of every gene. The two copies (or alleles) of the gene may or may not be identical, and one may be dominant in determining the phenotype while the other is recessive.
e. Students know DNA (deoxyribonucleic acid) is the genetic material of living organisms and is located in the chromosomes of each cell.
Grades 9-12
Genetics
2. Mutation and sexual reproduction lead to genetic variation in a population. As a basis for understanding this concept:
a. Students know meiosis is an early step in sexual reproduction in which the pairs of chromosomes separate and segregate randomly during cell division to produce gametes containing one chromosome of each type.
b. Students know only certain cells in a multicellular organism undergo meiosis.
c. Students know how random chromosome segregation explains the probability that a particular allele will be in a gamete.
d. Students know new combinations of alleles may be generated in a zygote through the fusion of male and female gametes (fertilization).
e. Students know why approximately half of an individual's DNA sequence comes from each parent.
f. Students know the role of chromosomes in determining an individual's sex.
g. Students know how to predict possible combinations of alleles in a zygote from the genetic makeup of the parents.
3. A multicellular organism develops from a single zygote, and its phenotype depends on its genotype, which is established at fertilization. As a basis for understanding this concept:
a. Students know how to predict the probable outcome of phenotypes in a genetic cross from the genotypes of the parents and mode of inheritance (autosomal or X-linked, dominant or recessive).
b. Students know the genetic basis for Mendel's laws of segregation and independent assortment.
c. * Students know how to predict the probable mode of inheritance from a pedigree diagram showing phenotypes.
Summary
Variation in a population is the raw material on which natural selection works. How do scientists measure and quantify variation in traits? We use garden snails as a model organism in order to describe and measure several different traits. Groups are given a small population of snails and must devise an objective way to measure a trait of their choosing (length, mass, speed, color intensity, stripes, withdrawal reflex reaction time, number of pennies it can carry, etc.). There are many ways to extend this activity. For instance, scientific protocols may be traded between groups, hypotheses may be made concerning what individuals will survive better in different environments, and snails may be tagged and released into one or more environments and the populations monitored over time. A long term open-ended project such as this provides a natural extension and assessment opportunity for both evolution and ecology concepts.
Objectives
Can make observations in an objective, quantifiable manner.
Can select and use tools to collect data.
Can use tables and graphs to represent data and identify patterns in data.
Can describe the role of variation in a population in natural selection and evolution.
Vocabulary
Traits
Variation
Population
Natural selection
Evolution
Objective
Subjective
Quantify
Histogram
Attachment | Size |
---|---|
Proj_Snail_Variations.doc | 47 KB |
Time
50 minutes to measure, quantify, and discuss variation in snail traits. The extension projects described in the Going Further section may last several months.
Grouping
Teams of 3-4 students.
Materials
For each group of 3-4 students you need:
Other supplies you may want on hand for groups to share:
Setting
Initial measurement of snail traits can be done in the classroom. Extension projects should be done in a schoolyard, garden, creek, park or other local outdoor area that has a resident snail population – ideally, this is the location where the snails were collected.
Teacher Background
Natural selection and evolution are core ideas in biology and, in fact, all of science. Natural selection can briefly be described the process by which those individuals whose traits best fit their environment are most likely to survive, reproduce, and pass their genes on to the next generation. One of the critical “raw ingredients” of natural selection is variation in a population. All natural populations (groups of organisms of the same species) vary in their traits based on the interplay between genetics and environmental factors.
This activity uses the common garden snail (Helix aspersa) to measure variations in a population. These animals are garden pests found throughout North America and are readily captured from around most neighborhoods in California. I generally pay my neighbor’s kids 5¢ a snail and end up with upwards of 40 snails in less than an hour.
Snails are incredibly easy to keep in the classroom. They can survive in the classroom almost indefinitely with regular feeding and cleaning. Keep snails in a plastic shoebox or glass terrarium. Keep the terrarium covered securely while letting in air for them to breathe. Snails are strong and can easily push off a plastic lid, so secure the lid with rubber bands if necessary. Stock their habitat with several wet paper towels and vegetables from the grocery store (lettuce, carrots, apples, etc.). Twice a week, clean out their habitat by throwing away the old paper towels and food and giving them new wet paper towels and food. If you are keeping the snails longer than a week, place pieces of chalk in each container since they need calcium for shell growth and repair.
At the end of your project, snails may be released if they were collected locally. It is often interesting to “tag” the snails before you release them with a dot of nail polish on their shells. Thus, individuals may be tracked over time. If you choose not to release these pests back into your neighbors’ gardens, they may be frozen then thrown away. The adventurous can try cooking and eating them. That’s right! The garden snails found in North America are the same species that is used in escargot. In the going further section, there are resources for how to make escargot – although beware… this may be traumatic to some of your students.
Student Prerequisites
None required although familiarity with observation, measurement, and histograms is helpful (see Human Traits Survey lesson).
Getting Ready
Lesson Plan
Assessment
Going Further
Sources
This lesson was adapted from a lesson by Karen Kalamuck of the Exploratorium Teachers Institute.
For information on snails and snail care, see this website from the Lawrence Hall of Science.
The escargot recipe is taken from Gourmet Magazine, March 2001. A copy of this can be found at Epicurious.com.
Standards
Grade 7
Evolution
3. Biological evolution accounts for the diversity of species developed through gradual processes over many generations. As a basis for understanding this concept:
a. Students know both genetic variation and environmental factors are causes of evolution and diversity of organisms.
Investigation and Experimentation
7. Scientific progress is made by asking meaningful questions and conducting careful investigations. As a basis for understanding this concept and addressing the content in the other three strands, students should develop their own questions and perform investigations. Students will:
a. Select and use appropriate tools and technology (including calculators, computers, balances, spring scales, microscopes, and binoculars) to perform tests, collect data, and display data.
e. Communicate the steps and results from an investigation in written reports and oral presentations.
Grade 9-12
Evolution
7. The frequency of an allele in a gene pool of a population depends on many factors and may be stable or unstable over time. As a basis for understanding this concept:
a. Students know why natural selection acts on the phenotype rather than the genotype of an organism.
8. Evolution is the result of genetic changes that occur in constantly changing environments. As a basis for understanding this concept:
a. Students know how natural selection determines the differential survival of groups of organisms.
b. Students know a great diversity of species increases the chance that at least some organisms survive major changes in the environment.
Investigation and Experimentation
1. Scientific progress is made by asking meaningful questions and conducting careful investigations. As a basis for understanding this concept and addressing the content in the other four strands, students should develop their own questions and perform investigations. Students will:
a. Select and use appropriate tools and technology (such as computer-linked probes, spreadsheets, and graphing calculators) to perform tests, collect data, analyze relationships, and display data.
b. Identify and communicate sources of unavoidable experimental error.
c. Identify possible reasons for inconsistent results, such as sources of error or uncontrolled conditions.
Summary
Students create DNA models from beads and wire that may be used as earrings, pendants, Christmas ornaments, and/or key chain pulls. This project is simple enough that a good substitute could lead the students through it since the content should be taught beforehand. More importantly, this is just one of many possible 3D DNA models you could have your students build. Be creative! Use gumdrops, Styrofoam, marshmallows, Legos, grapes, wood, aluminum cans, etc. Better yet, have your students design a model independently.
Objectives
Reinforce student understanding of the general structure of DNA and base pairing rules.
Vocabulary
DNA
Deoxyribose
Phosphate
Nucleic acid
Adenine
Thymine
Cytosine
Guanine
Base pairs
Nucleotide
Attachment | Size |
---|---|
Sub_DNA_Jewelry.doc | 71.5 KB |
Sub_DNA_Jewelry.pdf | 65.68 KB |
Time
45-50 minutes
Grouping
Individual
Materials
Each student needs:
Groups of 4-6 students need:
Setting
Classroom
Teacher Background
See Teacher Background in Paper DNA Models Lesson.
Student Prerequisites
Good understanding of DNA structure. See Paper DNA Models Lesson.
Getting Ready
Instructions
Sources
This activity was adapted from a DNA earring design by Karen Kalamuck of the Exploratorium Teacher Institute and from the “Modeling DNA, the Code of Life” activity by the RAFT Education Department. I recently discovered another write up for this activity by Catherine Ross .
Standards
Grade 7
Genetics
2. A typical cell of any organism contains genetic instructions that specify its traits. Those traits may be modified by environmental influences. As a basis for understanding this concept:
e. Students know DNA (deoxyribonucleic acid) is the genetic material of living organisms and is located in the chromosomes of each cell.
Grades 9-12
Genetics
5. The genetic composition of cells can be altered by incorporation of exogenous DNA into the cells. As a basis for understanding this concept:
a. Students know the general structures and functions of DNA, RNA, and protein.
Students know how to apply base-pairing rules to explain precise copying of DNA during semiconservative replication and transcription of information from DNA into mRNA.