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TE Activity: DNA Build Contributed by: Integrated Teaching and Learning Program, College of Engineering, University of Colorado at Boulder
Pre-Req Knowledge (Return to Contents) An understanding that DNA is the genetic material for all living things. Learning Objectives (Return to Contents) After this activity, students should be able to:
Materials List (Return to Contents) Each group needs:
For the entire class to share:
Introduction/Motivation (Return to Contents) We have all heard about DNA, but what exactly is DNA and why is it important to us? DNA stands for deoxyribonucleic acid and is made up of billions of biochemicals. DNA is the genetic material for all living things — this means that you, me, flowers, dogs, elephants and even viruses contain DNA. You can think of DNA as the "recipe" for living things — it provides the instructions for every part of the organism. In humans, 99.99% of our DNA is exactly the same as every other person's. Why is there a 0.01% difference? This small amount of DNA is what determines our physical differences such as eye color, hair color, height, etc. Even though our DNA is almost all the same, every single person (except for identical twins) has a unique DNA "recipe." Where in our bodies is DNA located? DNA is stored in the nucleus of each cell where it is best protected from damage. Each nucleus contains 23 pairs (23 from your mom and 23 from your dad) of DNA, called chromosomes. This DNA is folded over and over into VERY small bundles — much too small for the human eye to see. DNA is organized into shorter segments called genes. Think about a gummy candy worm as the entire strand of DNA, but each colored segment is a different gene. Genes are specific sequences of DNA that code for certain characteristics. The DNA sequence is called the genotype — this is the recipe — and the characteristics are called the phenotype — this is the cake! DNA is made of four biochemicals called nucleotide bases (or just "bases"). Think of these as the ingredients in the recipe. They are: adenine, thymine, guanine and cytosine. To make things easier, people usually abbreviate these as A, T, G and C. These four bases pair with each other in a very specific way: A always pairs with T and G always pairs with C. One gene usually contains 10,000 to 15,000 base pairs!
Why is it important to understand genes and base pair sequences? Have you ever heard of color blindness, Down syndrome, cystic fibrosis or hemophilia? Well, biomedical engineers work with others in the scientific and medical fields to help improve health care and quality of life. They study DNA to help us understand genetic disorders like these. As engineers develop technologies to recognize certain DNA mutations and where they are located, they work with geneticists to diagnose, treat and prevent these disorders. Genetic engineers study genes and DNA to understand things like DNA replication, cloning and genetically-modified organisms such as food and crops. Genetic engineers have helped us advance our crop technologies and make synthetic (artificial) insulin for people with diabetes. DNA can also identify people — even better than fingerprints. DNA is found in all of our cells: hair, teeth, bones, blood and saliva. We can leave our DNA behind when we drink from a cup, use a toothbrush, shed hair or cut ourselves on something sharp. Because of this, DNA is used for "DNA fingerprinting" — or describing the unique DNA recipe for a person. Even 0.01% difference is enough to distinguish one person from another when it comes to collecting evidence from a crime scene. Using DNA in a crime investigation does have its limitations. The probability of laboratory error or contamination — errors made when collecting and running the DNA samples — must be factored into the results. It is always best to consider DNA fingerprinting along with other evidence. Biomedical engineers create the tools, equipment and processes to accurately collect and examine DNA evidence for crime and paternity cases. They are always working to make the laboratory errors fewer and the machines for identifying the gene sequences more accurate. Today, we are going to practice determining the phenotypes (physical characteristics) of persons from their DNA. We are going to work together to make models of human DNA and swap them with each other to decode. Like biomedical engineers, let's break down DNA gene sequences into individual traits to describe the people to which the DNA belongs. Vocabulary/Definitions (Return to Contents)
Procedure (Return to Contents) Background Remind students that DNA is composed of four nucleotide bases: adenine (A), thymine (T), guanine (G) and cytosine (C). These four bases pair with each other in a very specific way: A always pairs with T and G always pairs with C. Before the Activity
With the Students: Part 1
Suggested DNA Building Steps It is easiest to construct the DNA strand by following these steps:
With the Students: Part 2
Attachments (Return to Contents)
Troubleshooting Tips (Return to Contents) Groups may need to trade with other groups from their given gumdrop supply, as the gumdrop colors are different on each color key. When connecting all the genes together, be sure to keep the genes in the correct order and orientation, or else they won't be able to be decoded by another team. Assessment (Return to Contents) Pre-Activity Assessment Discussion Questions: Ask the students and discuss as a class.
Activity Embedded Assessment Question/Answer: While students are building their DNA strands, ask them the following questions:
Post-Activity Assessment Biomedical Engineering and Genetic Disorders Discussion: Most genetic disorders are associated with an alteration of DNA. For example, color blindness can be associated with a single mutation (change) on any of 19 different chromosomes and multiple different genes. These genetic disorders can be either numerical or structural. Numerical disorders occur when a DNA chromosome is either missing or has an extra copy. For example, Down syndrome is an example in which three copies of a DNA chromosome exist, instead of two. Structural disorders occur when a portion of a DNA chromosome is missing or replicated or moved to the wrong place. Have students discuss how an engineer might be able to develop technologies that look for specific gene changes or mutations in DNA. Using the color key, which of the following DNA samples might have a genetic disorder? What is the alteration? (Note: None of the following examples result in real disorders, but they each illustrate a type of change in the gene sequence of the DNA piece.)
Activity Extensions (Return to Contents) Have students research a specific genetic disorder and write a one-page summary about it, including a description of which chromosome is affected and the associated mutation. Examples include Down syndrome, color blindness, hemophilia and cystic fibrosis. Activity Scaling (Return to Contents)
References (Return to Contents) About R&D - Research & Development. Updated November 27, 2008. GlaxoSmithKline plc. Accessed March 2, 2009. http://www.genetics.gsk.com/kids/dna01.htm Bachor, Kevin. Fun Facts (about DNA). The Best Detergent for Plentiful DNA Extraction, Cirque du Soleil, Ecole Nationale de Cirque, 2006 Canada Wide Virtual Science Fair. Accessed March 2, 2009. http://www.virtualsciencefair.org/2006/bach6k2/Funfacts.htm Contributors Megan Schroeder, Malinda Schaefer Zarske, Janet Yowell, Denise W. CarlsonCopyright © 2007 by Regents of the University of Colorado. This digital library content was developed by the Integrated Teaching and Learning Program under National Science Foundation GK-12 grant no. 0338326. However, these contents do not necessarily represent the policies of the National Science Foundation, and you should not assume endorsement by the federal government.Supporting Program (Return to Contents) Integrated Teaching and Learning Program, College of Engineering, University of Colorado at BoulderLast Modified: August 10, 2010
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