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Wiki - DNA Fingerprinting, Individual Identification and Ancestry | Coursera Link Your Coursework to Your Identity 14/07/2014 × Get Started Courses Genetics and Society: A Course for Educators by Rob DeSalle, Ph.D., David Randle, Ph.D. Dana Taylor Join Signature Track 2 days and 5 hours left DNA Fingerprinting, Individual Identification and Ancestry Help By Dr. Claudia Englbrecht (Guest Author) COURSE Announcements Syllabus & Grading Policy Course Checklist Surveys Map WEEKLY CONTENT Week 1 Week 2 QUIZZES & ASSIGNMENTS Genetic fingerprinting, a molecular technology that allows individuals to be identified based on their DNA, has become central to forensics, paternity testing, conservation biology, evolutionary biology and ancestry research. It would be hard to find a television episode of CSI that doesn't mention this technology. But what is a genetic or DNA fingerprint? How accurate are they? How much information about an individual does a genetic fingerprint actually hold? In the 1980s, well before the Genomic Revolution, researchers discovered that our genomes contain large amounts of so called "repetitive DNA." In thousands of locations, basic short motifs like GA or CAG are repeated in our genetic code, to read something like GAGAGAGAGA or CAGCAGCAGCAG — a "genome stutter". The key to the diagnostic power of a genetic fingerprint lies in understanding these repetitive elements, which are called microsatellites or short tandem repeats (STRs). In principle microsatellites behave like genes. Let's say that Location X on Chromosome 1 harbors a microsatellite. We have two copies of Chromosome 1 and therefore we also have two copies of the microsatellite. Both copies have the same core sequence, e.g. GA, but they can have different numbers of repeats. One copy could have five repeat units, GAGAGAGAGA, and the other copy could have eight repeats, GAGAGAGAGAGAGAGA. Unlike genes that can vary in sequence, the repetitive elements can (but do not have to) vary in the number of repeat units. Quizzes Assignment RESOURCES In the Classroom COMMUNITY Discussion Forums @ AMNH Opportunities for Educators So why are microsatellites so useful for individual identifications? Why not use genes that code for blood type or hair color? Microsatellites have another important characteristic: they are extremely variable. For some of them we can find up to 20 or more different length variants in the human population; the core repeat unit may be replicated four, six, eight, ten times, or more. Most single copy genes in our genome are much less variable and only come in a limited number of versions (alleles); for example, the gene that determines your blood type exists as just three different alleles: A, B and O. Each individual can harbor only a maximum of two different length variants per microsatellite analogous to two alleles in single gene copies. You can see that microsatellites have a higher power of resolution than, for instance, the alleles for blood groups. The probability that you have the same two length versions at a microsatellite locus as your neighbor is lower than the probability that you share the same blood type, because there are more microsatellite variations in the population. Detecting Microsatellite Markers This microsatellite consists of tandem repeats of the dinucleotide CA. The number of repeats in such microsatellites varies with the individual (for example: four repeats in individual I and eight repeats in individual II). These variations can be detected by PCR amplification with primers that flank the repeat region, since this process yields amplified DNA products of different lengths. ©NIH Support AMNH MEET UP Join a Meetup Compare this to a lottery in which you pick two numbers out of a pool. If the pool contains only three numbers, the likelihood of other people picking the same two numbers is high. If the pool contains 20 numbers, it's far less likely that somebody else will get the same number as you. Microsatellites offer geneticists a large pool of markers across which to establish a match. Help Articles Course Materials Errors Technical Issues However, examining just one microsatellite locus is not sufficient to make DNA profiling unambiguous - especially in a death penalty case. There is still a chance that you and your neighbor have the same two microsatellite-length variations. A forensic DNA profile is reliable because several different microsatellite loci are studied at any given time, and because geneticists have compiled databases of the frequencies of microsatellite versions across human populations. Consider the same lottery, but imagine that you had ten opportunities to pick two 2 numbers out of a pool of 20. The probability that you and another person would choose the exact same numbers all 10 times is extremely low. But you cannot go to court and say, "The probability is extremely low, so the suspect has to be convicted." Forensic scientists must present solid statistics that yield exact probabilities. Their statistics are https://class.coursera.org/amnhgenetics-003/wiki/view?page=DNA_Fingerprinting 1/3 Wiki - DNA Fingerprinting, Individual Identification and Ancestry | Coursera 14/07/2014 based on those population databases. Without pre-existing data on these frequency distributions, we could not assign a reliable probability value to any DNA fingerprint. The probability of any two individuals having an exact match in the microsatellite combinations used in forensics is typically something like one in several billion. This is why courts of law allow DNA profiling to identify people. Conversely, if a suspect's DNA does not match that found at a crime scene, it is immediately clear that he or she did not do it. One criticism of the use of DNA fingerprints is the data underlying the probability calculations. Is the database really representative of the population? If not, the calculated probability values will be biased. However, the biases are known and are taken into consideration. A typical genetic fingerprint, which looks on average at ten different microsatellites, does not reveal anything about your personality, your mental capabilities, your ethnicity or possible predispositions to disease. However, exhaustive studies on human populations from all over the world have shown that if we look at a far larger number of specific microsatellites (several hundred), we can roughly determine that individual's ancestry. How is that possible if humans are genetically so similar, you might ask? This is because the worldwide distribution of certain alleles is uneven. For example length variant 1 could be very common in Central Africa, but less so in Asia and Northern Europe, while length variant 2 could be more abundant in Northern Europe than anywhere else, and so forth. The uneven distribution is due to the evolutionary history of modern humans, who migrated from Africa through the Middle East and on across the other continents. Nowadays, we have large sets of microsatellite data (and of other genetically informative elements). We also know a lot about the genetic variability of populations around the world. Most alleles are widespread. Only very few alleles occur in specific regions and are genuinely rare. The map of human genetic variation also shows that there are no abrupt changes in frequencies, but rather continuous, gradual changes between populations and continents. DNA tests are a very powerful tool inside and outside the courtroom. Inevitably, they involve serious ethical and legal issues. Is DNA fingerprinting really the perfect evidence? Are the results always accurate? Who should be in these databases? Only convicts, people under arrest or the entire population? Would you want your DNA profile in a large database or would you prefer to keep your genetic profile private? Related Resources Rosenberg, Noah A., et al. "Genetic Structure of Human Populations." Science 298 (20 December 2002): 2381-2385. Witherspoon, D.J., et al. "Genetic Similarities Within and Between Human Populations." Genetics 176 (May 2007): 351-359. Related Links DNA on the Witness Stand » Dr. Eric Lander, director of the Center for Genome Research at MIT, examines how genetics affects forensics in civil and criminal court cases. As you scroll through the pages, you will learn about genetic individuality, how DNA is used for forensic purposes, and the controversial proposal of a genetic database. DNA Learning Center » Explore these animations to learn about the procedure for making and reading a DNA fingerprint, and read three cases that illustrate the process. Confusions About Human Races » Read this article from Harvard University professor Richard Lewontin on race and genomics. Forensic Mathematics of DNA Matching » Understand the calculation of DNA profile probabilities and what they mean. Combined DNA Index System » Get an overview on the laboratory procedures used by the Federal Bureau of Investigations for forensic DNA evidence. https://class.coursera.org/amnhgenetics-003/wiki/view?page=DNA_Fingerprinting 2/3 Wiki - DNA Fingerprinting, Individual Identification and Ancestry | Coursera 14/07/2014 Created Tue 16 Jul 2013 2:58 PM UTC Last Modified Tue 1 Jul 2014 5:33 PM UTC https://class.coursera.org/amnhgenetics-003/wiki/view?page=DNA_Fingerprinting 3/3