1 / 11

DNA Polymorphisms: DNA markers a useful tool in biotechnology

DNA Polymorphisms: DNA markers a useful tool in biotechnology. Any section of DNA that varies among individuals in a population, “many forms”. Examples include: SNPs, RFLPs, STRPs, and AFLPs; RFLPs include VNTRs and STRPs microsatellites (STRs) = SSLPs = STRPs = SSRs

Download Presentation

DNA Polymorphisms: DNA markers a useful tool in biotechnology

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. DNA Polymorphisms: DNA markers a useful tool in biotechnology • Any section of DNA that varies among individuals in a population, “many forms”. • Examples include: SNPs, RFLPs, STRPs, and AFLPs; • RFLPs include VNTRs and STRPs • microsatellites (STRs) = SSLPs = STRPs = SSRs • Useful for finding, mapping genes involved in disease, and • Individual identification, epidemiology, anthropology, population/ecology studies, taxonomy.

  2. SNPs Single nucleotide polymorphisms: regions of DNA where one base pair is different. Occur evenly spread over all the DNA. 1/ 1000-3000 bp Detected by sequencing. If SNP occurs in a restriction enzyme site, it generates an RFLP. Could be in coding or non-coding regions. Over 300,000 human SNPs known and are being mapped.

  3. SNP

  4. RFLPs Restriction fragment length polymorphism. Mutation at a restriction site prevents recognition & cutting. Results in one band of larger DNA instead of 2 smaller ones. scidiv.bcc.ctc.edu/.../lectures/ DNATechnology/image021.jpg

  5. Other RFLPs: VNTRs and STRPsMinisatellites and Microsatellites • These are RFLPs because they are defined by or visible following restriction enzyme cuts. • Variable Number Tandem Repeats • Groups (10-100) of nucleotides repeated 2 – 100 times (depending on individual and locus). • Restriction sites on both sides of repeated DNA • The more repeats, the longer the fragment. • Simple Tandem Repeat Polymorphisms • Shorter, 2-9 nucleotides repeated • Small enough number for PCR amplification • Also called STRs, SSLPs, etc.

  6. Use of VNTRs Restriction sites are on either side; fragment length depends on number of repeats in between sites.

  7. STRPs Primers for both sides of repeated region allow PCR amplification of DNA; generates PCR products that differ in length depending on number of repeats. Becoming the standard method for DNA testing in forensics labs. Cheaper, easier, more sensitive.

  8. STRs in forensics Locus vWA • 14 0.081 • 15 0.107 • 15.2 0.179 • 16 0.306 • 17 0.192 • 18 0.089 • 19 0.047 Alleles in different ethnic and racial groups examined, used as database. Panel of 13 different STRs are used. Because the odds of a particular combination of the 13 is product of the frequencies, numbers like 1 in 10 billion can be generated. Band frequency

  9. THE 13 CODIS STRs http://expertpages.com/news/dna.htm

  10. RAPD: using PCR to find polymorphisms “Random amplified polymorphic DNA” Screen DNA from individuals by doing PCR with random short primers. By random chance, primers will amplify many different sections of DNA. Look for bands on gel that are not present in each individual tested. avery.rutgers.edu/.../ archives/onions/rapd.html

  11. RAPD: using PCR to find polymorphisms-2

More Related