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High-Throughput Genotyping With Energy Transfer-Labeled Primers

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Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 335))

Abstract

The Amplifluor method for single-nucleotide polymorphisms (SNP) genotyping provides homogeneous assays that utilize a pair of universal energy transfer-labeled primers. The main advantage of this single-step, loci-independent, low-cost method is that it can be readily adapted for new SNPs. The development of any new SNP assay requires only the design and synthesis of three conventional oligonucleotides. Furthermore, Amplifluor-based SNP assays require instrumentation found in most laboratories including a thermocyler and fluorescent plate-reader. Here, we provide detailed protocols for primer design, both manually and using AssayArchitectTM software. Protocols for SNP analysis are provided along with more than 100 examples for common polymorphisms. Specific cases including polymorphisms caused by the insertion/deletion of nucleotides, and dealing with the AT- and GC-rich sequences are addressed and discussed in detail.

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References

  1. Brookes, A. (1999) The essence of SNPs. Gene 234, 177–186.

    Article  PubMed  CAS  Google Scholar 

  2. Roses, A. (2000) Pharmacogenetics and the practice of medicine. Nature 405, 857–865.

    Article  PubMed  CAS  Google Scholar 

  3. Weiss, K. and Terwilliger, J. (2000) How many diseases does it take to map a gene with SNPs? Nature Genet. 26, 151–157.

    Google Scholar 

  4. McCarthy, J. and Hilfiker, R. (2000) The use of single-nucleotide polymorphism maps in pharmacogenomics. Nat. Biotechnol. 18, 505.

    Article  PubMed  CAS  Google Scholar 

  5. Nebert, D. W. (1999) Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist? Clin. Genet. 56, 247–258.

    Article  PubMed  CAS  Google Scholar 

  6. Gray, I. C., Campbell, D. A., and Spurr, N. K. (2000) Single nucleotide polymorphysms as tools in human genetics. Hum. Mol. Genet. 9, 2403–2408.

    Article  PubMed  CAS  Google Scholar 

  7. Livak, K. J. (1999) Allelic discrimination using fluorogenic probes and the 5¢ nuclease assay. Genet. Anal. 14, 143–149.

    PubMed  CAS  Google Scholar 

  8. Tyagi, S., Bratu, D. P., and Kramer, F. R. (1998) Multicolor molecular beacons for allele discrimination. Nat. Biotechnol. 16, 49–53.

    Article  PubMed  CAS  Google Scholar 

  9. Myakishev, M. Y., Khripin, Y., Hu, S., and Hamer, D. (2001) High throughput SNP genotyping by allele-specific PCR with universal energy transfer-labeled primers. Genome Res. 11, 163–169.

    Article  PubMed  CAS  Google Scholar 

  10. Hawkins, J. R., Khripin, Y., Valdes, A. M., and Weaver, T. A. (2002) Miniaturized sealed-tube allele-specific PCR. Human Mutation. 19, 543–553.

    Article  PubMed  CAS  Google Scholar 

  11. Bengra, C., Mifflin, T. E., Khripin, Y., et al. (2002) Genotyping of essential hypertension single nucleotide polymorphisms by a homogeneous PCR method with universal energy transfer primers. Clin. Chem. 48, 2131–2140.

    PubMed  CAS  Google Scholar 

  12. Okayama, H., Curiel, D. T., Brantly, M. L., Holmes, M. D., and R. Crystal, R. D. (1989) Rapid, nonradioactive detection of mutations in human genome by allelespecific amplification. J. Lab. Clin. Med. 114, 105–113.

    PubMed  CAS  Google Scholar 

  13. Newton, C. R., Graham, A., Heptinstall, L. E., et al. (1989) Analysis of any point mutation in DNA. The amplification of refractory mutation systems (ARMS). Nucleic Acids Res. 17, 2503–2516.

    Article  PubMed  CAS  Google Scholar 

  14. Nazarenko, I. A., Bhatnagar, S. K., and Hohman, R. J. (1997) A closed tube format for amplification and detection of DNA based on energy transfer. Nucleic Acids Res. 25, 2516–2521.

    Article  PubMed  CAS  Google Scholar 

  15. Chester, N. and Marshak, D. R. (1993) Dimethyl sulfoxide-mediated primer Tm reduction: a method for analyzing the role of renaturation temperature in the polymerase chain reaction. Anal. Biochem. 209, 284–290.

    Article  PubMed  CAS  Google Scholar 

  16. Rychlik, W. (1995) Priming efficiency in PCR. Biotechniques 18, 84–90.

    PubMed  CAS  Google Scholar 

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© 2006 Humana Press Inc., Totowa, NJ

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Khripin, Y. (2006). High-Throughput Genotyping With Energy Transfer-Labeled Primers. In: Didenko, V.V. (eds) Fluorescent Energy Transfer Nucleic Acid Probes. Methods in Molecular Biology™, vol 335. Humana Press. https://doi.org/10.1385/1-59745-069-3:215

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  • DOI: https://doi.org/10.1385/1-59745-069-3:215

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-58829-380-0

  • Online ISBN: 978-1-59745-069-0

  • eBook Packages: Springer Protocols

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