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Investigations to Improve Allele Definition in the “Collagen 2A1” System (AMP-FLP)

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Advances in Forensic Haemogenetics

Part of the book series: Advances in Forensic Haemogenetics ((HAEMOGENETICS,volume 4))

Abstract

Continuous distributions of fragments are still characteristic of the highly polymorphic single locus VNTR systems (Puers et al. 1991). To solve these problems different bin approaches and match criteria have been elaborated (Baird et al. 1986, Brenner and Morris 1990, Gill et al. 1990). Another inherent problem lies in the use of λ-DNA as marker DNA whose sequences differ considerably from those to be measured. The electrophoretic mobility of DNA is also influenced by sequence and composition. Therefore, λ-DNA is basically not suitable for estimating size of (human) fragments. One concept for a more exact estimation of allele size is to compare the unknown human fragment with a human DNA standard composed of as many alleles from the system under investigation as possible (Puers et al. 1991).

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References

  • Baird M, Balazc I, Giusti A, Miyazaki L, Nicholas L, Wexler K, Kanter E, Glassberg J, Allen F, Rubinstein, P. and Sussman, L. (1986) Allele frequency distribution to two highly polymorphic DNA sequences in three ethnic groups and its application to the determination of paternity. Am J Hum Genet, 29, 489–501

    Google Scholar 

  • Brenner C and Morris JW (1990) Paternity index calculations in single locus hypervariable DNA probes: Validation and other studies. The International Symposium on Human Identification - published by Promega Corporation, 219–55

    Google Scholar 

  • Brinkmann B, Rand Sand Wiegand P (1991) Population and family data of RFLP’s using sleeted single - and multilocus systems, Int J Leg Med 104: 819–86

    Article  CAS  Google Scholar 

  • Budowle B, Chakraborty R, Giusti AM, Eisenberg AJ and Allen RC (1991) Analysis of the variable numer of tandem repeat locus D1S80 by the polymerase chain reaction followed by high resolution polyacrylamide gel elctrophoresis. Am J Hum Genet 48: 1379–144

    PubMed  CAS  Google Scholar 

  • Gill, P., Sullivan, K. and Werrett, D.J. (1990) The analysis of hypervariable DNA profiles: problems associated with the objective determination of the probability of a match. Hum Genet 85: 759–79

    Article  PubMed  CAS  Google Scholar 

  • Nakamura Y., Leppert M., O’Connell P., Wolff R., Holm T., Culver M., Martin C., Fujimoto E., Hoff M., Kulmin E. and White R. (1987a) Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 235: 16169–1622

    Article  PubMed  CAS  Google Scholar 

  • Nakamura Y, Gillilan S, O’Connell P, Leppert M, Lathrop GM, Lalouel J-M, White R (1987b) Isolation and mapping of a polmorphic DNA sequence pYNH24 on chromosome 2 (D2S44). Nucleic Acids Res 15: 10073

    Article  PubMed  CAS  Google Scholar 

  • Puers C, Rand S and Brinkmann B (1991) Concept for a more precise definition of the polymorphism YNH24. In: Berghaus G, Brinkmann B, Rittner C and Staak M (eds.), DNA-technology and its forensic application, Springer Verlag/Heidelberg (in press)

    Google Scholar 

  • Priestley L, Kumar D and Sykes B (1990) Amplification of the COL2A1 3′variable region used for segregation analysis in a family with Stickler syndrome. Hum Genet 85: 5259–526

    Article  PubMed  CAS  Google Scholar 

  • Stoker NG, Cheah KS, Griffin JR, Pope FM and Solomon E (1985) A highly polymorphic region 3′ to the human type II collagen gene. Nucleic Acids Res 13: 46139–4622

    Article  PubMed  CAS  Google Scholar 

  • Wu S, Seino S and Bell GI (1990) Human collagen, type II, alpha 21, (COL2A1) gene: VNTR polymorphism detected by gene amplification. Nucleic Acids Res 18: 3102

    Article  PubMed  CAS  Google Scholar 

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© 1992 Springer-Verlag Berlin Heidelberg

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Puers, C., Wiegand, P., Brinkmann, B. (1992). Investigations to Improve Allele Definition in the “Collagen 2A1” System (AMP-FLP). In: Rittner, C., Schneider, P.M. (eds) Advances in Forensic Haemogenetics. Advances in Forensic Haemogenetics, vol 4. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77324-2_6

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  • DOI: https://doi.org/10.1007/978-3-642-77324-2_6

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-55194-2

  • Online ISBN: 978-3-642-77324-2

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