Literature DB >> 11005174

A rare mutation in the amelogenin gene and its potential investigative ramifications.

P E Roffey1, C I Eckhoff, J L Kuhl.   

Abstract

Over the past few years, the Australian forensic science community has adopted a common methodology and technology in the application of DNA profiling for investigative and forensic purposes. The ultimate objective of this initiative is the establishment of a national DNA database similar to that used in the UK. An integral part of this methodology is the use of "Profiler Plus," a nonaplex of STRs combined with amelogenin, a locus utilized for sex determination. This paper reports the results from a case where a mutation in the annealing region of the amelogenin primers appears to have resulted in the failure to amplify the amelogenin Y-homolog from a phenotypically normal male. The result was confirmed using two different primer sets that amplify different regions of the amelogenin gene. This situation suggests that the genetic determination of sex based on the amelogenin sequences from specimens of unknown origin, such as crime scene samples, should not be considered infallible.

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Year:  2000        PMID: 11005174

Source DB:  PubMed          Journal:  J Forensic Sci        ISSN: 0022-1198            Impact factor:   1.832


  10 in total

1.  Rare failures in the amelogenin sex test.

Authors:  M Steinlechner; B Berger; H Niederstätter; W Parson
Journal:  Int J Legal Med       Date:  2002-04       Impact factor: 2.686

2.  A rare mutation in the primer binding region of the amelogenin gene can interfere with gender identification.

Authors:  Bonnie Shadrach; Mairead Commane; Carol Hren; Ilka Warshawsky
Journal:  J Mol Diagn       Date:  2004-11       Impact factor: 5.568

3.  Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations.

Authors:  Rita Y Y Yong; Linda S H Gan; Yuet Meng Chang; Eric P H Yap
Journal:  Hum Genet       Date:  2007-06-23       Impact factor: 4.132

4.  "GenderPlex" a PCR multiplex for reliable gender determination of degraded human DNA samples and complex gender constellations.

Authors:  Anna Esteve Codina; Harald Niederstätter; Walther Parson
Journal:  Int J Legal Med       Date:  2008-12-17       Impact factor: 2.686

5.  Distinct breakpoints in two cases with deletion in the Yp11.2 region in Japanese population.

Authors:  Reiko Kumagai; Yoshitoshi Sasaki; Takuya Tokuta; Hitoshi Biwasaka; Aya Matsusue; Yasuhiro Aoki; Koji Dewa
Journal:  Hum Genet       Date:  2010-02-03       Impact factor: 4.132

6.  Sex determination.

Authors:  Eleanor A M Graham
Journal:  Forensic Sci Med Pathol       Date:  2006-12       Impact factor: 2.007

7.  A large interstitial deletion encompassing the amelogenin gene on the short arm of the Y chromosome.

Authors:  Wanda Lattanzi; Marilena C Di Giacomo; Gennaro M Lenato; Guglielmina Chimienti; Gianfranco Voglino; Nicoletta Resta; Gabriella Pepe; Ginevra Guanti
Journal:  Hum Genet       Date:  2005-02-22       Impact factor: 4.132

Review 8.  Alternatives to amelogenin markers for sex determination in humans and their forensic relevance.

Authors:  Hirak R Dash; Neha Rawat; Surajit Das
Journal:  Mol Biol Rep       Date:  2020-01-25       Impact factor: 2.316

9.  Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y.

Authors:  Mark A Jobling; Iek Chi C Lo; Daniel J Turner; Georgina R Bowden; Andrew C Lee; Yali Xue; Denise Carvalho-Silva; Matthew E Hurles; Susan M Adams; Yuet Meng Chang; Thirsa Kraaijenbrink; Jürgen Henke; Ginevra Guanti; Brian McKeown; Roland A H van Oorschot; R John Mitchell; Peter de Knijff; Chris Tyler-Smith; Emma J Parkin
Journal:  Hum Mol Genet       Date:  2006-12-22       Impact factor: 6.150

10.  Deletions in the Y-derived amelogenin gene fragment in the Indian population.

Authors:  V K Kashyap; Sanghamitra Sahoo; T Sitalaximi; R Trivedi
Journal:  BMC Med Genet       Date:  2006-04-10       Impact factor: 2.103

  10 in total

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