Forensic Science International: Genetics
Volume 3, Issue 2 , Pages 74-79, March 2009

Novel methods of molecular sex identification from skeletal tissue using the amelogenin gene

  • Victoria Gibbon

      Affiliations

    • Department of Internal Medicine, University of the Witwatersrand, 7 York Rd, Johannesburg, 2193 Parktown, South Africa
    • School of Geography, Archaeology and Environmental Studies, University of the Witwatersrand, 7 York Rd, Johannesburg, 2193 Parktown, South Africa
    • Corresponding Author InformationCorresponding author at: School of Geography, Archaeology and Environmental Studies, University of the Witwatersrand, 7 York Rd, Johannesburg, 2193 Parktown, South Africa. Tel.: +27 11 488 3632.
  • ,
  • Maria Paximadis

      Affiliations

    • AIDS Virus Research Unit, National Institute of Communicable Diseases, Sandringham, Johannesburg, South Africa
  • ,
  • Goran Štrkalj

      Affiliations

    • Department of Health and Chiropractic, Macquarie University, Sydney, NSW 2109, Australia
  • ,
  • Paul Ruff

      Affiliations

    • Department of Internal Medicine, University of the Witwatersrand, 7 York Rd, Johannesburg, 2193 Parktown, South Africa
  • ,
  • Clem Penny

      Affiliations

    • Department of Internal Medicine, University of the Witwatersrand, 7 York Rd, Johannesburg, 2193 Parktown, South Africa

Received 3 July 2008; received in revised form 22 September 2008; accepted 15 October 2008. published online 15 December 2008.

Abstract 

Sex identification from skeletal material is of vital importance in order to reconstruct the demographic variables of an individual in forensic genetics and ancient DNA (aDNA) analysis. When the use of conventional methods of sex identification are impossible, molecular analysis of the X and Y chromosomes provides an expedient solution. Two novel systems of molecular sex identification suitable for skeletal material using the amelogenin gene are described, beginning in intron 2–3, spanning exon 3 and ending in intron 3–4. This area was optimal for sexing, as it includes 14 sex-specific polymorphic regions in addition to an indel (insertion or deletion of nucleotides). Once optimised and working with 100% efficiency on the controls, these procedures were applied to a collection of miscellaneous archaeological skeletons (ex situ) sourced from the Raymond Dart Collection of Human Skeletons (Dart Collection). This collection was used to optimise these techniques for skeletal remains derived from an archaeological context. These methods produced 46.66% sex results for the ex situ sample, which is within the normal range for aDNA studies. These new techniques are optimal for sex identification, with both the inherent control of isolating many sex-specific features and combined with the use of sensitive micro-fluidic electrophoresis.

Keywords: Skeletal remains, Ancient DNA, Sex identification, Amelogenin gene

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PII: S1872-4973(08)00147-6

doi:10.1016/j.fsigen.2008.10.007

Forensic Science International: Genetics
Volume 3, Issue 2 , Pages 74-79, March 2009