Forensic Science International
Volume 203, Issue 1 , Pages 71-75, 15 December 2010

mRNA profiling in forensic genetics I: Possibilities and limitations

  • Marielle Vennemann

      Affiliations

    • Institute of Legal Medicine, University of Freiburg, Albertstr. 9, 79104 Freiburg, Germany
    • Centre for Forensic Science, Strathclyde University, Royal College, 204 George Stree, Glasgow G1 1XW, Scotland, UK
    • Corresponding Author InformationCorresponding author.
  • ,
  • Antje Koppelkamm

      Affiliations

    • Institute of Legal Medicine, University of Freiburg, Albertstr. 9, 79104 Freiburg, Germany

published online 20 August 2010.

Abstract 

Molecular investigations gain increasing interest in forensic medicine. Examination of gene expression levels at the time point of death might have the power to become a complementing tool to the current methods for the determination of cause and circumstances of death. This includes pathophysiological conditions of disease and injury as well as the duration of agony or other premortem factors. Additionally, recent developments in forensic genetics revealed that tissue specific mRNAs can be used to determine the type of body fluid present in a crime scene stain.

Although RNA is known to be rather instable, RNA could be extracted in adequate quality from tissue samples collected during medico-legal autopsy. Nevertheless, working with human postmortem tissue means to deal with highly variable RNA integrities. This review aims to give a brief overview of the possible advantages of postmortem mRNA profiling and to shed further light into the limitations of this method arising from reduced RNA integrities.

Keywords: mRNA profiling, Post mortem tissue, Degradation, Body fluid identification, Cause of death

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 This paper is part of the special issue entitled: Molecular Pathology in Forensic Medicine, Guest-edited by Burkhard Madea and Pekka Saukko.

PII: S0379-0738(10)00335-X

doi:10.1016/j.forsciint.2010.07.006

Forensic Science International
Volume 203, Issue 1 , Pages 71-75, 15 December 2010