Forensic Science International: Genetics
Volume 6, Issue 4 , Pages 452-460, July 2012

Evaluation of mRNA marker specificity for the identification of five human body fluids by capillary electrophoresis

  • Mara L. Lennard Richard

      Affiliations

    • Counterterrorism and Forensic Science Research Unit, FBI Laboratory Division, 2501 Investigation Parkway, Quantico, VA 22135, United States
  • ,
  • Kathryn A. Harper

      Affiliations

    • Counterterrorism and Forensic Science Research Unit, FBI Laboratory Division, 2501 Investigation Parkway, Quantico, VA 22135, United States
  • ,
  • Rhonda L. Craig

      Affiliations

    • Nuclear DNA Unit, FBI Laboratory Division, Quantico, VA 22135, United States
  • ,
  • Anthony J. Onorato

      Affiliations

    • Nuclear DNA Unit, FBI Laboratory Division, Quantico, VA 22135, United States
  • ,
  • James M. Robertson

      Affiliations

    • Counterterrorism and Forensic Science Research Unit, FBI Laboratory Division, 2501 Investigation Parkway, Quantico, VA 22135, United States
  • ,
  • Joseph Donfack

      Affiliations

    • Counterterrorism and Forensic Science Research Unit, FBI Laboratory Division, 2501 Investigation Parkway, Quantico, VA 22135, United States
    • Corresponding Author InformationCorresponding author. Tel.: +1 703 632 4593; fax: +1 703 632 7801.

Received 18 February 2011; received in revised form 22 September 2011; accepted 24 September 2011. published online 17 October 2011.

Abstract 

The identification of forensically relevant human body fluids through messenger RNA (mRNA) profiling is of interest to the forensic community. Previous studies have proposed several tissue-specific mRNA markers to achieve this goal. Seven markers for the following genes were selected for evaluation in this study: histatin 3 (HTN3) and statherin (STATH) for saliva, mucin 4 (MUC4) for vaginal secretions, matrix metalloproteinase 7 (MMP7) for menstrual blood, delta-aminolevulinate synthase 2 (ALAS2) for peripheral blood, and protamine 2 (PRM2) and transglutaminase 4 (TGM4) for semen. The expression of these markers was examined in each body fluid. All mRNA markers were present in their target body fluids. Peripheral blood and saliva showed little cross-reactivity with the selected markers. However, a high level of cross-reactivity was observed between the vaginal secretion marker MUC4 and saliva stains. Semen showed a high level of cross-reactivity with the selected markers. Co-expression of the predicted body fluid markers was detected in menstrual blood and vaginal secretion stains. The expression pattern of these mRNA markers varied through the menstrual cycle time points tested. Differences in gene expression levels and marker cross-reactivity were observed in the donors tested. Despite the presence of cross-reactivity and co-expression, each of the body fluids examined have distinct gene expression profiles, allowing for body fluid identification based on mRNA profiling.

Keywords: Messenger RNA (mRNA), mRNA profiling, Body fluid identification, Forensic science

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PII: S1872-4973(11)00190-6

doi:10.1016/j.fsigen.2011.09.007

Forensic Science International: Genetics
Volume 6, Issue 4 , Pages 452-460, July 2012