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Evaluation of skin- or sweat-characteristic mRNAs for inferring the human origin of touched contact traces.
Akutsu, Tomoko; Watanabe, Ken; Takamura, Ayari; Sakurada, Koichi.
Afiliación
  • Akutsu T; National Research Institute of Police Science, Chiba, Japan. Electronic address: tomoko@nrips.go.jp.
  • Watanabe K; National Research Institute of Police Science, Chiba, Japan.
  • Takamura A; National Research Institute of Police Science, Chiba, Japan.
  • Sakurada K; Department of Forensic Dentistry, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Leg Med (Tokyo) ; 33: 36-41, 2018 May 14.
Article en En | MEDLINE | ID: mdl-29777949
ABSTRACT
The source of small amounts of touch DNA, which is transferred from the skin to an object when it is handled or touched, could be an issue in the forensic analysis of criminal cases. Here, we performed an extended evaluation of skin- or sweat-characteristic mRNAs to investigate their usability to infer whether an object has been handled or touched by someone. First, we compared the expression levels of candidate genes between skin swabs and other body fluids by quantitative RT-PCR analysis. Among the analyzed genes, corneodesmosin (CDSN), late cornified envelope 1C (LCE1C), filaggrin (FLG), desmocollin 1, and dermcidin were selected for further analysis on the basis of their specificities and sensitivities. Then, we tried to detect these genes from mock casework samples. As a result, CDSN, LCE1C, and FLG could be good markers because of their detectability. Finally, we determined the correlation between the expression of these genes and DNA yield of skin swabs to assess their adaptability as a screening test for touch DNA samples. However, the detectability of these genes was not correlated with the DNA yield of skin swab samples. In conclusion, gene expression analysis of the skin- or sweat-characteristic mRNAs CDSN, LCE1C, and FLG could be useful for inferring the skin origin of touched contact traces, but the use of the expression levels of these mRNAs for the prediction of DNA yield is problematic. To develop a screening test for touch DNA samples, other markers that have a well-correlated sensitivity with DNA analysis should be investigated.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Leg Med (Tokyo) Asunto de la revista: JURISPRUDENCIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Leg Med (Tokyo) Asunto de la revista: JURISPRUDENCIA Año: 2018 Tipo del documento: Article