Early postmortem interval (EPMI) estimation using differentially expressed gene transcripts

Leg Med (Tokyo). 2019 May:38:83-91. doi: 10.1016/j.legalmed.2019.04.008. Epub 2019 May 2.

Abstract

Genes differentially expressed after death were selected to construct a mathematical model for early postmortem interval estimation. Sprague Dawley rats were sacrificed and placed at temperatures of 4 °C, 15 °C, 25 °C, and 35 °C. Brain tissues were collected at 0, 6, 12, 18, and 24 h after death and total RNA was extracted. Changes in gene transcript levels after death were detected using microarray expression profiling and differentially expressed genes was screened. Expanded experiments were performed to validate gene transcript levels at different temperatures using the reverse transcription real-time quantitative polymerase chain reaction. Six genes with high coefficients of determination were chosen for construction of mathematical models. Optimal ternary cubic equations were built using R software with temperature, postmortem interval and ΔCq defined as the independent variable x, y and z, respectively. Equations were converted into a three-dimensional visual statistical model using MATLAB. Animal samples were used to validate the mathematical models. Results showed that the 5srRNA showed best stability at four temperatures. The genes Ninj2, Grifin, Arpp19, and Hopx showed high coefficients of determination (>80%) and low error (<3h) in verification experiments which indicate that they are potential markers for early postmortem interval estimation.

Keywords: Early postmortem interval; Forensic pathology; Gene transcripts; R software; Three-dimensional models.

MeSH terms

  • Animals
  • Biomarkers
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / metabolism
  • Eye Proteins / genetics
  • Eye Proteins / metabolism
  • Forensic Medicine / methods*
  • Galectins / genetics
  • Galectins / metabolism
  • Gene Expression*
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Microarray Analysis
  • Models, Theoretical
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Postmortem Changes*
  • RNA / genetics*
  • RNA / isolation & purification*
  • Rats, Sprague-Dawley
  • Real-Time Polymerase Chain Reaction
  • Temperature
  • Time Factors
  • Transcription, Genetic*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism

Substances

  • Biomarkers
  • Cell Adhesion Molecules, Neuronal
  • Eye Proteins
  • GRIFIN protein, rat
  • Galectins
  • HOPX protein, human
  • Homeodomain Proteins
  • Nerve Growth Factors
  • Ninj1 protein, rat
  • Phosphoproteins
  • Tumor Suppressor Proteins
  • cyclic AMP-regulated phosphoprotein 19
  • RNA