Stability of RNA transcripts in post-mortem psychiatric brains

J Neural Transm (Vienna). 1999;106(3-4):329-35. doi: 10.1007/s007020050162.

Abstract

RNA isolated from frozen human post-mortem brain tissue was used for analysis of five gene products with a recently developed sensitive and competitive RT-PCR technique. Samples varying in post-mortem intervals up to four days from controls, schizophrenics and alcoholics were analyzed. Evaluation of three housekeeping genes, as well as Trk B and Trk C demonstrated that the levels of mRNA transcripts were stable in brain samples at all time periods (one to four days) examined. This observation demonstrates that this RT-PCR protocol is a sensitive and reliable method to study relative amounts of mRNAs. The overall stability of housekeeping transcripts implicates the value of post-mortem brain samples for differential gene expression studies.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • Adult
  • Aged
  • Alcoholism / metabolism
  • Brain / metabolism*
  • Cadaver
  • Drug Stability
  • Female
  • Glyceraldehyde-3-Phosphate Dehydrogenases / genetics
  • Humans
  • Male
  • Middle Aged
  • RNA, Messenger / chemistry
  • RNA, Messenger / metabolism*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor, Ciliary Neurotrophic Factor
  • Receptor, trkC
  • Receptors, Nerve Growth Factor / genetics
  • Reference Values
  • Reverse Transcriptase Polymerase Chain Reaction
  • Schizophrenia / metabolism*
  • beta 2-Microglobulin / genetics

Substances

  • Actins
  • RNA, Messenger
  • Receptor, Ciliary Neurotrophic Factor
  • Receptors, Nerve Growth Factor
  • beta 2-Microglobulin
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Receptor Protein-Tyrosine Kinases
  • Receptor, trkC