Reverse transcriptase-polymerase chain reaction assay for acetylcholinesterase mRNA in rat brain

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

In order to examine the molecular basis for regional variation in expression of brain acetylcholinesterase (AChE), an assay using reverse transcription and polymerase chain reaction (RT-PCR) was developed to measure steady state levels of AChE mRNA. The amplification method was designed to be specific for templates derived from AChE mRNA and to avoid potential artifacts induced by the presence of genomic DNA. RT-PCR made it possible to assay AChE mRNA in milligram samples from different regions of the rat brain. Determinations by RT-PCR were faster and more sensitive than Northern blotting. The results, including a surprisingly low level of AChE mRNA in the caudate nucleus, agreed with earlier observations by Northern blot and in- situ hybridization. Quantitative RT-PCR may be useful in future studies on developmental and physiological regulation of AChE expression in the brain.

Original languageEnglish (US)
Pages (from-to)129-135
Number of pages7
JournalNeurochemical Research
Volume20
Issue number2
DOIs
StatePublished - 1995

Fingerprint

Polymerase chain reaction
RNA-Directed DNA Polymerase
Acetylcholinesterase
Reverse Transcriptase Polymerase Chain Reaction
Rats
Assays
Brain
Transcription
Messenger RNA
Reverse Transcription
Polymerase Chain Reaction
Northern Blotting
Caudate Nucleus
Artifacts
In Situ Hybridization
Amplification
DNA

Keywords

  • cholinesterase expression
  • Neurochemical methods
  • regional brain dissection

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry

Cite this

Reverse transcriptase-polymerase chain reaction assay for acetylcholinesterase mRNA in rat brain. / Rao, R.; Brimijoin, William Stephen.

In: Neurochemical Research, Vol. 20, No. 2, 1995, p. 129-135.

Research output: Contribution to journalArticle

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