Quantification of CFTR transcripts

Methods Mol Biol. 2011:741:115-35. doi: 10.1007/978-1-61779-117-8_9.

Abstract

Quantification and analysis of CFTR transcripts is of crucial importance not only for cystic fibrosis (CF) diagnosis and prognosis, but also in evaluating the efficiency of various therapeutic approaches to CF, including gene therapy. Reverse transcription (RT) followed by quantitative polymerase chain reaction (qPCR) is at present the most sensitive method for transcript abundance measurement. Classical RNA-based methods require significant expression levels in target samples for appropriate analysis, thus PCR-based methods have evolved towards reliable quantification. In this chapter we describe and discuss several protocols for the quantitative analysis of CFTR transcripts, including those variants that result from alternative splicing.

MeSH terms

  • Actins / genetics
  • Alleles
  • Base Sequence
  • Bronchi / cytology
  • Bronchi / pathology
  • Calibration
  • Cell Extracts
  • Cells, Cultured
  • Chemical Fractionation
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / pathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA Primers / genetics
  • DNA, Complementary / genetics
  • Electrophoresis, Agar Gel
  • Genetic Techniques*
  • Humans
  • Nasal Mucosa / cytology
  • Protein Isoforms / genetics
  • Quality Control
  • RNA, Messenger / genetics
  • RNA, Messenger / isolation & purification
  • RNA, Messenger / metabolism
  • Reference Standards
  • Reverse Transcriptase Polymerase Chain Reaction / standards
  • Spectrophotometry
  • Trypsin / metabolism

Substances

  • Actins
  • Cell Extracts
  • DNA Primers
  • DNA, Complementary
  • Protein Isoforms
  • RNA, Messenger
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Trypsin