GNAZ in human fetal cochlea: expression, localization, and potential role in inner ear function

I Magovcevic, U Khetarpal, F R Bieber, C C Morton

Research output: Contribution to journalArticlepeer-review

Abstract

Dissociation of an activated alpha-subunit from the beta-gamma complex directly regulates secondary messenger proteins. To address the potential role of G proteins expressed in human fetal cochlea, degenerate oligonucleotide primers corresponding to the 3'-end of the conserved region of alpha-subunits were used for polymerase chain reaction amplification of reverse-transcribed total human fetal cochlear mRNAs; GNAZ and GNAQ were isolated. These two G proteins are unique among the G-protein family because they lack a typical pertussis modification site. GNAZ is expressed in high levels in neural tissue while GNAQ is ubiquitously expressed. We characterized GNAZ expression using Northern blots, tissue in-situ hybridization and immunohistochemistry techniques to elucidate the potential role of this protein in inner ear function. Our data suggest that GNAZ may play a role in maintaining the ionic balance of perilymphatic and endolymphatic cochlear fluids.

Original languageEnglish
Pages (from-to)55-64
Number of pages10
JournalHearing Research
Volume90
Issue number1-2
Publication statusPublished - Oct 1995

Keywords

  • Autoradiography
  • Base Sequence
  • Blotting, Northern
  • Cloning, Molecular
  • Cochlea
  • DNA
  • Ear, Inner
  • Fetal Proteins
  • GTP-Binding Proteins
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Molecular Sequence Data
  • Perilymph
  • Polymerase Chain Reaction
  • RNA, Messenger
  • Second Messenger Systems
  • Transcription, Genetic
  • Journal Article
  • Research Support, U.S. Gov't, P.H.S.

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