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 language | English |
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Pages (from-to) | 55-64 |
Number of pages | 10 |
Journal | Hearing Research |
Volume | 90 |
Issue number | 1-2 |
Publication status | Published - 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.