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October 1, 1987Journal of Biological Chemistry759 citationsOpen Access

Molecular cloning of five GTP-binding protein cDNA species from rat olfactory neuroepithelium.

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DJDavid T. JonesRRRandall R. Reed

Key Points

  • To identify the specific GTP-binding protein (G-protein) alpha subunits responsible for mediating olfactory signal transduction in vertebrate neuroepithelium.
  • Screened a rat olfactory cDNA library using oligonucleotide probes.
  • Isolated recombinant clones to characterize distinct G-protein alpha subunits and analyzed tissue-specific mRNA expression profiles.
  • Isolated 32 recombinant clones encoding five distinct G-protein alpha subunit types: G alpha s, G alpha o, G alpha i1, G alpha i2, and a novel species, G alpha i3.
  • Identified G alpha s as the predominant clone and most abundant G-protein alpha subunit transcript in rat olfactory tissue.

Abstract

Biochemical studies in vertebrate olfactory tissue indicate that certain odorants stimulate adenylyl cyclase in a GTP-dependent manner. Additionally, immunochemical and toxin-labeling studies demonstrate the presence of several GTP-binding protein (G-protein) species in vertebrate olfactory epithelium. To identify the G-protein(s) responsible for olfactory signal transduction, we screened a rat olfactory cDNA library with an oligonucleotide probe and isolated 32 recombinant clones encoding five distinct types of G-protein alpha subunits. The majority of the clones encoded G alpha s, while the remaining clones encoded G alpha o, G alpha i1, G alpha i2, and a novel species, G alpha i3. Messenger RNA corresponding to each G alpha was detectable in all tissues examined; however, the levels for a given G alpha varied in a tissue-specific manner. In olfactory tissue, G alpha s was the most abundant of these messages and in combination with the biochemical studies suggests that G alpha s is the G-protein component of the olfactory signal transduction cascade.

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Cite This Study

Jones et al. (1987) studied this question.

synapsesocial.com/papers/6a0975d087ad1657d2515768https://doi.org/10.1016/s0021-9258(18)47929-x
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