Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1987 Nov;84(22):7886-90.
doi: 10.1073/pnas.84.22.7886.

A small multigene family encodes Gi signal-transduction proteins

Affiliations
Comparative Study

A small multigene family encodes Gi signal-transduction proteins

C R Beals et al. Proc Natl Acad Sci U S A. 1987 Nov.

Abstract

The guanine nucleotide-binding regulatory proteins known as G proteins are receptor-associated signal-transduction molecules that are implicated in the control of a variety of metabolic processes. Recent evidence suggests that G proteins may mediate B-lymphocyte responses to bacterial lipopolysaccharide and may also transduce signals from the T-cell antigen receptor. Since these receptors are uniquely expressed on lymphoid cells, we used molecular cloning strategies to ask whether lymphocytes contain specialized G-protein alpha subunits to assist in signal transduction. Comparison of our two deduced human alpha i amino acid sequences with those previously determined for bovine and rodent G proteins permits the identification of three closely related but distinct types of alpha i molecules that comprise a small multigene family. Using gene-specific probes, we found that both of our alpha i genes are expressed in most cell types but in differing ratios. Our data support the view that a modest repertoire of extremely closely related G proteins mediates the transduction of signals derived from multiple different receptor molecules.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Biol Chem. 1986 Jul 25;261(21):9587-90 - PubMed
    1. Proc Natl Acad Sci U S A. 1986 Jun;83(11):3776-80 - PubMed
    1. Proc Natl Acad Sci U S A. 1986 Sep;83(18):6687-91 - PubMed
    1. Science. 1986 Oct 3;234(4772):77-80 - PubMed
    1. Proc Natl Acad Sci U S A. 1986 Oct;83(20):7663-7 - PubMed

Publication types

Associated data

LinkOut - more resources