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PMID: 3554510 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Ras p21 as a potential mediator of insulin action in Xenopus oocytes.

Science (New York, N.Y.) ·Vol. 236 ·No. 4803 ·1987-05-15 ·Pages 840-3

Korn LJ, Siebel CW, McCormick F, Roth RA

Abstract

The oncogene protein product (p21) of the ras gene has been implicated in mediating the effects of a variety of growth factors and hormones. Microinjection of monoclonal antibody 6B7, which is directed against a synthetic peptide corresponding to a highly conserved region of p21 (amino acids 29 to 44) required for p21 function, specifically inhibited Xenopus oocyte maturation induced by incubation with insulin. The inhibition was dose-dependent and specific since (i) the same antibody had no effect on progesterone-induced maturation, (ii) immunoprecipitation and Western blotting indicated that the antibody recognized a single protein of molecular weight 21,000 in oocyte extracts, and (iii) inhibition was not observed with identical concentrations of normal immunoglobulin. Thus, p21 appears to be involved in mediating insulin-induced maturation of Xenopus oocytes. Furthermore, the mechanism may involve phosphorylation of p21, as p21 was found to be a substrate of the insulin receptor kinase.

MeSH Terms
Animals Antibodies Female Immunoglobulin G Insulin/pharmacology Oncogenes Oocytes/cytology,drug effects Progesterone/pharmacology Proto-Oncogene Proteins/genetics,physiology Xenopus laevis
Chemicals
Antibodies Immunoglobulin G Insulin Proto-Oncogene Proteins Progesterone
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Korn L J
Siebel C W
McCormick F
Roth R A
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1987-05-15
Pages
840-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIAID NIH HHS · AI 21298 · United States
NIADDK NIH HHS · AM 01393 · United States
NIADDK NIH HHS · AM 34926 · United States
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