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PMID: 8513971 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Human skeletal muscle insulin receptor substrate-1. Characterization of the cDNA, gene, and chromosomal localization.

Diabetes ·Vol. 42 ·No. 7 ·1993-07-00 ·Pages 1041-54

Araki E, Sun XJ, Haag BL, Chuang LM, Zhang Y, Yang-Feng TL, White MF, Kahn CR

Abstract

Insulin receptor substrate-1 is a major substrate of insulin receptor Tyr kinase. We have now cloned the IRS-1 cDNA from human skeletal muscle, one of the most important target tissues of insulin action, localized and cloned the human IRS-1 gene, and studied the expression of the protein in Chinese hamster ovary cells. Human IRS-1 cDNA encodes a 1242 amino acid sequence that is 88% identical with rat liver IRS-1. The 14 potential Tyr phosphorylation sites include 6 Tyr-Met-X-Met motifs and 3 Tyr-X-X-Met motifs that are completely conserved in human IRS-1. Human IRS-1 has > 50 possible Ser/Thr phosphorylation sites and one potential ATP-binding site close to the NH2-terminal. The human IRS-1 gene contains the entire 5'-untranslated region and protein coding region in a single exon and was localized on chromosome 2 q36-37 by in situ hybridization. By Northern blot analysis, IRS-1 mRNA is rare and consists of two species of 6.9 and 6 kilobase. By using quantitative polymerase chain reaction after reverse transcription of total RNA from human fetal tissues, IRS-1 mRNA could be identified in all tissues. When human IRS-1 cDNA was expressed in Chinese hamster ovary cells, the protein migrated between 170,000-180,000 M(r) in sodium dodecyl sulfate-polyacrylamide gel electrophoresis and was rapidly Tyr phosphorylated upon insulin stimulation. Thus, IRS-1 is widely expressed and highly conserved across species and tissues.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Amino Acid Sequence Animals Base Sequence CHO Cells Chromosome Mapping Chromosomes, Human, Pair 2 Cloning, Molecular Cricetinae DNA Fetus Gene Expression Genomic Library Humans In Situ Hybridization Insulin Receptor Substrate Proteins Liver/metabolism Molecular Sequence Data Muscles/metabolism Oligodeoxyribonucleotides Phosphoproteins/biosynthesis,genetics Polymerase Chain Reaction RNA, Messenger/biosynthesis,metabolism Rats Sequence Homology, Amino Acid Transcription, Genetic Transfection
Chemicals
IRS1 protein, human Insulin Receptor Substrate Proteins Irs1 protein, rat Oligodeoxyribonucleotides Phosphoproteins RNA, Messenger DNA
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Araki E
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Sun X J
Haag B L
Chuang L M
Zhang Y
Yang-Feng T L
White M F
Kahn C R
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
1993-07-00
Pages
1041-54
Language
English
Region
United States
NLM ID
0372763
Subset
IM
Grants
NIDDK NIH HHS · DK33201 · United States
NIDDK NIH HHS · DK36836 · United States
NIDDK NIH HHS · DK43808 · United States
Databases
GENBANK
D14315, D14316, D14317, D14318, L13313, L13314, L13315, L13316, S62539, X75014
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