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Human skeletal muscle insulin receptor substrate-1. Characterization of the cDNA, gene, and chromosomal localization.
Araki, E; Sun, X J; Haag, B L; Chuang, L M; Zhang, Y; Yang-Feng, T L; White, M F; Kahn, C R.
Afiliación
  • Araki E; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Diabetes ; 42(7): 1041-54, 1993 Jul.
Article en En | MEDLINE | ID: mdl-8513971
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)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Cromosomas Humanos Par 2 / ADN / Expresión Génica / Músculos Límite: Animals / Humans Idioma: En Revista: Diabetes Año: 1993 Tipo del documento: Article
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Cromosomas Humanos Par 2 / ADN / Expresión Génica / Músculos Límite: Animals / Humans Idioma: En Revista: Diabetes Año: 1993 Tipo del documento: Article