Alternative splicing, gene localization, and binding of SH2-B to the insulin receptor kinase domain

被引:70
作者
Nelms, K
O'Neill, TJ
Li, SQ
Hubbard, SR
Gustafson, TA
Paul, WE
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
[3] NYU, Med Ctr, Skirball Inst Biomol Med, New York, NY 10016 USA
[4] NYU, Med Ctr, Dept Pharmacol, New York, NY 10016 USA
[5] Metabolex Inc, Hayward, CA 94545 USA
关键词
D O I
10.1007/s003359901183
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The SH2-B protein is an SH2-domain-containing molecule that interacts with a number of phosphorylated kinase and receptor molecules including the insulin receptor. Two isoforms of the SH2-B have been identified and have been proposed to arise through alternate splicing. Here we have identified a third isoform of the SH2-B protein, SH2-B gamma, that interacts specifically with the insulin receptor. This interaction required phosphorylation of residue Y1146 in the triple tyrosine motif within the activation loop of the IR kinase and is one of only two signaling molecules shown to interact directly with this residue of the insulin receptor kinase domain. The intron/exon structure of the SH2-B gene was determined. Alternate splice sites utilized to generate the different isoforms of the SH2-B protein were identified in the 3' end of the SH2-B gene immediately downstream of the exon encoding the core of the SH2 domain. Additionally, the chromosomal location of the SH2-B gene was determined to be the distal arm of mouse Chromosome (Chr) 7 in a region linked to obesity in mice.
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页码:1160 / 1167
页数:8
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