Araki E, Sun X J, Haag B L, Chuang L M, Zhang Y, Yang-Feng T L, White M F, Kahn C R
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Diabetes. 1993 Jul;42(7):1041-54. doi: 10.2337/diab.42.7.1041.
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)
胰岛素受体底物-1是胰岛素受体酪氨酸激酶的主要底物。我们现已从人类骨骼肌(胰岛素作用最重要的靶组织之一)中克隆出IRS-1 cDNA,定位并克隆了人类IRS-1基因,还研究了该蛋白在中国仓鼠卵巢细胞中的表达情况。人类IRS-1 cDNA编码一个由1242个氨基酸组成的序列,与大鼠肝脏IRS-1的序列有88%的同源性。14个潜在的酪氨酸磷酸化位点包括6个Tyr-Met-X-Met基序和3个Tyr-X-X-Met基序,这些基序在人类IRS-1中完全保守。人类IRS-1有超过50个可能的丝氨酸/苏氨酸磷酸化位点,且在靠近氨基末端处有一个潜在的ATP结合位点。人类IRS-1基因在单个外显子中包含整个5'非翻译区和蛋白质编码区,并通过原位杂交定位在2号染色体q36-37上。通过Northern印迹分析,IRS-1 mRNA含量稀少,由6.9和6千碱基的两种mRNA组成。通过对人类胎儿组织总RNA进行逆转录后使用定量聚合酶链反应,可在所有组织中鉴定出IRS-1 mRNA。当人类IRS-1 cDNA在中国仓鼠卵巢细胞中表达时,该蛋白在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中的迁移分子量在170,000 - 180,000 M(r)之间,并且在胰岛素刺激后迅速发生酪氨酸磷酸化。因此,IRS-1在物种和组织中广泛表达且高度保守。(摘要截短至250字)