Sun X J, Pons S, Wang L M, Zhang Y, Yenush L, Burks D, Myers M G, Glasheen E, Copeland N G, Jenkins N A, Pierce J H, White M F
Department of Medicine, Harvard Medical School, Boston, Massachusetts 02215, USA.
Mol Endocrinol. 1997 Feb;11(2):251-62. doi: 10.1210/mend.11.2.9885.
Signal transduction by insulin and IGF-1, several interleukins (IL-2, IL-4, IL-9, IL-13), interferons, GH, and other cytokines involves IRS proteins, which link the receptors for these factors to signaling molecules with Src homology-2 domains (SH2-proteins). We recently reported the amino acid sequence of murine IRS-2; in order to examine a potential genetic role for this molecule in disease, we isolated the murine IRS-2 gene and compared the expression pattern of IRS-2 against IRS-1. Like IRS-1, IRS-2 is encoded by a single exon. Whereas IRS-1 is located on murine chromosome 1, IRS-2 is located on murine chromosome 8 near the insulin receptor. IRS-2 is expressed together with IRS-1 in many cells and tissues; however, IRS-2 predominates in murine hematopoietic cells where it may be essential for cytokine signaling; IRS-1 predominates in adipocytes and differentiated 3T3-L1 cells where it contributes to the normal insulin response. In 32D cells, IRS-1 and IRS-2 undergo differential tyrosine phosphorylation during insulin or IL-4 stimulation, as assessed indirectly by interaction with various recombinant SH2 domains. Thus, signaling specificity through the IRS proteins may be accomplished by specific expression patterns and distinct phosphorylation patterns during interaction with various activated receptors.
胰岛素、胰岛素样生长因子-1、多种白细胞介素(白细胞介素-2、白细胞介素-4、白细胞介素-9、白细胞介素-13)、干扰素、生长激素及其他细胞因子的信号转导涉及胰岛素受体底物(IRS)蛋白,这些蛋白将这些因子的受体与具有Src同源结构域2的信号分子(SH2蛋白)相连。我们最近报道了小鼠IRS-2的氨基酸序列;为了研究该分子在疾病中的潜在遗传作用,我们分离了小鼠IRS-2基因,并比较了IRS-2与IRS-1的表达模式。与IRS-1一样,IRS-2由单个外显子编码。IRS-1位于小鼠1号染色体上,而IRS-2位于小鼠8号染色体上靠近胰岛素受体的位置。IRS-2与IRS-1在许多细胞和组织中共同表达;然而,IRS-2在小鼠造血细胞中占主导地位,在其中它可能对细胞因子信号传导至关重要;IRS-1在脂肪细胞和分化的3T3-L1细胞中占主导地位,在其中它有助于正常的胰岛素反应。在32D细胞中,在胰岛素或白细胞介素-4刺激期间,IRS-1和IRS-2经历不同的酪氨酸磷酸化,这通过与各种重组SH2结构域的相互作用间接评估。因此,通过IRS蛋白的信号特异性可能通过与各种活化受体相互作用期间的特定表达模式和不同的磷酸化模式来实现。