Gridley Scott, Chavez Jose A, Lane William S, Lienhard Gustav E
Department of Biochemistry, Vail Building, Dartmouth Medical School, Hanover, NH 03755, USA.
Cell Signal. 2006 Oct;18(10):1626-32. doi: 10.1016/j.cellsig.2006.01.002. Epub 2006 Feb 21.
Recently we identified a novel 250 kDa protein in adipocytes that is a substrate for the insulin-activated protein kinase Akt. We refer to this protein as AS250 for Akt substrate of 250 kDa. AS250 has a predicted GTPase activating protein (GAP) domain at its carboxy terminus. This domain shows some homology to the GAP domains for Rheb at the carboxy terminus of the protein tuberin and for Rap1 in the protein Rap1 GAP. The present study further characterizes AS250. The cDNA sequence for human AS250 is reported, and the sites that undergo phosphorylation upon insulin treatment of adipocytes have been identified by tandem mass spectrometry. We have found that in adipocytes AS250 exists as a complex with a novel protein of 1484 amino acids known as KIAA1219. The complex of AS250 with KIAA1219 is notably similar to the important regulatory complex of the protein tuberin with hamartin (the tuberous sclerosis complex), in the size of its subunits, the location of the GAP domain, and its phosphorylation by Akt. In an effort to detect the cellular role of the AS250/KIAA1219 complex, we generated 3T3-L1 adipocytes that largely lack AS250 by shRNA knockdown and examined several insulin-dependent effects. The knockdown of AS250 had no effect on insulin activation of the kinases, Akt, 70 kDa S6 kinase, or ERK1/2, or on insulin-stimulated actin bundling, and it had only a slight effect on insulin-stimulated GLUT4 translocation.
最近,我们在脂肪细胞中鉴定出一种新的250 kDa蛋白质,它是胰岛素激活的蛋白激酶Akt的底物。我们将这种蛋白质称为AS250,即250 kDa的Akt底物。AS250在其羧基末端有一个预测的GTP酶激活蛋白(GAP)结构域。该结构域与蛋白质结节性硬化蛋白羧基末端的Rheb的GAP结构域以及蛋白质Rap1 GAP中的Rap1的GAP结构域有一些同源性。本研究进一步对AS250进行了表征。报告了人类AS250的cDNA序列,并通过串联质谱法确定了脂肪细胞经胰岛素处理后发生磷酸化的位点。我们发现,在脂肪细胞中,AS250与一种名为KIAA1219的1484个氨基酸的新蛋白质形成复合物存在。AS250与KIAA1219的复合物在亚基大小、GAP结构域的位置以及被Akt磷酸化方面,与结节性硬化蛋白与错构瘤蛋白(结节性硬化复合物)的重要调节复合物显著相似。为了检测AS250/KIAA1219复合物的细胞作用,我们通过shRNA敲低产生了大量缺乏AS250的3T3-L1脂肪细胞,并检测了几种胰岛素依赖性效应。敲低AS250对激酶Akt、70 kDa S6激酶或ERK1/2的胰岛素激活没有影响,对胰岛素刺激的肌动蛋白束集也没有影响,对胰岛素刺激的GLUT4转位只有轻微影响。