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人类生长因子结合蛋白GRB2的基因结构。

The gene structure of the human growth factor bound protein GRB2.

作者信息

Bochmann H, Gehrisch S, Jaross W

机构信息

Institut für Klinische Chemie und Laboratoriumsmedizin, Universitätsklinikum der Technischen Universität Dresden, Dresden, 01307,

出版信息

Genomics. 1999 Mar 1;56(2):203-7. doi: 10.1006/geno.1998.5692.

Abstract

The growth factor bound protein GRB2, a 25-kDa cytosolic protein, plays a key role in two separate pathways of the insulin signal transduction system leading from the insulin receptor to the Ras proteins and thus affecting mitogenic signaling. GRB2 regulates Ras activation through association with the guanine nucleotide exchange factor Sos. The GRB2/Sos complex can connect with insulin receptor substrate 1 (IRS-1), which is one of the primary targets of the insulin and insulin-like growth factor receptors. In a second pathway, independent of IRS-1, GRB2 links the insulin receptor to Ras signaling through another adapter protein, called Shc. In protooncogenic and other noninsulin signaling systems, GRB2 appears to link receptor tyrosine kinases to Ras in similar pathways as well. This study presents the exon-intron organization of the human GRB2 gene. After primers were placed across the known mRNA sequence, Long PCR products spanning introns and their adjacent splice sites were amplified and adequately sequenced to establish the splice sites and flanking regions. The gene was found to consist of five exons (ranging from 78 to 186 bp) and of four introns (from approximately 1 to approximately 7 kb). Intron primers for the respective exons were generated using the newly found flanking sequences. All exons were successfully amplified and sequenced, and the data obtained from Long PCR sequencing were confirmed.

摘要

生长因子结合蛋白GRB2是一种25kDa的胞质蛋白,在胰岛素信号转导系统从胰岛素受体到Ras蛋白的两条独立途径中起关键作用,从而影响有丝分裂信号传导。GRB2通过与鸟嘌呤核苷酸交换因子Sos结合来调节Ras激活。GRB2/Sos复合物可与胰岛素受体底物1(IRS-1)相连,IRS-1是胰岛素和胰岛素样生长因子受体的主要靶点之一。在第二条独立于IRS-1的途径中,GRB2通过另一种称为Shc的衔接蛋白将胰岛素受体与Ras信号传导联系起来。在原癌基因和其他非胰岛素信号系统中,GRB2似乎也在类似途径中将受体酪氨酸激酶与Ras联系起来。本研究展示了人类GRB2基因的外显子-内含子结构。在引物跨越已知mRNA序列放置后,扩增出跨越内含子及其相邻剪接位点的长PCR产物并进行充分测序,以确定剪接位点和侧翼区域。发现该基因由五个外显子(78至186bp)和四个内含子(约1至约7kb)组成。利用新发现的侧翼序列生成了各个外显子的内含子引物。所有外显子均成功扩增并测序,长PCR测序获得的数据得到了证实。

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