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人及小鼠G蛋白信号调节剂GAIP/RGS19的基因结构、双启动子及mRNA可变剪接

Gene structure, dual-promoters and mRNA alternative splicing of the human and mouse regulator of G protein signaling GAIP/RGS19.

作者信息

Xie Guo-xi, Han Xiaokang, Ito Emi, Yanagisawa Yuka, Maruyama Kazuo, Sugano Sumio, Suzuki Yutaka, Wang Yan, Gabriel Anja, Stevens Sarah K, Mitchell James, Sharma Manohar, Palmer Pamela Pierce

机构信息

Department of Anesthesia and Perioperative Medicine, University of California, 513 Parnassus Avenue, San Francisco, CA 94143-0464, USA.

出版信息

J Mol Biol. 2003 Jan 24;325(4):721-32. doi: 10.1016/s0022-2836(02)01283-4.

Abstract

Here we report the gene structure and transcription regulation of the human and mouse G protein-signaling regulator GAIP/RGS19. The GAIP/RGS19 gene is adjacent to and in an opposite orientation to the opioid-receptor-like receptor 1 (ORL1) gene. In both human and mouse, the GAIP/RGS19 gene is composed of seven exons. The first two exons are under the control of two different promoters and are alternatively employed to start the transcription of two 5' distinctive mRNAs. The two promoters appear to compete with and inhibit each other. We have also identified in mice an alternatively spliced short GAIP/RGS19 mRNA that lacks the exon 2 region and utilizes an ATG in exon 3 as its translation initiation codon. As a result, the short GAIP/RGS19 protein does not have the N-terminal 22 amino acid residues of a full-length isoform. GAIP/RGS19 alternative splicing patterns are differentially expressed in various tissues. The mRNA alternative splicing to produce multiple isoforms may play a significant role in regulating the function and selectivity of GAIP/RGS19.

摘要

在此,我们报告人类和小鼠G蛋白信号调节剂GAIP/RGS19的基因结构及转录调控。GAIP/RGS19基因与阿片样受体样受体1(ORL1)基因相邻且方向相反。在人类和小鼠中,GAIP/RGS19基因均由七个外显子组成。前两个外显子受两个不同启动子的控制,并交替用于启动两种5'端不同的mRNA的转录。这两个启动子似乎相互竞争并相互抑制。我们还在小鼠中鉴定出一种选择性剪接的短GAIP/RGS19 mRNA,其缺少外显子2区域,并利用外显子3中的一个ATG作为其翻译起始密码子。因此,短GAIP/RGS19蛋白不具有全长异构体的N端22个氨基酸残基。GAIP/RGS19的选择性剪接模式在各种组织中差异表达。mRNA的选择性剪接产生多种异构体可能在调节GAIP/RGS19的功能和选择性方面发挥重要作用。

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