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一种针对小GTP结合蛋白的刺激性GDP/GTP交换蛋白的转化活性及c-fos启动子/增强子刺激活性。

Transforming and c-fos promoter/enhancer-stimulating activities of a stimulatory GDP/GTP exchange protein for small GTP-binding proteins.

作者信息

Fujioka H, Kaibuchi K, Kishi K, Yamamoto T, Kawamura M, Sakoda T, Mizuno T, Takai Y

机构信息

Department of Biochemistry, Kobe University School of Medicine, Japan.

出版信息

J Biol Chem. 1992 Jan 15;267(2):926-30.

PMID:1730682
Abstract

smg GDP dissociation stimulator (GDS) is a stimulatory GDP/GTP exchange protein for a group of ras p21-like small GTP-binding proteins (G proteins) including c-Ki-ras p21, smg p21A, smg p21B, and rhoA p21. smg GDS converts the GDP-bound inactive form to the GTP-bound active form of each small G protein by stimulating their GDP/GTP exchange reaction in a cell-free system. The point-mutated c-Ki-ras p21 (c-Ki-rasval12 p21) is known to strongly transform NIH/3T3 cells and to markedly stimulate the c-fos promoter/enhancer in this cell line, whereas the normal c-Ki-ras p21 is weak in these activities. In the present study, we examined the effect of smg GDS on these activities to explore its physiological function. Overexpression of both smg GDS and c-Ki-ras p21 strongly transformed NIH/3T3 cells, whereas overexpression of either smg GDS or c-Ki-ras p21 alone weakly transformed the cells. Furthermore, overexpression of both smg GDS and c-Ki-ras p21 markedly stimulated the c-fos promoter/enhancer in NIH/3T3 cells, whereas overexpression of either smg GDS or c-Ki-ras p21 alone weakly stimulated it. These results indicate that smg GDS transforms NIH/3T3 cells and stimulates the c-fos promoter/enhancer in this cell line in cooperation with c-Ki-ras p21.

摘要

小分子量GTP酶GDP解离刺激因子(GDS)是一种对一组ras p21样小GTP结合蛋白(G蛋白)具有刺激作用的GDP/GTP交换蛋白,这些G蛋白包括c-Ki-ras p21、小分子量GTP酶GDS p21A、小分子量GTP酶GDS p21B和rhoA p21。在无细胞系统中,小分子量GTP酶GDS通过刺激其GDP/GTP交换反应,将每个小G蛋白的GDP结合非活性形式转化为GTP结合活性形式。已知点突变的c-Ki-ras p21(c-Ki-rasval12 p21)能强烈转化NIH/3T3细胞,并显著刺激该细胞系中的c-fos启动子/增强子,而正常的c-Ki-ras p21在这些活性方面较弱。在本研究中,我们检测了小分子量GTP酶GDS对这些活性的影响,以探索其生理功能。小分子量GTP酶GDS和c-Ki-ras p21的过表达均能强烈转化NIH/3T3细胞,而单独过表达小分子量GTP酶GDS或c-Ki-ras p21只能微弱地转化细胞。此外,小分子量GTP酶GDS和c-Ki-ras p21的过表达均能显著刺激NIH/3T3细胞中的c-fos启动子/增强子,而单独过表达小分子量GTP酶GDS或c-Ki-ras p21只能微弱地刺激它。这些结果表明,小分子量GTP酶GDS与c-Ki-ras p21协同作用,可转化NIH/3T3细胞并刺激该细胞系中的c-fos启动子/增强子。

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