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GTP酶抑制性突变激活人类肿瘤中Gs的α链。

GTPase-inhibiting mutations activate the alpha-chain of Gs in human tumours.

作者信息

Vallar L

机构信息

Department of Pharmacology, C.N.R. Center of Cytopharmacology, Scientific Institute San Raffaele, University of Milan, Italy.

出版信息

Biochem Soc Symp. 1990;56:165-70.

PMID:2124121
Abstract

Several trophic hormones transmit their signals by coupling to G-proteins. A subset of human growth hormone (GH)-secreting pituitary tumours, characterized by elevated GH secretion, cyclic AMP levels, and adenylyl cyclase activity, carries mutations in the gene that encodes the alpha-chain of Gs. By substitution of a single amino acid (Arg-201 or Gln-227), these mutations inhibit the intrinsic GTPase activity of alpha s, thus stabilizing the protein in its active conformation. The discovery of mutant alpha s proteins in human tumours suggests that the alpha s gene can be converted into an oncogene, called gsp, in cells that proliferate in response to cyclic AMP. Most likely, oncogenes can result from similar mutations in other G-protein alpha-chain genes.

摘要

几种促激素通过与G蛋白偶联来传递信号。一部分分泌人生长激素(GH)的垂体肿瘤,其特征是GH分泌增加、环磷酸腺苷(cAMP)水平升高和腺苷酸环化酶活性增强,这些肿瘤在编码Gsα链的基因中存在突变。通过单个氨基酸的替换(Arg-201或Gln-227),这些突变抑制了αs的内在GTP酶活性,从而使该蛋白稳定在其活性构象。在人类肿瘤中发现突变的αs蛋白表明,在响应cAMP而增殖的细胞中,αs基因可以转化为一种癌基因,称为gsp。很可能,癌基因可由其他G蛋白α链基因中的类似突变产生。

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