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v-mos和c-Ha-ras癌蛋白对蛋白质合成模式产生相似的影响。

The v-mos and c-Ha-ras oncoproteins exert similar effects on the pattern of protein synthesis.

作者信息

Klemenz R, Hoffmann S, Jaggi R, Werenskiold A K

机构信息

Ludwig Institute for Cancer Research, Inselspital, Bern, Switzerland.

出版信息

Oncogene. 1989 Jun;4(6):799-803.

PMID:2525241
Abstract

The effects of the ras and the mos oncogene products on the pattern of newly synthesized proteins was investigated in NIH3T3 cell lines. A conditional expression system which allowed hormonal induction of the oncogenes was utilized to detect effects on the accumulation of oncoproteins by two dimensional gel electrophoresis of crude cell extracts. Strong and reproducible changes of protein synthesis following the expression of the ras and mos oncogenes were detected. Transiently induced synthesis of four proteins with a molecular mass of 23 kDa, 32 kDa, 35 kDa, and 47 kDa was observed. These changes were qualitatively indistinguishable in both, ras and mos oncogene expressing cells. This is in agreement with the notion that the two oncogene products act on a common signal transduction pathway. Serum mediated growth induction of quiescent NIH3T3 cells led to a different pattern of altered protein synthesis. We observed the transient alteration in the synthesis rates of three proteins with a molecular mass of 27 kDa, 47 kDa and 52 kDa. Only the 47 kDa protein was also subject to regulation by the oncoproteins. One of the proteins whose synthesis was strongly induced by the ras and mos oncogene products is also expressed by heat shock.

摘要

在NIH3T3细胞系中研究了ras和mos癌基因产物对新合成蛋白质模式的影响。利用一种条件表达系统,该系统允许通过激素诱导癌基因,通过对粗细胞提取物进行二维凝胶电泳来检测对癌蛋白积累的影响。在ras和mos癌基因表达后,检测到蛋白质合成发生了强烈且可重复的变化。观察到瞬时诱导合成了四种分子量分别为23 kDa、32 kDa、35 kDa和47 kDa的蛋白质。在表达ras和mos癌基因的细胞中,这些变化在质量上无法区分。这与两种癌基因产物作用于共同信号转导途径的观点一致。血清介导的静止NIH3T3细胞的生长诱导导致了不同的蛋白质合成改变模式。我们观察到三种分子量分别为27 kDa、47 kDa和52 kDa的蛋白质的合成速率发生了瞬时改变。只有47 kDa的蛋白质也受到癌蛋白的调控。ras和mos癌基因产物强烈诱导合成的一种蛋白质也受热休克诱导表达。

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