Suppr超能文献

Fos蛋白C端突变可阻断血清刺激后c-fos转录的下调。

Fos C-terminal mutations block down-regulation of c-fos transcription following serum stimulation.

作者信息

Wilson T, Treisman R

机构信息

MRC Laboratory of Molecular Biology, MRC Centre, Cambridge, UK.

出版信息

EMBO J. 1988 Dec 20;7(13):4193-202. doi: 10.1002/j.1460-2075.1988.tb03316.x.

Abstract

Transient accumulation of c-fos RNA following serum stimulation requires both a conserved 5' regulatory element and sequences at the 3' end of the gene. Here we show that mutations at the C terminus of Fos protein, of the type found in a virally-transduced actively transforming Fos variant, prevent the rapid down-regulation of c-fos transcription that occurs following serum-induced activation. Fos mutants that prevent down-regulation are dominant, acting in trans to prevent down-regulation of a co-transfected c-fos gene. Co-transfection experiments suggest that this effect is mediated by multiple sequence elements in the 5'-flanking region. Analysis of different Fos mutants showed that replacement of Fos sequences C-terminal to amino acid 337 with heterologous polypeptide, rather than simple truncation of the protein, is required to produce mutants defective in down-regulation. The results are discussed with reference to transformation by Fos.

摘要

血清刺激后c-fos RNA的瞬时积累需要一个保守的5'调控元件和该基因3'端的序列。我们在此表明,在病毒转导的活跃转化Fos变体中发现的那种Fos蛋白C末端突变,会阻止血清诱导激活后发生的c-fos转录的快速下调。阻止下调的Fos突变体具有显性作用,可通过反式作用阻止共转染的c-fos基因的下调。共转染实验表明,这种效应是由5'侧翼区域中的多个序列元件介导的。对不同Fos突变体的分析表明,要用异源多肽取代Fos蛋白337位氨基酸C末端的序列,而不是简单地截短该蛋白,才能产生下调缺陷的突变体。我们结合Fos的转化作用对这些结果进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea9/455132/4f7570bad20b/emboj00150-0170-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验