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鉴定一种参与心脏基因调控的新型血清反应因子辅因子。

Identification of a novel serum response factor cofactor in cardiac gene regulation.

作者信息

Zhang Xiaomin, Azhar Gohar, Zhong Ying, Wei Jeanne Y

机构信息

Donald W. Reynolds Department of Geriatrics, University of Arkansas for Medical Sciences and Geriatric Research, 4301 W. Markham #748, Little Rock, AR 72205, USA.

出版信息

J Biol Chem. 2004 Dec 31;279(53):55626-32. doi: 10.1074/jbc.M405945200. Epub 2004 Oct 18.

Abstract

The transcription factor serum response factor (SRF) plays an important role in the regulation of a variety of cardiac genes during development and during adult aging. A novel SRF cofactor, herein called p49/STRAP, for SRF-dependent transcription regulation-associated protein, was recently identified in our laboratory. This protein interacted mainly with the transcriptional activation domain of the SRF protein and was found to bind to SRF or to the complex of SRF and another cofactor, such as myocardin or Nkx2.5. The expression of p49/STRAP affected the promoter activity of SRF target genes in a non-uniform manner. For example, p49 activated MLC2v and cardiac actin promoters when it was co-transfected with SRF, but it repressed atrial natriuretic factor promoter activity, which was strongly induced by myocardin. The p49/STRAP mRNA was observed to be highly expressed in fetal, adult, and senescent human hearts, and also in hearts of young adult and old mice, suggesting that p49/STRAP may be an important SRF cofactor in the transcriptional regulation of mammalian cardiac muscle genes throughout the life span.

摘要

转录因子血清反应因子(SRF)在心脏发育和成年期衰老过程中对多种心脏基因的调控起着重要作用。最近,我们实验室鉴定出一种新的SRF辅因子,在此称为p49/STRAP,即与SRF依赖性转录调控相关蛋白。该蛋白主要与SRF蛋白的转录激活域相互作用,并且被发现可与SRF或SRF与另一种辅因子(如心肌肌动蛋白或Nkx2.5)的复合物结合。p49/STRAP的表达以非均匀方式影响SRF靶基因的启动子活性。例如,当p49与SRF共转染时,它可激活MLC2v和心肌肌动蛋白启动子,但它会抑制心房利钠因子启动子活性,而该活性会被心肌肌动蛋白强烈诱导。观察到p49/STRAP mRNA在胎儿、成人和衰老的人类心脏中以及年轻成年和老年小鼠的心脏中均高度表达,这表明p49/STRAP可能是哺乳动物心肌基因在整个生命周期转录调控中一种重要的SRF辅因子。

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