细胞衰老过程中基因表达和转录因子结合活性的调控。

M Meyyappan, P W Atadja, K T Riabowol
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引用次数: 36

摘要

人类二倍体成纤维细胞(HDFs)在体外经历有限数量的群体倍增,被广泛用作细胞衰老的模型。尽管越来越多的证据表明细胞衰老是基因表达改变的结果,但人们对衰老细胞中调节基因表达的转录因子的活性知之甚少。本文综述了细胞衰老过程中基因表达改变和转录因子作用的相关文献,重点研究了血清反应因子(SRF)。SRF在衰老的HDFs中被过度磷酸化,并且不能与c-fos启动子中的血清反应元件结合。在复制衰老过程中,差异磷酸化可能至少在一定程度上导致了SRF和其他转录因子活性的改变,以及随后在衰老HDFs中血清调节基因表达的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of gene expression and transcription factor binding activity during cellular aging.

Human diploid fibroblasts (HDFs) undergo a limited number of population doublings in vitro and are widely used as a model of cellular aging. Despite growing evidence that cellular aging occurs as a result of altered gene expression, little is known about the activity of transcription factors that regulate gene expression in aging cells. Here we survey the relevant literature regarding altered gene expression and the role of transcription factors during cellular aging, focusing upon the serum response factor (SRF). SRF is hyperphosphorylated in senescent HDFs and fails to bind to the serum-response element in the c-fos promoter. Differential phosphorylation during replicative aging may contribute, at least in part, to the altered activity of SRF and possibly other transcription factors and to subsequent changes in the expression of serum-regulated genes in senescent HDFs.

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