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首页> 外文期刊>World Journal of Gastroenterology >Effects of histone acetylation and DNA methylation on p21~(WAF1) regulation
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Effects of histone acetylation and DNA methylation on p21~(WAF1) regulation

机译:组蛋白乙酰化和DNA甲基化对p21〜(WAF1)调节的影响

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摘要

Cell cycle progression is regulated by interactions cyclins and cyclin-dependent kinases (CDKs). p21~(WAF1) is one of the CIP/KIP family which inhibits CDKs activity. Increased expression of p21~(WAF1) may play an important role in the growth arrest induced in transformed cells. Although the stability of the p21~(WAF1) mRNA could be altered by different signals, cell differentiation and numerous influencing factors. However, recent studies suggest that two known mechanisms of epigenesis, i. e. gene inactivation by methylation in promoter region and changes to an inactive chromatin by histone deacetylation, seem to be the best candidate mechanisms for inactivation of p21~(WAF1).
机译:细胞周期进程受细胞周期蛋白和细胞周期蛋白依赖性激酶(CDKs)相互作用的调节。 p21〜(WAF1)是抑制CDK活性的CIP / KIP家族之一。 p21〜(WAF1)的表达增加可能在转化细胞诱导的生长停滞中起重要作用。尽管p21〜(WAF1)mRNA的稳定性可以通过不同的信号,细胞分化和许多影响因素来改变。然而,最近的研究表明表观遗传的两种已知机制,即表观遗传。 e。启动子区域甲基化引起的基因失活以及组蛋白脱乙酰基化而使染色质失活,似乎是p21〜(WAF1)失活的最佳候选机制。

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