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Ageing and PARP.

机译:老化和PARP。

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摘要

Poly(ADP-ribosyl)ation, which is the posttranslational modification of proteins with poly(ADP-ribose), is catalysed by poly(ADP-ribose) polymerases. DNA-strand break induced catalytic activation of two PARP isoforms, namely PARP-1 and -2, are in involved in DNA base-excision repair and other repair pathways. A body of correlative data suggests a link between DNA-damage induced poly(ADP-ribosyl)ation and mammalian longevity. This notion was reinforced by recently published evidence for interactions between PARP-1 and the Werner syndrome protein, deficiency of which causes premature ageing in humans. Recent research on PARPs and poly(ADP-ribose) provides several candidate mechanisms through which poly(ADP-ribosyl)ation might contribute to keeping the ageing process at slow pace.
机译:聚(ADP-核糖)化是由聚(ADP-核糖)聚合酶催化的蛋白质用聚(ADP-核糖)的翻译后修饰。 DNA链断裂诱导的两种PARP亚型,即PARP-1和-2的催化活化涉及DNA碱基切除修复和其他修复途径。大量相关数据表明,DNA损伤诱导的聚(ADP-核糖基)化与哺乳动物寿命之间存在联系。最近发表的有关PARP-1与Werner综合征蛋白相互作用的证据进一步证实了这一观点,该蛋白的缺乏会导致人类过早衰老。最近对PARPs和聚(ADP-核糖)的研究提供了几种候选机制,通过这些机制,聚(ADP-核糖)可能有助于保持衰老过程的缓慢进行。

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