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A breaking strategy for topoisomerase IIbeta/PARP-1-dependent regulated transcription.

机译:拓扑异构酶IIbeta / PARP-1依赖性调节转录的突破策略。

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摘要

While diverse enzymatic activities are required for transcriptional initiation, a central question remains whether additional enzymatic activities involved in other cellular processes may also be critical for regulated gene activation. Recently, we reported that signal-dependent activation of gene transcription requires topoisomerase IIbeta (Topo IIbeta)-dependent, nucleosome-specific, transient double-stranded DNA break formation with subsequent activation of poly(ADP-ribose) polymerase-1 (PARP-1) enzymatic function, which causes local changes of chromatin architecture (Ju et al., Science 2006; 312:1798-802). Here, we discussed that possible molecular mechanism underling Topo IIbeta/PARP-1/DNA-PK network in transcriptional initiation and many intriguing issues remain to be solved in the future.
机译:虽然转录启动需要多种酶促活性,但仍然存在一个中心问题,即其他细胞过程中涉及的其他酶促活性对于调节基因激活是否也很关键。最近,我们报道了基因转录的信号依赖性激活需要拓扑异构酶IIbeta(Topo IIbeta)依赖性,核小体特异性,瞬时双链DNA断裂形成以及随后的poly(ADP-核糖)聚合酶-1(PARP-1)的激活酶功能,其导致染色质结构的局部改变(Ju等,Science 2006; 312:1798-802)。在这里,我们讨论了转录起始中Topo IIbeta / PARP-1 / DNA-PK网络基础的可能分子机制,并且许多有趣的问题在将来仍需解决。

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