Ju Bong-Gun, Rosenfeld Michael G
Howard Hughes Medical Institute, Department of Molecular Medicine, School of Medicine, University of California, San Diego, La Jolla, California 92093-0648, USA.
Cell Cycle. 2006 Nov;5(22):2557-60. doi: 10.4161/cc.5.22.3497. Epub 2006 Nov 15.
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.
虽然转录起始需要多种酶活性,但一个核心问题仍然存在:参与其他细胞过程的额外酶活性是否对基因激活调控也至关重要。最近,我们报道基因转录的信号依赖性激活需要拓扑异构酶IIβ(Topo IIβ)依赖性、核小体特异性、瞬时双链DNA断裂形成,随后激活聚(ADP-核糖)聚合酶-1(PARP-1)的酶功能,这会导致染色质结构的局部变化(Ju等人,《科学》2006年;312:1798 - 1802)。在这里,我们讨论了Topo IIβ/PARP-1/DNA-PK网络在转录起始中的可能分子机制,并且未来仍有许多有趣的问题有待解决。