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

被引:47
作者
Ju, Bong-Gun [1 ]
Rosenfeld, Michael G. [1 ]
机构
[1] Univ Calif San Diego, Sch Med, Howard Hughes Med Inst, Dept Mol Med, La Jolla, CA 92093 USA
关键词
transcription; tortional stress; DSB; topoisomerase II; PARP-1; DNA-PK; nuclear matrix;
D O I
10.4161/cc.5.22.3497
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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 II beta ( Topo II beta)-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 II beta/PARP-1/DNA-PK network in transcriptional initiation and many intriguing issues remain to be solved in the future.
引用
收藏
页码:2557 / 2560
页数:4
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