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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
来源:
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.
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页码:2557 / 2560
页数:4
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