A topoisomerase IIβ-mediated dsDNA break required for regulated transcription

被引:694
作者
Ju, BG
Lunyak, VV
Perissi, V
Garcia-Bassets, I
Rose, DW
Glass, CK
Rosenfeld, MG
机构
[1] Univ Calif San Diego, Howard Hughes Med Inst, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, Div Endocrinol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sch Med, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
关键词
DEPENDENT PROTEIN-KINASE; ESTROGEN-RECEPTOR-ALPHA; RNA-POLYMERASE-II; POLY(ADP-RIBOSE) POLYMERASE; KAPPA-B; CHROMATIN-STRUCTURE; NUCLEAR RECEPTORS; ADP-RIBOSYLATION; BINDING PROTEIN; COACTIVATOR;
D O I
10.1126/science.1127196
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple enzymatic activities are required for transcriptional initiation. The enzyme DNA topoisomerase II associates with gene promoter regions and can generate breaks in double-stranded DNA (dsDNA). Therefore, it is of interest to know whether this enzyme is critical for regulated gene activation. We report that the signal-dependent activation of gene transcription by nuclear receptors and other classes of DNA binding transcription factors, including activating protein 1, requires DNA topoisomerase II beta-dependent, transient, site-specific dsDNA break formation. Subsequent to the break, poly( adenosine diphosphate-ribose) polymerase-1 enzymatic activity is induced, which is required for a nucleosome-specific histone H1-high-mobility group B exchange event and for local changes of chromatin architecture. Our data mechanistically link DNA topoisomerase IIb-dependent dsDNA breaks and the components of the DNA damage and repair machinery in regulated gene transcription.
引用
收藏
页码:1798 / 1802
页数:5
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