A RSC/Nucleosome Complex Determines Chromatin Architecture and Facilitates Activator Binding

被引:140
作者
Floer, Monique [1 ]
Wang, Xin [1 ]
Prabhu, Vidya [1 ]
Berrozpe, Georgina [1 ]
Narayan, Santosh [1 ]
Spagna, Dan [1 ]
Alvarez, David [1 ]
Kendall, Jude [2 ]
Krasnitz, Alexander [2 ]
Stepansky, Asya [2 ]
Hicks, James [2 ]
Bryant, Gene O. [1 ]
Ptashne, Mark [1 ]
机构
[1] Sloan Kettering Inst, Program Mol Biol, New York, NY 10021 USA
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
关键词
NUCLEOSOME OCCUPANCY; TRANSCRIPTION FACTOR; RSC; ORGANIZATION; LOCATION; PROMOTER; GENES; REPRESSION; TURNOVER; SEQUENCE;
D O I
10.1016/j.cell.2010.03.048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
How is chromatin architecture established and what role does it play in transcription? We show that the yeast regulatory locus UASg bears, in addition to binding sites for the activator Gal4, sites bound by the RSC complex. RSC positions a nucleosome, evidently partially unwound, in a structure that facilitates Gal4 binding to its sites. The complex comprises a barrier that imposes characteristic features of chromatin architecture. In the absence of RSC, ordinary nucleosomes encroach over the UASg and compete with Gal4 for binding. Taken with our previous work, the results show that both prior to and following induction, specific DNA-binding proteins are the predominant determinants of chromatin architecture at the GAL1/10 genes. RSC/nucleosome complexes are also found scattered around the yeast genome. Higher eukaryotic RSC lacks the specific DNA-binding determinants found on yeast RSC, and evidently Gal4 works in those organisms despite whatever obstacle broadly positioned nucleosomes present.
引用
收藏
页码:407 / 418
页数:12
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