The logic of chromatin architecture and remodelling at promoters

被引:322
|
作者
Cairns, Bradley R. [1 ]
机构
[1] Univ Utah, Sch Med, Huntsman Canc Inst, Howard Hughes Med Inst,Dept Oncol Sci, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
HISTONE H2A VARIANT; GENOME-WIDE; SACCHAROMYCES-CEREVISIAE; NUCLEOSOME ORGANIZATION; GENE-EXPRESSION; ACTIVE CHROMATIN; PHO5; PROMOTER; YEAST; TRANSCRIPTION; ACETYLATION;
D O I
10.1038/nature08450
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
The regulation of gene transcription involves a dynamic balance between packaging regulatory sequences into chromatin and allowing transcriptional regulators access to these sequences. Access is restricted by the nucleosomes, but these can be repositioned or ejected by enzymes known as nucleosome remodellers. In addition, the DNA sequence can impart stiffness or curvature to the DNA, thereby affecting the position of nucleosomes on the DNA, influencing particular promoter 'architectures'. Recent genome-wide studies in yeast suggest that constitutive and regulated genes have architectures that differ in terms of nucleosome position, turnover, remodelling requirements and transcriptional noise.
引用
收藏
页码:193 / 198
页数:6
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