Genome-Wide Views of Chromatin Structure

被引:235
作者
Rando, Oliver J. [1 ]
Chang, Howard Y. [2 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01605 USA
[2] Stanford Univ, Program Epithelial Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
epigenetics; gene regulation; histone modifications; microarray; nucleosome; RNA-POLYMERASE-II; EMBRYONIC STEM-CELLS; HISTONE H3 EXCHANGE; HIGH-RESOLUTION MAP; SACCHAROMYCES-CEREVISIAE; IN-VIVO; TRANSCRIPTION INITIATION; NUCLEOSOME OCCUPANCY; DYNAMIC REGULATION; NONCODING RNAS;
D O I
10.1146/annurev.biochem.78.071107.134639
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
Eukaryotic genomes are package into a nucleoprotein complex known as chromatin, which affects most processes that occur on DNA. Along with genetic and biochemical studies of resident chromatin proteins and their modifying enzymes, mapping of chromatin structure in vivo is one of the main pillars in our understanding of how chromatin relates to cellular processes. M this review, we discuss the use of genomic technologies to characterize chromatin structure in vivo, with a focus on data from budding yeast and humans. The picture emerging from these studies is the detailed chromatin structure of a typical gene, where the typical behavior gives insight into the mechanisms and deep rules that establish chromatin structure. Important deviation from the archetype is also observed, usually as a consequence of unique regulatory mechanisms at special genomic loci. Chromatin structure shows substantial conservation from yeast to humans, but mammalian chromatin has additional layers of complexity that likely relate to the requirements of multicellularity such as the need to establish faithful gene regulatory mechanisms for cell differentiation.
引用
收藏
页码:245 / 271
页数:27
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