A Packing Mechanism for Nucleosome Organization Reconstituted Across a Eukaryotic Genome

被引:244
|
作者
Zhang, Zhenhai [2 ]
Wippo, Christian J. [1 ]
Wal, Megha [2 ]
Ward, Elissa [2 ]
Korber, Philipp [1 ]
Pugh, B. Franklin [2 ]
机构
[1] Univ Munich, Adolf Butenandt Inst, D-80336 Munich, Germany
[2] Penn State Univ, Dept Biochem & Mol Biol, Ctr Eukaryot Gene Regulat, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
POSITIONS IN-VIVO; SACCHAROMYCES-CEREVISIAE; REMODELING FACTOR; DNA-SEQUENCE; PROMOTER; YEAST; TRANSCRIPTION; POLY(DA-DT); VITRO; ISWI;
D O I
10.1126/science.1200508
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
Near the 5' end of most eukaryotic genes, nucleosomes form highly regular arrays that begin at canonical distances from the transcriptional start site. Determinants of this and other aspects of genomic nucleosome organization have been ascribed to statistical positioning, intrinsically DNA-encoded positioning, or some aspect of transcription initiation. Here, we provide evidence for a different explanation. Biochemical reconstitution of proper nucleosome positioning, spacing, and occupancy levels was achieved across the 5' ends of most yeast genes by adenosine triphosphate-dependent trans-acting factors. These transcription-independent activities override DNA-intrinsic positioning and maintain uniform spacing at the 5' ends of genes even at low nucleosome densities. Thus, an active, nonstatistical nucleosome packing mechanism creates chromatin organizing centers at the 5' ends of genes where important regulatory elements reside.
引用
收藏
页码:977 / 980
页数:4
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