Genomic Maps of Long Noncoding RNA Occupancy Reveal Principles of RNA-Chromatin Interactions

被引:980
作者
Chu, Ci [1 ,2 ]
Qu, Kun [1 ,2 ]
Zhong, Franklin L. [3 ]
Artandi, Steven E. [3 ]
Chang, Howard Y. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Program Epithelial Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA
关键词
POLYCOMB RESPONSE ELEMENT; DOSAGE COMPENSATION; X-CHROMOSOME; GENE-EXPRESSION; IN-VIVO; DROSOPHILA; TELOMERASE; COMPLEXES; PROTEINS; SCAFFOLD;
D O I
10.1016/j.molcel.2011.08.027
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
Long noncoding RNAs (IncRNAs) are key regulators of chromatin state, yet the nature and sites of RNA-chromatin interaction are mostly unknown. Here we introduce Chromatin Isolation by RNA Purification (ChIRP), where tiling oligonucleotides retrieve specific IncRNAs with bound protein and DNA sequences, which are enumerated by deep sequencing. ChIRP-seq of three IncRNAs reveal that RNA occupancy sites in the genome are focal, sequence-specific, and numerous. Drosophila roX2 RNA occupies male X-linked gene bodies with increasing tendency toward the 3' end, peaking at CES sites. Human telomerase RNA TERC occupies telomeres and Writ pathway genes. HOTAIR IncRNA preferentially occupies a GA-rich DNA motif to nucleate broad domains of Polycomb occupancy and histone H3 lysine 27 trimethylation. HOTAIR occupancy occur; independently of EZH2, suggesting the order of RNA guidance of Polycomb occupancy. ChIRP-seq is generally applicable to illuminate the intersection of RNA and chromatin with newfound precision genome wide.
引用
收藏
页码:667 / 678
页数:12
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