Chromatin-associated RNA sequencing (ChAR-seq) maps genome-wide RNA-to-DNA contacts

被引:111
作者
Bell, Jason C. [1 ,6 ]
Jukam, David [2 ]
Teran, Nicole A. [1 ,3 ]
Risca, Viviana I. [3 ]
Smith, Owen K. [1 ,4 ]
Johnson, Whitney L. [1 ]
Skotheim, Jan M. [2 ]
Greenleaf, William James [3 ,5 ]
Straight, Aaron F. [1 ,4 ]
机构
[1] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Chem & Syst Biol, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[6] 10x Genomics, Mol Biol, Pleasanton, CA 94566 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
NONCODING RNA; DROSOPHILA-MELANOGASTER; MSL COMPLEX; TRANSCRIPTION ELONGATION; DOSAGE COMPENSATION; REGULATORY ELEMENTS; ACTIVE CHROMATIN; GENE-EXPRESSION; X-CHROMOSOME; IN-VIVO;
D O I
10.7554/eLife.27024
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNA is a critical component of chromatin in eukaryotes, both as a product of transcription, and as an essential constituent of ribonucleoprotein complexes that regulate both local and global chromatin states. Here, we present a proximity ligation and sequencing method called Chromatin-Associated RNA sequencing (ChAR-seq) that maps all RNA-to-DNA contacts across the genome. Using Drosophila cells, we show that ChAR-seq provides unbiased, de novo identification of targets of chromatin-bound RNAs including nascent transcripts, chromosome-specific dosage compensation ncRNAs, and genome-wide trans-associated RNAs involved in co-transcriptional RNA processing.
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页数:28
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