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

Author:

Bell Jason C1ORCID,Jukam David2ORCID,Teran Nicole A13ORCID,Risca Viviana I3ORCID,Smith Owen K14ORCID,Johnson Whitney L1,Skotheim Jan M2,Greenleaf William James35,Straight Aaron F14ORCID

Affiliation:

1. Department of Biochemistry, Stanford University, Stanford, United States

2. Department of Biology, Stanford University, Stanford, United States

3. Department of Genetics, Stanford University, Stanford, United States

4. Department of Chemical and Systems Biology, Stanford University, Stanford, United States

5. Department of Applied Physics, Stanford University, Stanford, United States

Abstract

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.

Funder

National Institutes of Health

Stanford University School of Medicine

Stanford University

National Science Foundation

Howard Hughes Medical Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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