Human proteins that interact with RNA/DNA hybrids

Isabel X. Wang(Howard Hughes Medical Institute), Christopher Grunseich(National Institute of Neurological Disorders and Stroke), Jennifer E. Fox(Howard Hughes Medical Institute), Joshua Burdick(Howard Hughes Medical Institute), Zhengwei Zhu(University of Michigan), Niema Ravazian(Howard Hughes Medical Institute), Markus Hafner(National Institute of Arthritis and Musculoskeletal and Skin Diseases), Vivian G. Cheung(Howard Hughes Medical Institute)
Genome Research
August 14, 2018
Cited by 220Open Access
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Abstract

RNA/DNA hybrids form when RNA hybridizes with its template DNA generating a three-stranded structure known as the R-loop. Knowledge of how they form and resolve, as well as their functional roles, is limited. Here, by pull-down assays followed by mass spectrometry, we identified 803 proteins that bind to RNA/DNA hybrids. Because these proteins were identified using in vitro assays, we confirmed that they bind to R-loops in vivo. They include proteins that are involved in a variety of functions, including most steps of RNA processing. The proteins are enriched for K homology (KH) and helicase domains. Among them, more than 300 proteins preferred binding to hybrids than double-stranded DNA. These proteins serve as starting points for mechanistic studies to elucidate what RNA/DNA hybrids regulate and how they are regulated.


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