ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters

Author:

Park Kihyun1,Zhong Jian2,Jang Jin Sung34,Kim Jihyun1,Kim Hye-Jung5,Lee Jeong-Heon246,Kim Jaehoon1ORCID

Affiliation:

1. Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, South Korea

2. Epigenomics Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA

3. Medical Genome Facility, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA

4. Division of Experimental Pathology and Laboratory Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA

5. New Drug Development Center, OSONG Medical Innovation Foundation, Cheongju 28160, South Korea

6. Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA

Abstract

AbstractThe human genome encodes large numbers of non-coding RNAs, including divergent antisense transcripts at transcription start sites (TSSs). However, molecular mechanisms by which divergent antisense transcription is regulated have not been detailed. Here, we report a novel ZWC complex composed of ZC3H4, WDR82 and CK2 that suppresses divergent antisense transcription. The ZWC complex preferentially localizes at TSSs of active genes through direct interactions of ZC3H4 and WDR82 subunits with the S5p RNAPII C-terminal domain. ZC3H4 depletion leads to increased divergent antisense transcription, especially at genes that naturally produce divergent antisense transcripts. We further demonstrate that the ZWC complex phosphorylates the previously uncharacterized N-terminal acidic domain of SPT5, a subunit of the transcription-elongation factor DSIF, and that this phosphorylation is responsible for suppressing divergent antisense transcription. Our study provides evidence that the newly identified ZWC-DSIF axis regulates the direction of transcription during the transition from early to productive elongation.

Funder

National Research Foundation of Korea

National Institutes of Health

Mayo Clinic Center for Individualized Medicine

Publisher

Oxford University Press (OUP)

Subject

Genetics

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