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ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters
The 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 ZC3H...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023261/ https://www.ncbi.nlm.nih.gov/pubmed/35325203 http://dx.doi.org/10.1093/nar/gkac193 |
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author | Park, Kihyun Zhong, Jian Jang, Jin Sung Kim, Jihyun Kim, Hye-Jung Lee, Jeong-Heon Kim, Jaehoon |
author_facet | Park, Kihyun Zhong, Jian Jang, Jin Sung Kim, Jihyun Kim, Hye-Jung Lee, Jeong-Heon Kim, Jaehoon |
author_sort | Park, Kihyun |
collection | PubMed |
description | The 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. |
format | Online Article Text |
id | pubmed-9023261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90232612022-04-22 ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters Park, Kihyun Zhong, Jian Jang, Jin Sung Kim, Jihyun Kim, Hye-Jung Lee, Jeong-Heon Kim, Jaehoon Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The 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. Oxford University Press 2022-03-23 /pmc/articles/PMC9023261/ /pubmed/35325203 http://dx.doi.org/10.1093/nar/gkac193 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Park, Kihyun Zhong, Jian Jang, Jin Sung Kim, Jihyun Kim, Hye-Jung Lee, Jeong-Heon Kim, Jaehoon ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters |
title | ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters |
title_full | ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters |
title_fullStr | ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters |
title_full_unstemmed | ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters |
title_short | ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters |
title_sort | zwc complex-mediated spt5 phosphorylation suppresses divergent antisense rna transcription at active gene promoters |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023261/ https://www.ncbi.nlm.nih.gov/pubmed/35325203 http://dx.doi.org/10.1093/nar/gkac193 |
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