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Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation
Polycomb Repressive Complex 2 (PRC2) is an epigenetic regulator required for gene silencing during development. Although PRC2 is a well-established RNA-binding complex, the biological function of PRC2-RNA interaction has been controversial. Here, we study the gene-regulatory role of the inhibitory P...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001699/ https://www.ncbi.nlm.nih.gov/pubmed/35411071 http://dx.doi.org/10.1038/s42003-022-03250-x |
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author | Teo, Wei Wen Cao, Xinang Wu, Chan-Shuo Tan, Hong Kee Zhou, Qiling Gao, Chong Vanuytsel, Kim Kumar, Sara S. Murphy, George J. Yang, Henry Chai, Li Tenen, Daniel G. |
author_facet | Teo, Wei Wen Cao, Xinang Wu, Chan-Shuo Tan, Hong Kee Zhou, Qiling Gao, Chong Vanuytsel, Kim Kumar, Sara S. Murphy, George J. Yang, Henry Chai, Li Tenen, Daniel G. |
author_sort | Teo, Wei Wen |
collection | PubMed |
description | Polycomb Repressive Complex 2 (PRC2) is an epigenetic regulator required for gene silencing during development. Although PRC2 is a well-established RNA-binding complex, the biological function of PRC2-RNA interaction has been controversial. Here, we study the gene-regulatory role of the inhibitory PRC2-RNA interactions. We report a nuclear long non-coding RNA, LEVER, which mapped 236 kb upstream of the β-globin cluster as confirmed by Nanopore sequencing. LEVER RNA interacts with PRC2 in its nascent form, and this prevents the accumulation of the H3K27 repressive histone marks within LEVER locus. Interestingly, the accessible LEVER chromatin, in turn, suppresses the chromatin interactions between the ε-globin locus and β-globin locus control region (LCR), resulting in a repressive effect on ε-globin gene expression. Our findings validate that the nascent RNA-PRC2 interaction inhibits local PRC2 function in situ. More importantly, we demonstrate that such a local process can in turn regulate the expression of neighboring genes. |
format | Online Article Text |
id | pubmed-9001699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90016992022-04-27 Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation Teo, Wei Wen Cao, Xinang Wu, Chan-Shuo Tan, Hong Kee Zhou, Qiling Gao, Chong Vanuytsel, Kim Kumar, Sara S. Murphy, George J. Yang, Henry Chai, Li Tenen, Daniel G. Commun Biol Article Polycomb Repressive Complex 2 (PRC2) is an epigenetic regulator required for gene silencing during development. Although PRC2 is a well-established RNA-binding complex, the biological function of PRC2-RNA interaction has been controversial. Here, we study the gene-regulatory role of the inhibitory PRC2-RNA interactions. We report a nuclear long non-coding RNA, LEVER, which mapped 236 kb upstream of the β-globin cluster as confirmed by Nanopore sequencing. LEVER RNA interacts with PRC2 in its nascent form, and this prevents the accumulation of the H3K27 repressive histone marks within LEVER locus. Interestingly, the accessible LEVER chromatin, in turn, suppresses the chromatin interactions between the ε-globin locus and β-globin locus control region (LCR), resulting in a repressive effect on ε-globin gene expression. Our findings validate that the nascent RNA-PRC2 interaction inhibits local PRC2 function in situ. More importantly, we demonstrate that such a local process can in turn regulate the expression of neighboring genes. Nature Publishing Group UK 2022-04-11 /pmc/articles/PMC9001699/ /pubmed/35411071 http://dx.doi.org/10.1038/s42003-022-03250-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Teo, Wei Wen Cao, Xinang Wu, Chan-Shuo Tan, Hong Kee Zhou, Qiling Gao, Chong Vanuytsel, Kim Kumar, Sara S. Murphy, George J. Yang, Henry Chai, Li Tenen, Daniel G. Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation |
title | Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation |
title_full | Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation |
title_fullStr | Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation |
title_full_unstemmed | Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation |
title_short | Non-coding RNA LEVER sequestration of PRC2 can mediate long range gene regulation |
title_sort | non-coding rna lever sequestration of prc2 can mediate long range gene regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001699/ https://www.ncbi.nlm.nih.gov/pubmed/35411071 http://dx.doi.org/10.1038/s42003-022-03250-x |
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