Cargando…
Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos
N(6)-methyladenosine (m(6)A) on chromosome-associated regulatory RNAs (carRNAs), including repeat RNAs, plays important roles in tuning the chromatin state and transcription, but the intrinsic mechanism remains unclear. Here, we report that YTHDC1 plays indispensable roles in the self-renewal and di...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Higher Education Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160034/ https://www.ncbi.nlm.nih.gov/pubmed/33886094 http://dx.doi.org/10.1007/s13238-021-00837-8 |
_version_ | 1783700197707087872 |
---|---|
author | Chen, Chuan Liu, Wenqiang Guo, Jiayin Liu, Yuanyuan Liu, Xuelian Liu, Jun Dou, Xiaoyang Le, Rongrong Huang, Yixin Li, Chong Yang, Lingyue Kou, Xiaochen Zhao, Yanhong Wu, You Chen, Jiayu Wang, Hong Shen, Bin Gao, Yawei Gao, Shaorong |
author_facet | Chen, Chuan Liu, Wenqiang Guo, Jiayin Liu, Yuanyuan Liu, Xuelian Liu, Jun Dou, Xiaoyang Le, Rongrong Huang, Yixin Li, Chong Yang, Lingyue Kou, Xiaochen Zhao, Yanhong Wu, You Chen, Jiayu Wang, Hong Shen, Bin Gao, Yawei Gao, Shaorong |
author_sort | Chen, Chuan |
collection | PubMed |
description | N(6)-methyladenosine (m(6)A) on chromosome-associated regulatory RNAs (carRNAs), including repeat RNAs, plays important roles in tuning the chromatin state and transcription, but the intrinsic mechanism remains unclear. Here, we report that YTHDC1 plays indispensable roles in the self-renewal and differentiation potency of mouse embryonic stem cells (ESCs), which highly depends on the m(6)A-binding ability. Ythdc1 is required for sufficient rRNA synthesis and repression of the 2-cell (2C) transcriptional program in ESCs, which recapitulates the transcriptome regulation by the LINE1 scaffold. Detailed analyses revealed that YTHDC1 recognizes m(6)A on LINE1 RNAs in the nucleus and regulates the formation of the LINE1-NCL partnership and the chromatin recruitment of KAP1. Moreover, the establishment of H3K9me3 on 2C-related retrotransposons is interrupted in Ythdc1-depleted ESCs and inner cell mass (ICM) cells, which consequently increases the transcriptional activities. Our study reveals a role of m(6)A in regulating the RNA scaffold, providing a new model for the RNA-chromatin cross-talk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13238-021-00837-8. |
format | Online Article Text |
id | pubmed-8160034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Higher Education Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81600342021-06-17 Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos Chen, Chuan Liu, Wenqiang Guo, Jiayin Liu, Yuanyuan Liu, Xuelian Liu, Jun Dou, Xiaoyang Le, Rongrong Huang, Yixin Li, Chong Yang, Lingyue Kou, Xiaochen Zhao, Yanhong Wu, You Chen, Jiayu Wang, Hong Shen, Bin Gao, Yawei Gao, Shaorong Protein Cell Research Article N(6)-methyladenosine (m(6)A) on chromosome-associated regulatory RNAs (carRNAs), including repeat RNAs, plays important roles in tuning the chromatin state and transcription, but the intrinsic mechanism remains unclear. Here, we report that YTHDC1 plays indispensable roles in the self-renewal and differentiation potency of mouse embryonic stem cells (ESCs), which highly depends on the m(6)A-binding ability. Ythdc1 is required for sufficient rRNA synthesis and repression of the 2-cell (2C) transcriptional program in ESCs, which recapitulates the transcriptome regulation by the LINE1 scaffold. Detailed analyses revealed that YTHDC1 recognizes m(6)A on LINE1 RNAs in the nucleus and regulates the formation of the LINE1-NCL partnership and the chromatin recruitment of KAP1. Moreover, the establishment of H3K9me3 on 2C-related retrotransposons is interrupted in Ythdc1-depleted ESCs and inner cell mass (ICM) cells, which consequently increases the transcriptional activities. Our study reveals a role of m(6)A in regulating the RNA scaffold, providing a new model for the RNA-chromatin cross-talk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13238-021-00837-8. Higher Education Press 2021-04-22 2021-06 /pmc/articles/PMC8160034/ /pubmed/33886094 http://dx.doi.org/10.1007/s13238-021-00837-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Chen, Chuan Liu, Wenqiang Guo, Jiayin Liu, Yuanyuan Liu, Xuelian Liu, Jun Dou, Xiaoyang Le, Rongrong Huang, Yixin Li, Chong Yang, Lingyue Kou, Xiaochen Zhao, Yanhong Wu, You Chen, Jiayu Wang, Hong Shen, Bin Gao, Yawei Gao, Shaorong Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos |
title | Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos |
title_full | Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos |
title_fullStr | Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos |
title_full_unstemmed | Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos |
title_short | Nuclear m(6)A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos |
title_sort | nuclear m(6)a reader ythdc1 regulates the scaffold function of line1 rna in mouse escs and early embryos |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160034/ https://www.ncbi.nlm.nih.gov/pubmed/33886094 http://dx.doi.org/10.1007/s13238-021-00837-8 |
work_keys_str_mv | AT chenchuan nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT liuwenqiang nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT guojiayin nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT liuyuanyuan nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT liuxuelian nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT liujun nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT douxiaoyang nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT lerongrong nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT huangyixin nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT lichong nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT yanglingyue nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT kouxiaochen nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT zhaoyanhong nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT wuyou nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT chenjiayu nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT wanghong nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT shenbin nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT gaoyawei nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos AT gaoshaorong nuclearm6areaderythdc1regulatesthescaffoldfunctionofline1rnainmouseescsandearlyembryos |