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PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development
Growing oocytes store a large amount of maternal mRNA to support the subsequent “maternal-zygotic transition” process. At present, it is not clear how the growing oocytes store and process the newly transcribed mRNA under physiological conditions. In this study, we report non–membrane-bound compartm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616507/ https://www.ncbi.nlm.nih.gov/pubmed/36306357 http://dx.doi.org/10.1126/sciadv.abn9016 |
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author | Dai, Xing-Xing Pi, Shuai-Bo Zhao, Long-Wen Wu, Yun-Wen Shen, Jing-Ling Zhang, Song-Ying Sha, Qian-Qian Fan, Heng-Yu |
author_facet | Dai, Xing-Xing Pi, Shuai-Bo Zhao, Long-Wen Wu, Yun-Wen Shen, Jing-Ling Zhang, Song-Ying Sha, Qian-Qian Fan, Heng-Yu |
author_sort | Dai, Xing-Xing |
collection | PubMed |
description | Growing oocytes store a large amount of maternal mRNA to support the subsequent “maternal-zygotic transition” process. At present, it is not clear how the growing oocytes store and process the newly transcribed mRNA under physiological conditions. In this study, we report non–membrane-bound compartments, nuclear poly(A) domains (NPADs), as the hub for newly transcribed mRNA, in developing mouse oocytes. The RNA binding protein PABPN1 promotes the formation of NPAD through its N-terminal disordered domain and RNA-recognized motif by means of liquid phase separation. Pabpn1-null growing oocytes cannot form NPAD normally in vivo and have defects in stability of oocyte growing–related transcripts and formation of long 3′ untranslated region isoform transcripts. Ultimately, Pabpn1(fl/fl);Gdf9-Cre mice are completely sterile with primary ovarian insufficiency. These results demonstrate that NPAD formed by the phase separation properties of PABPN1-mRNA are the hub of the newly transcribed mRNA and essential for the development of oocytes and female reproduction. |
format | Online Article Text |
id | pubmed-9616507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96165072022-11-04 PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development Dai, Xing-Xing Pi, Shuai-Bo Zhao, Long-Wen Wu, Yun-Wen Shen, Jing-Ling Zhang, Song-Ying Sha, Qian-Qian Fan, Heng-Yu Sci Adv Biomedicine and Life Sciences Growing oocytes store a large amount of maternal mRNA to support the subsequent “maternal-zygotic transition” process. At present, it is not clear how the growing oocytes store and process the newly transcribed mRNA under physiological conditions. In this study, we report non–membrane-bound compartments, nuclear poly(A) domains (NPADs), as the hub for newly transcribed mRNA, in developing mouse oocytes. The RNA binding protein PABPN1 promotes the formation of NPAD through its N-terminal disordered domain and RNA-recognized motif by means of liquid phase separation. Pabpn1-null growing oocytes cannot form NPAD normally in vivo and have defects in stability of oocyte growing–related transcripts and formation of long 3′ untranslated region isoform transcripts. Ultimately, Pabpn1(fl/fl);Gdf9-Cre mice are completely sterile with primary ovarian insufficiency. These results demonstrate that NPAD formed by the phase separation properties of PABPN1-mRNA are the hub of the newly transcribed mRNA and essential for the development of oocytes and female reproduction. American Association for the Advancement of Science 2022-10-28 /pmc/articles/PMC9616507/ /pubmed/36306357 http://dx.doi.org/10.1126/sciadv.abn9016 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Dai, Xing-Xing Pi, Shuai-Bo Zhao, Long-Wen Wu, Yun-Wen Shen, Jing-Ling Zhang, Song-Ying Sha, Qian-Qian Fan, Heng-Yu PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development |
title | PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development |
title_full | PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development |
title_fullStr | PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development |
title_full_unstemmed | PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development |
title_short | PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development |
title_sort | pabpn1 functions as a hub in the assembly of nuclear poly(a) domains that are essential for mouse oocyte development |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616507/ https://www.ncbi.nlm.nih.gov/pubmed/36306357 http://dx.doi.org/10.1126/sciadv.abn9016 |
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