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Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation
Zygotic genome activation (ZGA) is essential for early embryonic development. However, the regulation of ZGA remains elusive in mammals. Here we report that a maternal factor TDP-43, a nuclear transactive response DNA-binding protein, regulates ZGA through RNA Pol II and is essential for mouse early...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352294/ https://www.ncbi.nlm.nih.gov/pubmed/37460529 http://dx.doi.org/10.1038/s41467-023-39924-1 |
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author | Nie, Xiaoqing Xu, Qianhua Xu, Chengpeng Chen, Fengling Wang, Qizhi Qin, Dandan Wang, Rui Gao, Zheng Lu, Xukun Yang, Xinai Wu, Yu Gu, Chen Xie, Wei Li, Lei |
author_facet | Nie, Xiaoqing Xu, Qianhua Xu, Chengpeng Chen, Fengling Wang, Qizhi Qin, Dandan Wang, Rui Gao, Zheng Lu, Xukun Yang, Xinai Wu, Yu Gu, Chen Xie, Wei Li, Lei |
author_sort | Nie, Xiaoqing |
collection | PubMed |
description | Zygotic genome activation (ZGA) is essential for early embryonic development. However, the regulation of ZGA remains elusive in mammals. Here we report that a maternal factor TDP-43, a nuclear transactive response DNA-binding protein, regulates ZGA through RNA Pol II and is essential for mouse early embryogenesis. Maternal TDP-43 translocates from the cytoplasm into the nucleus at the early two-cell stage when minor to major ZGA transition occurs. Genetic deletion of maternal TDP-43 results in mouse early embryos arrested at the two-cell stage. TDP-43 co-occupies with RNA Pol II as large foci in the nucleus and also at the promoters of ZGA genes at the late two-cell stage. Biochemical evidence indicates that TDP-43 binds Polr2a and Cyclin T1. Depletion of maternal TDP-43 caused the loss of Pol II foci and reduced Pol II binding on chromatin at major ZGA genes, accompanied by defective ZGA. Collectively, our results suggest that maternal TDP-43 is critical for mouse early embryonic development, in part through facilitating the correct RNA Pol II configuration and zygotic genome activation. |
format | Online Article Text |
id | pubmed-10352294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103522942023-07-19 Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation Nie, Xiaoqing Xu, Qianhua Xu, Chengpeng Chen, Fengling Wang, Qizhi Qin, Dandan Wang, Rui Gao, Zheng Lu, Xukun Yang, Xinai Wu, Yu Gu, Chen Xie, Wei Li, Lei Nat Commun Article Zygotic genome activation (ZGA) is essential for early embryonic development. However, the regulation of ZGA remains elusive in mammals. Here we report that a maternal factor TDP-43, a nuclear transactive response DNA-binding protein, regulates ZGA through RNA Pol II and is essential for mouse early embryogenesis. Maternal TDP-43 translocates from the cytoplasm into the nucleus at the early two-cell stage when minor to major ZGA transition occurs. Genetic deletion of maternal TDP-43 results in mouse early embryos arrested at the two-cell stage. TDP-43 co-occupies with RNA Pol II as large foci in the nucleus and also at the promoters of ZGA genes at the late two-cell stage. Biochemical evidence indicates that TDP-43 binds Polr2a and Cyclin T1. Depletion of maternal TDP-43 caused the loss of Pol II foci and reduced Pol II binding on chromatin at major ZGA genes, accompanied by defective ZGA. Collectively, our results suggest that maternal TDP-43 is critical for mouse early embryonic development, in part through facilitating the correct RNA Pol II configuration and zygotic genome activation. Nature Publishing Group UK 2023-07-17 /pmc/articles/PMC10352294/ /pubmed/37460529 http://dx.doi.org/10.1038/s41467-023-39924-1 Text en © The Author(s) 2023 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 Nie, Xiaoqing Xu, Qianhua Xu, Chengpeng Chen, Fengling Wang, Qizhi Qin, Dandan Wang, Rui Gao, Zheng Lu, Xukun Yang, Xinai Wu, Yu Gu, Chen Xie, Wei Li, Lei Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation |
title | Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation |
title_full | Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation |
title_fullStr | Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation |
title_full_unstemmed | Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation |
title_short | Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation |
title_sort | maternal tdp-43 interacts with rna pol ii and regulates zygotic genome activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352294/ https://www.ncbi.nlm.nih.gov/pubmed/37460529 http://dx.doi.org/10.1038/s41467-023-39924-1 |
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