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A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility
Changes in ambient temperature influence crop fertility and production. Understanding of how crops sense and respond to temperature is thus crucial for sustainable agriculture. The thermosensitive genic male-sterile (TGMS) lines are widely used for hybrid rice breeding and also provide a good system...
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/PMC9018702/ https://www.ncbi.nlm.nih.gov/pubmed/35440626 http://dx.doi.org/10.1038/s41467-022-29648-z |
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author | Wu, Lunying Jing, Xiaohui Zhang, Baolan Chen, Shoujun Xu, Ran Duan, Penggen Zou, Danni Huang, Shengjian Zhou, Tingbo An, Chengcai Luo, Yuehua Li, Yunhai |
author_facet | Wu, Lunying Jing, Xiaohui Zhang, Baolan Chen, Shoujun Xu, Ran Duan, Penggen Zou, Danni Huang, Shengjian Zhou, Tingbo An, Chengcai Luo, Yuehua Li, Yunhai |
author_sort | Wu, Lunying |
collection | PubMed |
description | Changes in ambient temperature influence crop fertility and production. Understanding of how crops sense and respond to temperature is thus crucial for sustainable agriculture. The thermosensitive genic male-sterile (TGMS) lines are widely used for hybrid rice breeding and also provide a good system to investigate the mechanisms underlying temperature sensing and responses in crops. Here, we show that OsMS1 is a histone binding protein, and its natural allele OsMS1(wenmin1) confers thermosensitive male sterility in rice. OsMS1 is primarily localized in nuclei, while OsMS1(wenmin1) is localized in nuclei and cytoplasm. Temperature regulates the abundances of OsMS1 and OsMS1(wenmin1) proteins. The high temperature causes more reduction of OsMS1(wenmin1) than OsMS1 in nuclei. OsMS1 associates with the transcription factor TDR to regulate expression of downstream genes in a temperature-dependent manner. Thus, our findings uncover a thermosensitive mechanism that could be useful for hybrid crop breeding. |
format | Online Article Text |
id | pubmed-9018702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90187022022-04-28 A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility Wu, Lunying Jing, Xiaohui Zhang, Baolan Chen, Shoujun Xu, Ran Duan, Penggen Zou, Danni Huang, Shengjian Zhou, Tingbo An, Chengcai Luo, Yuehua Li, Yunhai Nat Commun Article Changes in ambient temperature influence crop fertility and production. Understanding of how crops sense and respond to temperature is thus crucial for sustainable agriculture. The thermosensitive genic male-sterile (TGMS) lines are widely used for hybrid rice breeding and also provide a good system to investigate the mechanisms underlying temperature sensing and responses in crops. Here, we show that OsMS1 is a histone binding protein, and its natural allele OsMS1(wenmin1) confers thermosensitive male sterility in rice. OsMS1 is primarily localized in nuclei, while OsMS1(wenmin1) is localized in nuclei and cytoplasm. Temperature regulates the abundances of OsMS1 and OsMS1(wenmin1) proteins. The high temperature causes more reduction of OsMS1(wenmin1) than OsMS1 in nuclei. OsMS1 associates with the transcription factor TDR to regulate expression of downstream genes in a temperature-dependent manner. Thus, our findings uncover a thermosensitive mechanism that could be useful for hybrid crop breeding. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9018702/ /pubmed/35440626 http://dx.doi.org/10.1038/s41467-022-29648-z 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 Wu, Lunying Jing, Xiaohui Zhang, Baolan Chen, Shoujun Xu, Ran Duan, Penggen Zou, Danni Huang, Shengjian Zhou, Tingbo An, Chengcai Luo, Yuehua Li, Yunhai A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility |
title | A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility |
title_full | A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility |
title_fullStr | A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility |
title_full_unstemmed | A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility |
title_short | A natural allele of OsMS1 responds to temperature changes and confers thermosensitive genic male sterility |
title_sort | natural allele of osms1 responds to temperature changes and confers thermosensitive genic male sterility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018702/ https://www.ncbi.nlm.nih.gov/pubmed/35440626 http://dx.doi.org/10.1038/s41467-022-29648-z |
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