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OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development

Meiosis plays an essential role in the production of gametes and genetic diversity of posterities. The normal double-strand break (DSB) repair is vital to homologous recombination (HR) and occurrence of DNA fragment exchange, but the underlying molecular mechanism remain elusive. Here, we characteri...

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Autores principales: Lu, Jiayu, Wang, Chaolong, Wang, Haiyu, Zheng, Hai, Bai, Wenting, Lei, Dekun, Tian, Yunlu, Xiao, Yanjia, You, Shimin, Wang, Qiming, Yu, Xiaowen, Liu, Shijia, Liu, Xi, Chen, Liangming, Jang, Ling, Wang, Chunming, Zhao, Zhigang, Wan, Jianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243175/
https://www.ncbi.nlm.nih.gov/pubmed/32499797
http://dx.doi.org/10.3389/fpls.2020.00518
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author Lu, Jiayu
Wang, Chaolong
Wang, Haiyu
Zheng, Hai
Bai, Wenting
Lei, Dekun
Tian, Yunlu
Xiao, Yanjia
You, Shimin
Wang, Qiming
Yu, Xiaowen
Liu, Shijia
Liu, Xi
Chen, Liangming
Jang, Ling
Wang, Chunming
Zhao, Zhigang
Wan, Jianmin
author_facet Lu, Jiayu
Wang, Chaolong
Wang, Haiyu
Zheng, Hai
Bai, Wenting
Lei, Dekun
Tian, Yunlu
Xiao, Yanjia
You, Shimin
Wang, Qiming
Yu, Xiaowen
Liu, Shijia
Liu, Xi
Chen, Liangming
Jang, Ling
Wang, Chunming
Zhao, Zhigang
Wan, Jianmin
author_sort Lu, Jiayu
collection PubMed
description Meiosis plays an essential role in the production of gametes and genetic diversity of posterities. The normal double-strand break (DSB) repair is vital to homologous recombination (HR) and occurrence of DNA fragment exchange, but the underlying molecular mechanism remain elusive. Here, we characterized a completely sterile Osmfs1 (male and female sterility 1) mutant which has its pollen and embryo sacs both aborted at the reproductive stage due to severe chromosome defection. Map-based cloning revealed that the OsMFS1 encodes a meiotic coiled-coil protein, and it is responsible for DSB repairing that acts as an important cofactor to stimulate the single strand invasion. Expression pattern analyses showed the OsMFS1 was preferentially expressed in meiosis stage. Subcellular localization analysis of OsMFS1 revealed its association with the nucleus exclusively. In addition, a yeast two-hybrid (Y2H) and pull-down assay showed that OsMFS1 could physically interact with OsHOP2 protein to form a stable complex to ensure faithful homologous recombination. Taken together, our results indicated that OsMFS1 is indispensable to the normal development of anther and embryo sacs in rice.
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spelling pubmed-72431752020-06-03 OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development Lu, Jiayu Wang, Chaolong Wang, Haiyu Zheng, Hai Bai, Wenting Lei, Dekun Tian, Yunlu Xiao, Yanjia You, Shimin Wang, Qiming Yu, Xiaowen Liu, Shijia Liu, Xi Chen, Liangming Jang, Ling Wang, Chunming Zhao, Zhigang Wan, Jianmin Front Plant Sci Plant Science Meiosis plays an essential role in the production of gametes and genetic diversity of posterities. The normal double-strand break (DSB) repair is vital to homologous recombination (HR) and occurrence of DNA fragment exchange, but the underlying molecular mechanism remain elusive. Here, we characterized a completely sterile Osmfs1 (male and female sterility 1) mutant which has its pollen and embryo sacs both aborted at the reproductive stage due to severe chromosome defection. Map-based cloning revealed that the OsMFS1 encodes a meiotic coiled-coil protein, and it is responsible for DSB repairing that acts as an important cofactor to stimulate the single strand invasion. Expression pattern analyses showed the OsMFS1 was preferentially expressed in meiosis stage. Subcellular localization analysis of OsMFS1 revealed its association with the nucleus exclusively. In addition, a yeast two-hybrid (Y2H) and pull-down assay showed that OsMFS1 could physically interact with OsHOP2 protein to form a stable complex to ensure faithful homologous recombination. Taken together, our results indicated that OsMFS1 is indispensable to the normal development of anther and embryo sacs in rice. Frontiers Media S.A. 2020-05-15 /pmc/articles/PMC7243175/ /pubmed/32499797 http://dx.doi.org/10.3389/fpls.2020.00518 Text en Copyright © 2020 Lu, Wang, Wang, Zheng, Bai, Lei, Tian, Xiao, You, Wang, Yu, Liu, Liu, Chen, Jang, Wang, Zhao and Wan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Lu, Jiayu
Wang, Chaolong
Wang, Haiyu
Zheng, Hai
Bai, Wenting
Lei, Dekun
Tian, Yunlu
Xiao, Yanjia
You, Shimin
Wang, Qiming
Yu, Xiaowen
Liu, Shijia
Liu, Xi
Chen, Liangming
Jang, Ling
Wang, Chunming
Zhao, Zhigang
Wan, Jianmin
OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development
title OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development
title_full OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development
title_fullStr OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development
title_full_unstemmed OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development
title_short OsMFS1/OsHOP2 Complex Participates in Rice Male and Female Development
title_sort osmfs1/oshop2 complex participates in rice male and female development
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243175/
https://www.ncbi.nlm.nih.gov/pubmed/32499797
http://dx.doi.org/10.3389/fpls.2020.00518
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