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An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids
Hybrid sterility (HS) between Oryza sativa (Asian rice) and O. glaberrima (African rice) is mainly controlled by the S1 locus. However, our limited understanding of the HS mechanism hampers utilization of the strong interspecific heterosis. Here, we show that three closely linked genes (S1A4, S1TPR,...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555797/ https://www.ncbi.nlm.nih.gov/pubmed/31175302 http://dx.doi.org/10.1038/s41467-019-10488-3 |
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author | Xie, Yongyao Tang, Jintao Xie, Xianrong Li, Xiaojuan Huang, Jianle Fei, Yue Han, Jingluan Chen, Shuifu Tang, Huiwu Zhao, Xiucai Tao, Dayun Xu, Peng Liu, Yao-Guang Chen, Letian |
author_facet | Xie, Yongyao Tang, Jintao Xie, Xianrong Li, Xiaojuan Huang, Jianle Fei, Yue Han, Jingluan Chen, Shuifu Tang, Huiwu Zhao, Xiucai Tao, Dayun Xu, Peng Liu, Yao-Guang Chen, Letian |
author_sort | Xie, Yongyao |
collection | PubMed |
description | Hybrid sterility (HS) between Oryza sativa (Asian rice) and O. glaberrima (African rice) is mainly controlled by the S1 locus. However, our limited understanding of the HS mechanism hampers utilization of the strong interspecific heterosis. Here, we show that three closely linked genes (S1A4, S1TPR, and S1A6) in the African S1 allele (S1-g) constitute a killer-protector system that eliminates gametes carrying the Asian allele (S1-s). In Asian–African rice hybrids (S1-gS1-s), the S1TPR-S1A4-S1A6 interaction in sporophytic tissues generates an abortion signal to male and female gametes. However, S1TPR can rescue S1-g gametes, while the S1-s gametes selectively abort for lacking S1TPR. Knockout of any of the S1-g genes eliminates the HS. Evolutionary analysis suggests that S1 may have arisen from newly evolved genes, multi-step recombination, and nucleotide variations. Our findings will help to overcome the interspecific reproductive barrier and use Asian–African hybrids for increasing rice production. |
format | Online Article Text |
id | pubmed-6555797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65557972019-06-21 An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids Xie, Yongyao Tang, Jintao Xie, Xianrong Li, Xiaojuan Huang, Jianle Fei, Yue Han, Jingluan Chen, Shuifu Tang, Huiwu Zhao, Xiucai Tao, Dayun Xu, Peng Liu, Yao-Guang Chen, Letian Nat Commun Article Hybrid sterility (HS) between Oryza sativa (Asian rice) and O. glaberrima (African rice) is mainly controlled by the S1 locus. However, our limited understanding of the HS mechanism hampers utilization of the strong interspecific heterosis. Here, we show that three closely linked genes (S1A4, S1TPR, and S1A6) in the African S1 allele (S1-g) constitute a killer-protector system that eliminates gametes carrying the Asian allele (S1-s). In Asian–African rice hybrids (S1-gS1-s), the S1TPR-S1A4-S1A6 interaction in sporophytic tissues generates an abortion signal to male and female gametes. However, S1TPR can rescue S1-g gametes, while the S1-s gametes selectively abort for lacking S1TPR. Knockout of any of the S1-g genes eliminates the HS. Evolutionary analysis suggests that S1 may have arisen from newly evolved genes, multi-step recombination, and nucleotide variations. Our findings will help to overcome the interspecific reproductive barrier and use Asian–African hybrids for increasing rice production. Nature Publishing Group UK 2019-06-07 /pmc/articles/PMC6555797/ /pubmed/31175302 http://dx.doi.org/10.1038/s41467-019-10488-3 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Xie, Yongyao Tang, Jintao Xie, Xianrong Li, Xiaojuan Huang, Jianle Fei, Yue Han, Jingluan Chen, Shuifu Tang, Huiwu Zhao, Xiucai Tao, Dayun Xu, Peng Liu, Yao-Guang Chen, Letian An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
title | An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
title_full | An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
title_fullStr | An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
title_full_unstemmed | An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
title_short | An asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
title_sort | asymmetric allelic interaction drives allele transmission bias in interspecific rice hybrids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555797/ https://www.ncbi.nlm.nih.gov/pubmed/31175302 http://dx.doi.org/10.1038/s41467-019-10488-3 |
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