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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,...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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