A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus

The Ogura cytoplasmic male sterility (CMS) line of Brassica napus has gained significant attention for its use in harnessing heterosis. It remains unaffected by temperature and environment and is thorough and stable. The Ogura cytoplasmic restorer line of Brassica napus is derived from the distant h...

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Main Authors: Xuesong Wang, Xingyu Liang, Rui Wang, Yuan Gao, Yun Li, Haoran Shi, Wanzhuo Gong, Saira Saleem, Qiong Zou, Lanrong Tao, Zeming Kang, Jin Yang, Qin Yu, Qiaobo Wu, Hailan Liu, Shaohong Fu
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Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Genetics
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Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2024.1521277/full
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author Xuesong Wang
Xingyu Liang
Rui Wang
Yuan Gao
Yun Li
Haoran Shi
Wanzhuo Gong
Saira Saleem
Qiong Zou
Lanrong Tao
Zeming Kang
Jin Yang
Qin Yu
Qiaobo Wu
Hailan Liu
Shaohong Fu
author_facet Xuesong Wang
Xingyu Liang
Rui Wang
Yuan Gao
Yun Li
Haoran Shi
Wanzhuo Gong
Saira Saleem
Qiong Zou
Lanrong Tao
Zeming Kang
Jin Yang
Qin Yu
Qiaobo Wu
Hailan Liu
Shaohong Fu
author_sort Xuesong Wang
collection DOAJ
description The Ogura cytoplasmic male sterility (CMS) line of Brassica napus has gained significant attention for its use in harnessing heterosis. It remains unaffected by temperature and environment and is thorough and stable. The Ogura cytoplasmic restorer line of Brassica napus is derived from the distant hybridization of Raphanus sativus L. and B. napus, but it carried a large number of radish fragments into Brassica napus, because there is no homologous allele of the restorer gene in B. napus, transferring it becomes challenging. In this study, the double haploid induction line in B. napus was used as the male parent for hybridization with the Ogura CMS of B. napus. Surprisingly, fertile plants appeared in the offspring. Further analysis revealed that the cytoplasmic type, ploidy, and chromosome number of the fertile offspring were consistent with the sterile female parent. Moreover, the mitochondrial genome similarity between the fertile offspring and the sterile female parent was 97.7% indicates that the cytoplasm of the two is the same, while the nuclear gene difference between fertile offspring and sterile female parent was only 10.33%, indicates that new genes appeared in the offspring. To further investigate and locate the restorer gene, the BSA method was employed to construct extreme mixed pools. As a result, the restorer gene was mapped to three positions: A09 chromosome 10.99–17.20 Mb, C03 chromosome 5.07–5.34 Mb, and C09 chromosome 18.78–36.60 Mb. The experimental results have proved that induction does produce restorer genes. The induction of the Ogura CMS restorer gene through DH induction line provides a promising new approach for harnessing heterosis in B. napus.
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spelling doaj-art-e25a117453e24da9b6dcf30d86620e8f2025-01-06T06:59:01ZengFrontiers Media S.A.Frontiers in Genetics1664-80212025-01-011510.3389/fgene.2024.15212771521277A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napusXuesong Wang0Xingyu Liang1Rui Wang2Yuan Gao3Yun Li4Haoran Shi5Wanzhuo Gong6Saira Saleem7Qiong Zou8Lanrong Tao9Zeming Kang10Jin Yang11Qin Yu12Qiaobo Wu13Hailan Liu14Shaohong Fu15Maize Research Institute of Sichuan Agricultural University, Chengdu, ChinaMaize Research Institute of Sichuan Agricultural University, Chengdu, ChinaMaize Research Institute of Sichuan Agricultural University, Chengdu, ChinaMaize Research Institute of Sichuan Agricultural University, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaOilseeds Research Station, Khanpur, Ayub Agricultural Research Institute, Faisalabad, PakistanNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaMaize Research Institute of Sichuan Agricultural University, Chengdu, ChinaNational Rapeseed Genetic Improvement Center, Chengdu Academy of Agriculture and Forestry Sciences, Chengdu Research Branch, Chengdu, ChinaThe Ogura cytoplasmic male sterility (CMS) line of Brassica napus has gained significant attention for its use in harnessing heterosis. It remains unaffected by temperature and environment and is thorough and stable. The Ogura cytoplasmic restorer line of Brassica napus is derived from the distant hybridization of Raphanus sativus L. and B. napus, but it carried a large number of radish fragments into Brassica napus, because there is no homologous allele of the restorer gene in B. napus, transferring it becomes challenging. In this study, the double haploid induction line in B. napus was used as the male parent for hybridization with the Ogura CMS of B. napus. Surprisingly, fertile plants appeared in the offspring. Further analysis revealed that the cytoplasmic type, ploidy, and chromosome number of the fertile offspring were consistent with the sterile female parent. Moreover, the mitochondrial genome similarity between the fertile offspring and the sterile female parent was 97.7% indicates that the cytoplasm of the two is the same, while the nuclear gene difference between fertile offspring and sterile female parent was only 10.33%, indicates that new genes appeared in the offspring. To further investigate and locate the restorer gene, the BSA method was employed to construct extreme mixed pools. As a result, the restorer gene was mapped to three positions: A09 chromosome 10.99–17.20 Mb, C03 chromosome 5.07–5.34 Mb, and C09 chromosome 18.78–36.60 Mb. The experimental results have proved that induction does produce restorer genes. The induction of the Ogura CMS restorer gene through DH induction line provides a promising new approach for harnessing heterosis in B. napus.https://www.frontiersin.org/articles/10.3389/fgene.2024.1521277/fullBrassica napusdouble haploid (DH) inducerOgura cytoplasmic male sterilityrestorer geneBSAmolecular marker
spellingShingle Xuesong Wang
Xingyu Liang
Rui Wang
Yuan Gao
Yun Li
Haoran Shi
Wanzhuo Gong
Saira Saleem
Qiong Zou
Lanrong Tao
Zeming Kang
Jin Yang
Qin Yu
Qiaobo Wu
Hailan Liu
Shaohong Fu
A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus
Frontiers in Genetics
Brassica napus
double haploid (DH) inducer
Ogura cytoplasmic male sterility
restorer gene
BSA
molecular marker
title A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus
title_full A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus
title_fullStr A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus
title_full_unstemmed A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus
title_short A breeding method for Ogura CMS restorer line independent of restorer source in Brassica napus
title_sort breeding method for ogura cms restorer line independent of restorer source in brassica napus
topic Brassica napus
double haploid (DH) inducer
Ogura cytoplasmic male sterility
restorer gene
BSA
molecular marker
url https://www.frontiersin.org/articles/10.3389/fgene.2024.1521277/full
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