Brems1突变诱导绦膜缺失导致大白菜雄性不育。

IF 4.4 1区 农林科学 Q1 AGRONOMY Theoretical and Applied Genetics Pub Date : 2025-02-24 DOI:10.1007/s00122-025-04841-y
Chuanhong Liu, Lin Wang, Chong Tan, Di Zhao, Zhiyong Liu
{"title":"Brems1突变诱导绦膜缺失导致大白菜雄性不育。","authors":"Chuanhong Liu, Lin Wang, Chong Tan, Di Zhao, Zhiyong Liu","doi":"10.1007/s00122-025-04841-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Key message: </strong>The mutation in Brems1 resulting in male sterility in Chinese cabbage were validated through two allelic mutations. Male sterile lines are ideal for hybrid seed production in Chinese cabbage. Herein, the complete male sterile mutants M5026 and M5073 were obtained through ethyl methanesulfonate (EMS) mutagenesis in the Chinese cabbage double haploid line 'FT'. Cytological observations revealed that M5026 exhibited an absence of the tapetum, an overabundance of microsporocytes, and abnormal exine formation in pollen. The male sterility phenotype of M5026 was controlled by a single recessive nuclear gene. Using mutmap sequencing and kompetitive allele-specific PCR (KASP) identification and gene cloning, two distinct SNPs in BraA10g029920.3.5C, encoding EMS1 (excess microsporocytes 1), were identified to be associated with the male sterility of M5026 and M5073. The gene was named as Brems1. M5026 and M5073 were determined to be allelic variants. Both BrEMS1 and Brems1 were subcellularly localized at the cell membrane. Brems1 exhibited the highest expression level in buds, while no expression was detected in roots. Transcriptomic analysis revealed that Brems1 mutations reduced the expression levels of genes associated with the tapetum, pollen tube, and LRR-RLK family. These results suggested that Brems1 played a critical role in pollen development and contributes to elucidating the molecular mechanisms underlying tapetum development and male sterility in Chinese cabbage.</p>","PeriodicalId":22955,"journal":{"name":"Theoretical and Applied Genetics","volume":"138 3","pages":"50"},"PeriodicalIF":4.4000,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Brems1 mutation induced tapetum deficiency leading to male sterility in Chinese cabbage (Brassica rapa L. ssp. pekinensis).\",\"authors\":\"Chuanhong Liu, Lin Wang, Chong Tan, Di Zhao, Zhiyong Liu\",\"doi\":\"10.1007/s00122-025-04841-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Key message: </strong>The mutation in Brems1 resulting in male sterility in Chinese cabbage were validated through two allelic mutations. Male sterile lines are ideal for hybrid seed production in Chinese cabbage. Herein, the complete male sterile mutants M5026 and M5073 were obtained through ethyl methanesulfonate (EMS) mutagenesis in the Chinese cabbage double haploid line 'FT'. Cytological observations revealed that M5026 exhibited an absence of the tapetum, an overabundance of microsporocytes, and abnormal exine formation in pollen. The male sterility phenotype of M5026 was controlled by a single recessive nuclear gene. Using mutmap sequencing and kompetitive allele-specific PCR (KASP) identification and gene cloning, two distinct SNPs in BraA10g029920.3.5C, encoding EMS1 (excess microsporocytes 1), were identified to be associated with the male sterility of M5026 and M5073. The gene was named as Brems1. M5026 and M5073 were determined to be allelic variants. Both BrEMS1 and Brems1 were subcellularly localized at the cell membrane. Brems1 exhibited the highest expression level in buds, while no expression was detected in roots. Transcriptomic analysis revealed that Brems1 mutations reduced the expression levels of genes associated with the tapetum, pollen tube, and LRR-RLK family. These results suggested that Brems1 played a critical role in pollen development and contributes to elucidating the molecular mechanisms underlying tapetum development and male sterility in Chinese cabbage.</p>\",\"PeriodicalId\":22955,\"journal\":{\"name\":\"Theoretical and Applied Genetics\",\"volume\":\"138 3\",\"pages\":\"50\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-02-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Theoretical and Applied Genetics\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1007/s00122-025-04841-y\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRONOMY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Theoretical and Applied Genetics","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s00122-025-04841-y","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRONOMY","Score":null,"Total":0}
引用次数: 0
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Brems1 mutation induced tapetum deficiency leading to male sterility in Chinese cabbage (Brassica rapa L. ssp. pekinensis).

Key message: The mutation in Brems1 resulting in male sterility in Chinese cabbage were validated through two allelic mutations. Male sterile lines are ideal for hybrid seed production in Chinese cabbage. Herein, the complete male sterile mutants M5026 and M5073 were obtained through ethyl methanesulfonate (EMS) mutagenesis in the Chinese cabbage double haploid line 'FT'. Cytological observations revealed that M5026 exhibited an absence of the tapetum, an overabundance of microsporocytes, and abnormal exine formation in pollen. The male sterility phenotype of M5026 was controlled by a single recessive nuclear gene. Using mutmap sequencing and kompetitive allele-specific PCR (KASP) identification and gene cloning, two distinct SNPs in BraA10g029920.3.5C, encoding EMS1 (excess microsporocytes 1), were identified to be associated with the male sterility of M5026 and M5073. The gene was named as Brems1. M5026 and M5073 were determined to be allelic variants. Both BrEMS1 and Brems1 were subcellularly localized at the cell membrane. Brems1 exhibited the highest expression level in buds, while no expression was detected in roots. Transcriptomic analysis revealed that Brems1 mutations reduced the expression levels of genes associated with the tapetum, pollen tube, and LRR-RLK family. These results suggested that Brems1 played a critical role in pollen development and contributes to elucidating the molecular mechanisms underlying tapetum development and male sterility in Chinese cabbage.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
9.60
自引率
7.40%
发文量
241
审稿时长
2.3 months
期刊介绍: Theoretical and Applied Genetics publishes original research and review articles in all key areas of modern plant genetics, plant genomics and plant biotechnology. All work needs to have a clear genetic component and significant impact on plant breeding. Theoretical considerations are only accepted in combination with new experimental data and/or if they indicate a relevant application in plant genetics or breeding. Emphasizing the practical, the journal focuses on research into leading crop plants and articles presenting innovative approaches.
期刊最新文献
Fine mapping of the unique Ur-11 gene conferring broad resistance to the rust pathogen of common bean. Fine mapping of stripe rust resistance gene YrAn1589 in common wheat using Wheat660K SNP array and BSR-Seq. Optimization of sparse phenotyping strategy in multi-environmental trials in maize. The knockout of Gγ subunit HvGS3 by CRISPR/Cas9 gene editing improves the lodging resistance of barley through dwarfing and stem strengthening. Characterization of a stable QTL for quality-related traits and its effects on yields in wheat (Triticum aestivum L.).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1