Qiyan Liu, Dongfen Han, Denghu Cheng, Jinfan Chen, Shujuan Tian, Jiafa Wang, Man Liu, Li Yuan
{"title":"AtRKD5 可抑制 AtBBM 介导的孤雌生殖潜能。","authors":"Qiyan Liu, Dongfen Han, Denghu Cheng, Jinfan Chen, Shujuan Tian, Jiafa Wang, Man Liu, Li Yuan","doi":"10.1111/jipb.13678","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Parthenogenesis, the development of unfertilized egg cells into embryos, is a key component of apomixis. <i>AtBBM</i> (<i>BABY BOOM</i>), a crucial regulator of embryogenesis in <i>Arabidopsis</i>, possesses the capacity to shift nutritional growth toward reproductive growth. However, the mechanisms underlying <i>AtBBM</i>-induced parthenogenesis remain largely unexplored in dicot plants. Our findings revealed that in order to uphold the order of sexual reproduction, the embryo-specific promoter activity of <i>AtBBM</i> as well as repressors that inhibit its expression in egg cells combine to limiting its ability to induce parthenogenesis. Notably, AtRKD5, a RWP-RK domain-containing (RKD) transcription factor, binds to the 3′ end of <i>AtBBM</i> and is identified as one of the inhibitory factors for <i>AtBBM</i> expression in the egg cell. In the <i>atrkd5</i> mutant, we successfully achieved enhanced ectopic expression of <i>AtBBM</i> in egg cells, resulting in the generation of haploid offspring via parthenogenesis at a rate of 0.28%. Furthermore, by introducing chimeric <i>Arabidopsis</i> and rice <i>BBM</i> genes into the egg cell, we achieved a significant 4.6-fold enhancement in haploid induction through the <i>atdmp8/9</i> mutant. These findings lay a strong foundation for further exploration of the <i>BBM</i>-mediated parthenogenesis mechanism and the improvement of haploid breeding efficiency mediated by the <i>dmp8/9</i> mutant.</p></div>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":null,"pages":null},"PeriodicalIF":9.3000,"publicationDate":"2024-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"AtRKD5 inhibits the parthenogenic potential mediated by AtBBM\",\"authors\":\"Qiyan Liu, Dongfen Han, Denghu Cheng, Jinfan Chen, Shujuan Tian, Jiafa Wang, Man Liu, Li Yuan\",\"doi\":\"10.1111/jipb.13678\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Parthenogenesis, the development of unfertilized egg cells into embryos, is a key component of apomixis. <i>AtBBM</i> (<i>BABY BOOM</i>), a crucial regulator of embryogenesis in <i>Arabidopsis</i>, possesses the capacity to shift nutritional growth toward reproductive growth. However, the mechanisms underlying <i>AtBBM</i>-induced parthenogenesis remain largely unexplored in dicot plants. Our findings revealed that in order to uphold the order of sexual reproduction, the embryo-specific promoter activity of <i>AtBBM</i> as well as repressors that inhibit its expression in egg cells combine to limiting its ability to induce parthenogenesis. Notably, AtRKD5, a RWP-RK domain-containing (RKD) transcription factor, binds to the 3′ end of <i>AtBBM</i> and is identified as one of the inhibitory factors for <i>AtBBM</i> expression in the egg cell. In the <i>atrkd5</i> mutant, we successfully achieved enhanced ectopic expression of <i>AtBBM</i> in egg cells, resulting in the generation of haploid offspring via parthenogenesis at a rate of 0.28%. Furthermore, by introducing chimeric <i>Arabidopsis</i> and rice <i>BBM</i> genes into the egg cell, we achieved a significant 4.6-fold enhancement in haploid induction through the <i>atdmp8/9</i> mutant. These findings lay a strong foundation for further exploration of the <i>BBM</i>-mediated parthenogenesis mechanism and the improvement of haploid breeding efficiency mediated by the <i>dmp8/9</i> mutant.</p></div>\",\"PeriodicalId\":195,\"journal\":{\"name\":\"Journal of Integrative Plant Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":9.3000,\"publicationDate\":\"2024-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Integrative Plant Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/jipb.13678\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Integrative Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jipb.13678","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
AtRKD5 inhibits the parthenogenic potential mediated by AtBBM
Parthenogenesis, the development of unfertilized egg cells into embryos, is a key component of apomixis. AtBBM (BABY BOOM), a crucial regulator of embryogenesis in Arabidopsis, possesses the capacity to shift nutritional growth toward reproductive growth. However, the mechanisms underlying AtBBM-induced parthenogenesis remain largely unexplored in dicot plants. Our findings revealed that in order to uphold the order of sexual reproduction, the embryo-specific promoter activity of AtBBM as well as repressors that inhibit its expression in egg cells combine to limiting its ability to induce parthenogenesis. Notably, AtRKD5, a RWP-RK domain-containing (RKD) transcription factor, binds to the 3′ end of AtBBM and is identified as one of the inhibitory factors for AtBBM expression in the egg cell. In the atrkd5 mutant, we successfully achieved enhanced ectopic expression of AtBBM in egg cells, resulting in the generation of haploid offspring via parthenogenesis at a rate of 0.28%. Furthermore, by introducing chimeric Arabidopsis and rice BBM genes into the egg cell, we achieved a significant 4.6-fold enhancement in haploid induction through the atdmp8/9 mutant. These findings lay a strong foundation for further exploration of the BBM-mediated parthenogenesis mechanism and the improvement of haploid breeding efficiency mediated by the dmp8/9 mutant.
期刊介绍:
Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.