{"title":"Comprehensive analysis of Brassica napus Glycosyl hydrolase family 1 genes and functional analysis of BnaBGLU27.C08 in clubroot resistance.","authors":"Yiji Shi, Xiang Liu, Shunjun Bao, Ye Li, Yuqing Shi, Chen Liang, Hongyu Sha, Zihao Yu, Qing Su, Xiyu Zhang, Xiaoyan Li, Weinan Sun, Chengyu Yu, Keqi Li, Zhen Huang","doi":"10.1186/s12864-025-11638-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>β-Glycosidases (BGLUs), belonging to the Glycoside Hydrolase Family 1 (GH1), play crucial roles in plant growth, development, and stress adaptation. While BGLUs have been extensively characterized in various plants, a comprehensive analysis of the BGLU family in Brassica napus has yet to be conducted.</p><p><strong>Results: </strong>In this study, we identified 131 BnaBGLU genes in B. napus and classified them into 11 subfamilies. Gene duplication analysis revealed that the expansion of the BnaBGLU family primarily resulted from segmental duplications. Structural analysis revealed high conservation within subfamilies, while promoter cis-element profiling and transcriptional studies under phytohormone treatments and abiotic stresses demonstrated BnaBGLUs respond to diverse environmental stimuli. Additionally, BnaBGLUs exhibit tissue-specific expression patterns. Notably, BnaBGLU27.C08 was significantly upregulated 96 h post-inoculation with Plasmodiophora brassicae in the root of clubroot-resistant (CR) B. napus varieties. Furthermore, overexpression of BnaBGLU27.C08 in Arabidopsis significantly enhanced resistance to clubroot disease.</p><p><strong>Conclusions: </strong>These findings establish a foundation for further investigation on the BnaBGLU family in B. napus and offer potential candidate genes for breeding CR B. napus varieties.</p>","PeriodicalId":9030,"journal":{"name":"BMC Genomics","volume":"26 1","pages":"515"},"PeriodicalIF":3.5000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12093868/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12864-025-11638-2","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: β-Glycosidases (BGLUs), belonging to the Glycoside Hydrolase Family 1 (GH1), play crucial roles in plant growth, development, and stress adaptation. While BGLUs have been extensively characterized in various plants, a comprehensive analysis of the BGLU family in Brassica napus has yet to be conducted.
Results: In this study, we identified 131 BnaBGLU genes in B. napus and classified them into 11 subfamilies. Gene duplication analysis revealed that the expansion of the BnaBGLU family primarily resulted from segmental duplications. Structural analysis revealed high conservation within subfamilies, while promoter cis-element profiling and transcriptional studies under phytohormone treatments and abiotic stresses demonstrated BnaBGLUs respond to diverse environmental stimuli. Additionally, BnaBGLUs exhibit tissue-specific expression patterns. Notably, BnaBGLU27.C08 was significantly upregulated 96 h post-inoculation with Plasmodiophora brassicae in the root of clubroot-resistant (CR) B. napus varieties. Furthermore, overexpression of BnaBGLU27.C08 in Arabidopsis significantly enhanced resistance to clubroot disease.
Conclusions: These findings establish a foundation for further investigation on the BnaBGLU family in B. napus and offer potential candidate genes for breeding CR B. napus varieties.
期刊介绍:
BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics.
BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.