Zhang‐Wei Hu, Jun‐Hua Wang, Xiao‐Yu Xiong, Hao Su, Yuan Yang, Yu‐Hui Xiao, De‐Qiang Li, Yong Zhu, Xue‐Mei Yang, Xin‐Ya Chang, He Wang, Guo‐Bang Li, Zhi‐Xue Zhao, Ji‐Wei Zhang, Yan‐Yan Huang, Jing Fan, Wen‐Ming Wang, Yan Li
{"title":"Two Transcriptional Factors Antagonistically Fine‐Tune MIR1863a to Balance Resistance and Yield Traits in Rice","authors":"Zhang‐Wei Hu, Jun‐Hua Wang, Xiao‐Yu Xiong, Hao Su, Yuan Yang, Yu‐Hui Xiao, De‐Qiang Li, Yong Zhu, Xue‐Mei Yang, Xin‐Ya Chang, He Wang, Guo‐Bang Li, Zhi‐Xue Zhao, Ji‐Wei Zhang, Yan‐Yan Huang, Jing Fan, Wen‐Ming Wang, Yan Li","doi":"10.1111/pbi.70285","DOIUrl":null,"url":null,"abstract":"Immune activation usually trades off growth, leading to yield loss. Genes that coordinate resistance and yield are urgently required for crop improvement. MicroRNAs (miRNAs) provide rich candidates for coordinating resistance with yield. Here, we demonstrated that mutation of <jats:italic>MIR1863a</jats:italic> enhances blast disease resistance without yield loss accompanying increased panicle number. However, overexpression and mutation of <jats:italic>MIR1863a</jats:italic> both lead to compromised yield traits such as seed setting rate. The expression of <jats:italic>MIR1863a</jats:italic> was antagonistically regulated by two transcription factors, MADS51 and ESR1. MADS51 activates, whereas ESR1 suppresses <jats:italic>MIR1863a</jats:italic> in leaves and panicles during the growth period and upon pathogen invasion, thus avoiding a penalty in yield caused by excessive resistance. Consistent with the phenotype of <jats:italic>mir1863a</jats:italic> lines, mutation of <jats:italic>MADS51</jats:italic> boosts blast disease resistance without yield loss. Moreover, the haplotypes of <jats:italic>MADS51</jats:italic> and <jats:italic>ESR1</jats:italic>, which exhibit differential activity on the <jats:italic>MIR1863a</jats:italic> promoter, correlate with disease phenotypes in diverse <jats:italic>Japonica</jats:italic> and <jats:italic>Indica</jats:italic> rice accessions, implying a subspecies‐specific evolution of these ‘transcriptional factor‐<jats:italic>MIR1863a</jats:italic>’ models. Taken together, our results revealed a fine‐tuning mechanism controlling an miRNA amounts to balance disease resistance and yield, advancing our understanding of the regulation of the resistance‐yield trade‐off.","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":"26 1","pages":""},"PeriodicalIF":10.5000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/pbi.70285","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Immune activation usually trades off growth, leading to yield loss. Genes that coordinate resistance and yield are urgently required for crop improvement. MicroRNAs (miRNAs) provide rich candidates for coordinating resistance with yield. Here, we demonstrated that mutation of MIR1863a enhances blast disease resistance without yield loss accompanying increased panicle number. However, overexpression and mutation of MIR1863a both lead to compromised yield traits such as seed setting rate. The expression of MIR1863a was antagonistically regulated by two transcription factors, MADS51 and ESR1. MADS51 activates, whereas ESR1 suppresses MIR1863a in leaves and panicles during the growth period and upon pathogen invasion, thus avoiding a penalty in yield caused by excessive resistance. Consistent with the phenotype of mir1863a lines, mutation of MADS51 boosts blast disease resistance without yield loss. Moreover, the haplotypes of MADS51 and ESR1, which exhibit differential activity on the MIR1863a promoter, correlate with disease phenotypes in diverse Japonica and Indica rice accessions, implying a subspecies‐specific evolution of these ‘transcriptional factor‐MIR1863a’ models. Taken together, our results revealed a fine‐tuning mechanism controlling an miRNA amounts to balance disease resistance and yield, advancing our understanding of the regulation of the resistance‐yield trade‐off.
期刊介绍:
Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.