玉米类病斑突变体Lmm18的表型与初定位分析  

Phenotypic Analysis and Initial Gene Mapping of the Maize Lesion Mimic Mutant Lmm18

作　　者：马文豪 王盈 葛启栋 陈梦瑶 李见坤 苟明月 MA Wen-hao;WANG Ying;GE Qi-dong;CHEN Meng-yao;LI Jian-kun;GOU Ming-yue(College of Agriculture,Henan Agricultural University/Co-construction State Key Laboratory of Wheat and Maize Crop Science,Zhengzhou 450002,China)

机构地区：[1]河南农业大学农学院/省部共建小麦玉米国家重点实验室,郑州450002

出　　处：《玉米科学》2024年第3期26-31,41,共7页Journal of Maize Sciences

基　　金：河南省杰出青年科学基金项目(212300410007);NSFC-河南联合基金项目(U2004207);河南省“中原千人计划”中原青年拔尖人才项目(ZYQR201912168);2022年度省级科技研发计划联合基金项目(应用攻关类)(222103810003)。

摘　　要：发掘玉米抗病种质资源,克隆抗病基因并解析玉米抗病机制,是玉米抗病性品种改良的基础。类病斑突变体(Lesion mimic mutant,Lmm)是一类在没有病原菌侵染或其他外界刺激情况下,表现出类似病害所致自发性坏死斑的突变体,是研究植物抗病机制的重要材料。对类病斑突变体Lmm18进行表型鉴定和基因初定位。该突变体首先在叶尖部表现类病斑坏死表型,坏死斑随着生长沿叶脉逐渐扩展增多,最后遍及整个叶片。通过二氨基联苯胺(3,3’-diaminobenzidine,DAB)染色,发现Lmm18中过氧化氢含量相较于野生型明显增多。此外,抗病标志基因PATHOGENESIS-RELATED 1(PR1)和PR5在Lmm18中显著上调,表明该突变体启动了抗病防御反应。遗传分析表明,该性状由显性单基因控制。利用B73与Lmm18杂交构建的F_(2)群体进行BSR-Seq(Bulked Segregant RNA-Sequencing)分析及连锁标记定位,将LMM18基因初步定位到2号染色体1.23 Mb的区间内,该研究为后续克隆该基因并解析其介导的抗病防御调控机制奠定了基础。Identifying the disease resistant maize germplasm,cloning of the casual genes as well as dissecting the associated mechanism are the basis for molecular improvement to obtain disease-resistant maize varieties.Lesion mimic mutants(Lmm/lmm)are a series of mutants that display disease-like spontaneous lesions in the absence of pathogen infection and other stimulus.In this study,phenotypic identification and initial gene mapping of the Lmml8 mutant were conducted.Small necrotic lesions were initially visible on the tips of the leaves then expand along with veins to the whole leaves eventually.Hydrogen peroxide accumulation was found increased dramatically in Lmm18 compared to the wild type by DAB(3,3'-diaminobenzidine)staining.Additionally,disease resistance marker genes PATHOGENESIS-RELATED 1(PRI)and PR5 were also significantly up-regulated in Lmm18,indicating activated defense response.Further genetic analysis showed that Lmml8 was controlled by a single dominant gene.BSR-Seq analysis was performed using the F2 population generated by cross between B73 and Lmm18.The causal gene has been initially mapped to the region of 1.23 Mb on chromosome 2,which is the basis for subsequent gene cloning and dissection of LMM18-mediated defense regulation.

关 键 词：玉米 类病斑突变体 抗病防御反应 BSR-seq 基因定位 

分 类 号：S513.035.3[农业科学—作物学]