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利用 bulk segregant RNA 测序技术对小麦品种京紫 102 中抗白粉病基因的鉴定。

Characterization of a Powdery Mildew Resistance Gene in Wheat Breeding Line Jingzi 102 Using Bulk Segregant RNA Sequencing.

机构信息

Center for Agricultural Resources Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Shijiazhuang 050022, Hebei, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Plant Dis. 2024 Oct;108(10):3084-3091. doi: 10.1094/PDIS-02-24-0297-RE. Epub 2024 Sep 26.

Abstract

Wheat ( L.) is one of the most important crops worldwide. Powdery mildew caused by f. sp. is a destructive disease threatening wheat yield and quality. The utilization of resistant genes and cultivars is considered the most economical, environmentally friendly, and effective method to control powdery mildew. Wheat breeding line Jingzi 102 was highly resistant to powdery mildew at both seedling and adult plant stages. Genetic analysis of F, F, and F populations of "Jingzi 102 × Shixin 828" showed that the resistance of Jingzi 102 against powdery mildew isolate E09 at the seedling stage was controlled by a single dominant gene, temporarily designated . Using bulked segregant RNA sequencing combined with molecular markers analysis, was located on the long arm of chromosome 2B and flanked by markers - and - with the genetic distances of 1.2 and 0.5 centimorgan, respectively, corresponding to the bread wheat genome of Chinese Spring (International Wheat Genome Sequencing Consortium RefSeq v2.1) 703.8 to 707.6 Mb. is most likely different from the documented genes on chromosome 2BL based on their physical positions, molecular markers analysis, and resistance spectrum. Based on the gene annotation information, five genes related to disease resistance could be considered as the candidate genes of . To accelerate the application of , the flanking markers BJK695-1 and CIT02g-20 can serve for marker-assisted selection of in wheat disease-resistance breeding.

摘要

小麦(L.)是世界上最重要的作物之一。由 f. sp. 引起的白粉病是一种破坏性疾病,威胁着小麦的产量和品质。利用抗性基因和品种被认为是控制白粉病最经济、环保和有效的方法。小麦品系 Jingzi 102 在幼苗期和成株期均对白粉病表现出高度抗性。“Jingzi 102 × Shixin 828”的 F 1 、F 2 和 F 3 群体的遗传分析表明,Jingzi 102 对 E09 白粉病分离物的苗期抗性由单个显性基因控制,暂时命名为 。利用混池分离群体 RNA 测序结合分子标记分析,将 定位在 2B 染色体的长臂上,位于标记 - 和 - 之间,遗传距离分别为 1.2 和 0.5 厘摩,对应于中国春(国际小麦基因组测序联盟 RefSeq v2.1)703.8 到 707.6 Mb 的基因组。基于其物理位置、分子标记分析和抗性谱, 最有可能与染色体 2BL 上已报道的 基因不同。根据基因注释信息,可将与抗病性相关的五个基因视为 的候选基因。为了加速 的应用,侧翼标记 BJK695-1 和 CIT02g-20 可用于小麦抗病性育种中 的标记辅助选择。

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