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大豆中**(此处原文缺失相关基因名称)**启动子和编码区的突变导致**(此处原文缺失相关病原体名称)**对大豆的毒力增强。

Mutations in the Promoter and Coding Regions of Cause Gain of Virulence of to in Soybean.

作者信息

Hu Yanhong, He Zhihua, Kang Yebin, Cui Linkai

机构信息

College of Horticulture and Plant Protection, Henan University of Science and Technology, Luoyang, China.

出版信息

Front Microbiol. 2021 Nov 11;12:759196. doi: 10.3389/fmicb.2021.759196. eCollection 2021.

Abstract

threatens soybean production worldwide, and the cultivation of soybean cultivars carrying genes is the most effective way to control this pathogen. However, DNA mutations in the genes of can escape recognization of the corresponding genes, leading to the loss of soybean resistance. In this study, we investigated sequence polymorphism and transcript level of the gene in Chinese isolates of . Twenty-four mutations resulting in five unique alleles were discovered in the coding region from 32 isolates. The transcripts were detectable in the isolates containing (I), (II), (III), and (IV) but not in the isolates containing (V). Promoter and 5'-UTR sequence analysis revealed eight unique mutations in the promoter region of (V), suggesting that the mutations could result in the loss of (V) transcription. Virulence tests indicated the isolates containing (II) and (IV) were virulent, suggesting that the mutations in the coding regions of (II) and (IV) caused the gain of virulence to . Based on DNA mutations of in virulent alleles, two SNP markers and one PCR-based marker were developed successfully for detecting the virulence of isolates to . These findings provide new insights into escape mechanisms of and effective support for accurate pathotype identification of using molecular methods.

摘要

大豆疫霉威胁着全球大豆生产,培育携带抗性基因的大豆品种是控制这种病原菌的最有效方法。然而,大豆疫霉抗性基因中的DNA突变可逃避相应抗性基因的识别,导致大豆抗性丧失。在本研究中,我们调查了中国大豆疫霉菌株中抗性基因的序列多态性和转录水平。在32个大豆疫霉菌株的抗性基因编码区发现了导致5个独特抗性等位基因的24个突变。在含有(I)、(II)、(III)和(IV)的菌株中可检测到抗性转录本,而在含有(V)的菌株中未检测到。启动子和5'-UTR序列分析揭示了(V)启动子区域的8个独特突变,表明这些突变可能导致(V)转录丧失。致病性测试表明,含有(II)和(IV)的菌株具有致病性,这表明(II)和(IV)编码区的突变导致了对大豆疫霉的致病性增强。基于毒性等位基因中大豆疫霉的DNA突变,成功开发了两个SNP标记和一个基于PCR的标记,用于检测大豆疫霉菌株对大豆疫霉的毒性。这些发现为大豆疫霉的逃逸机制提供了新的见解,并为利用分子方法准确鉴定大豆疫霉致病型提供了有效支持。

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