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野生大麦抗叶斑病的关联分析

Association mapping of spot blotch resistance in wild barley.

作者信息

Roy Joy K, Smith Kevin P, Muehlbauer Gary J, Chao Shiaoman, Close Timothy J, Steffenson Brian J

出版信息

Mol Breed. 2010 Aug;26(2):243-256. doi: 10.1007/s11032-010-9402-8. Epub 2010 Mar 10.

Abstract

Spot blotch, caused by Cochliobolus sativus, is an important foliar disease of barley. The disease has been controlled for over 40 years through the deployment of cultivars with durable resistance derived from the line NDB112. Pathotypes of C. sativus with virulence for the NDB112 resistance have been detected in Canada; thus, many commercial cultivars are vulnerable to spot blotch epidemics. To increase the diversity of spot blotch resistance in cultivated barley, we evaluated 318 diverse wild barley accessions comprising the Wild Barley Diversity Collection (WBDC) for reaction to C. sativus at the seedling stage and utilized an association mapping (AM) approach to identify and map resistance loci. A high frequency of resistance was found in the WBDC as 95% (302/318) of the accessions exhibited low infection responses. The WBDC was genotyped with 558 Diversity Array Technology (DArT((R))) and 2,878 single nucleotide polymorphism (SNP) markers and subjected to structure analysis before running the AM procedure. Thirteen QTL for spot blotch resistance were identified with DArT and SNP markers. These QTL were found on chromosomes 1H, 2H, 3H, 5H, and 7H and explained from 2.3 to 3.9% of the phenotypic variance. Nearly half of the identified QTL mapped to chromosome bins where spot blotch resistance loci were previously reported, offering some validation for the AM approach. The other QTL mapped to unique genomic regions and may represent new spot blotch resistance loci. This study demonstrates that AM is an effective technique for identifying and mapping QTL for disease resistance in a wild crop progenitor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11032-010-9402-8) contains supplementary material, which is available to authorized users.

摘要

由新月弯孢菌引起的斑点病是大麦的一种重要叶部病害。在过去40多年里,通过种植具有源自NDB112品系持久抗性的品种来控制该病。在加拿大已检测到对NDB112抗性具有毒力的新月弯孢菌致病型;因此,许多商业品种易受斑点病流行的影响。为了增加栽培大麦中斑点病抗性的多样性,我们评估了318份包括野生大麦多样性收集品系(WBDC)的不同野生大麦材料在苗期对新月弯孢菌的反应,并采用关联作图(AM)方法来鉴定和定位抗性位点。在WBDC中发现了高频率的抗性,因为95%(302/318)的材料表现出低感染反应。利用558个多样性阵列技术(DArT((R)))和2878个单核苷酸多态性(SNP)标记对WBDC进行基因分型,并在运行AM程序之前进行结构分析。用DArT和SNP标记鉴定出13个斑点病抗性QTL。这些QTL位于1H、2H、3H、5H和7H染色体上,解释了2.3%至3.9%的表型变异。近一半鉴定出的QTL定位于先前报道有斑点病抗性位点的染色体区间,为AM方法提供了一些验证。其他QTL定位于独特的基因组区域,可能代表新的斑点病抗性位点。本研究表明,AM是一种在野生作物祖先中鉴定和定位抗病QTL的有效技术。电子补充材料:本文的在线版本(doi:10.1007/s11032-010-9402-8)包含补充材料,授权用户可获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac2/2908432/56840fe795e3/11032_2010_9402_Fig1_HTML.jpg

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