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Identification of two AFLP markers linked to bacterial wilt resistance in tomato and conversion to SCAR markers

机译:鉴定两个与番茄的青枯病抗性相关的AFLP标记并转化为SCAR标记

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摘要

Tomato bacterial wilt (BW) incited by Ralstonia solanacearum is a constraint on tomato production in tropical, subtropical and humid regions of the world. In this paper, we present the results of a research aimed at the identification of PCR-based markers amplified fragment length polymorphism (AFLP) linked to the genes that confer resistance to tomato BW. To this purpose, bulked segregant analysis was applied to an F(2) population segregating for the BW resistant gene and derived from the pair-cross between a BW resistant cultivar T51A and the susceptible cultivar T9230. Genetic analysis indicated that tomato BW was conferred by two incomplete dominant genes. A CTAB method for total DNA extraction, developed by Murray and Thompson with some modifications was used to isolation the infected tomato leaves. Thirteen differential fragments were detected using 256 primer combinations, and two AFLP markers were linked to the BW resistance. Subsequently, the AFLP markers were converted to co-dominant SCAR markers, named TSCAR(AAT/CGA) and TSCAR(AAG/CAT). Linkage analysis showed that the two markers are on the contralateral side of TRSR-1. Genetic distance between TSCAR(AAT/CGA) and TRS-1 was estimated to 4.6 cM, while 8.4 cM between TSCAR(AAG/CAT) and TRS-1.
机译:Ralstonia solanacearum引起的番茄枯萎病是世界热带,亚热带和湿润地区番茄产量的制约因素。在本文中,我们提出了一项旨在鉴定基于PCR的标记的扩增片段长度多态性(AFLP)的研究结果,该片段与赋予番茄BW抗性的基因相关。为此,将大量隔离剂分析应用于针对BW抗性基因分离的F(2)种群,并从BW抗性品种T51A与易感品种T9230之间的成对杂交获得。遗传分析表明,番茄BW由两个不完全的显性基因赋予。由Murray和Thompson开发并经过一些修改的CTAB总DNA提取方法用于分离感染的番茄叶片。使用256个引物组合检测到13个差异片段,并将两个AFLP标记与BW抗性相关。随后,将AFLP标记转换为共占主导的SCAR标记,分别称为TSCAR(AAT / CGA)和TSCAR(AAG / CAT)。连锁分析表明,这两个标记位于TRSR-1的对侧。 TSCAR(AAT / CGA)与TRS-1之间的遗传距离估计为4.6 cM,而TSCAR(AAG / CAT)与TRS-1之间的遗传距离为8.4 cM。

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