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首页> 外文期刊>Euphytica >Development of molecular markers linked to the Fom-1 locus for resistance to Fusarium race 2 in melon
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Development of molecular markers linked to the Fom-1 locus for resistance to Fusarium race 2 in melon

机译:与Fom-1基因座相关的分子标记的开发,该标记对瓜类中的镰孢2号具有抗性

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摘要

Fusarium wilt, caused by Fusarium oxysporum f. sp. melonis (F.o.m), is a worldwide soil-borne disease of melon (Cucumis melo L.). The most effective control measure available is the use of resistant varieties. Resistance to races 0 and 2 of this fungal pathogen is conditioned by the dominant gene Fom-1. An F2 population derived from the ‘Charentais-Fom1’ × ‘TRG-1551’ cross was used in combination with bulked segregant analysis utilizing the random amplified polymorphic DNA (RAPD) markers, in order to develop molecular markers linked to the locus Fom-1. Four hundred decamer primers were screened to identify three RAPD markers (B17649, V01578, and V061092) linked to Fom-1 locus. Fragments amplified by primers B17649 and V01578 were linked in coupling phase to Fom1, at 3.5 and 4 cM respectively, whereas V061092 marker was linked in repulsion to the same dominant resistant allele at 15.1 cM from the Fom-1 locus. These RAPDs were cloned and sequenced in order to design primers that would amplify only the target fragment. The derived sequence characterized amplified region (SCAR) markers SB17645 and SV01574 (645 and 574 bp, respectively) were present only in the resistant parent. The SV061092 marker amplified a band of 1092 bp only in the susceptible parent. These markers are more universal than the CAPS markers developed by Brotman et al. (Theor Appl Genet 10:337–345, 2005). The analysis of 24 melon accessions, representing several melon types, with these markers revealed that different melon types behaved differently with the developed markers supporting the theory of multiple, independent origins of resistance to races 0 and 2 of F.o.m.
机译:枯萎病引起的枯萎病f。 sp。哈密​​瓜(F.o.m)是世界范围内由土壤传播的哈密瓜(Cucumis melo L.)疾病。可用的最有效的控制措施是使用抗性品种。对这种真菌病原体的第0和第2种种族的抗性由显性基因Fom-1决定。为了研究分子的分子结构,使用了源自'Charentais-Fom1'×'TRG-1551'杂交的F 2 种群,并与利用大量扩增的segregant分析相结合,利用随机扩增多态DNA(RAPD)标记与基因座Fom-1相关的标记。筛选了400个decamer引物,以鉴定与Fom-1基因座相关的三个RAPD标记(B17 649 ,V01 578 和V06 1092 )。用引物B17 649 和V01 578 扩增的片段在偶联阶段分别以3.5和4 cM与Fom1连接,而V06 1092 标记是与Fom-1基因座的15.1 cM排斥力相同的显性抗性等位基因连锁。克隆并测序这些RAPD,以设计仅扩增靶标片段的引物。衍生的特征序列扩增区(SCAR)标记SB17 645 和SV01 574 (分别为645和574 bp)仅存在于抗性亲本中。 SV06 1092 标记仅在易感亲本中扩增了1092 bp的条带。这些标记比Brotman等人开发的CAPS标记更通用。 (Theor Appl Genet 10:337–345,2005)。用这些标记对代表几种甜瓜类型的24种甜瓜种质的分析表明,不同的甜瓜类型表现出不同的行为,与发达的标记支持F.o.m的第0和第2种抗性的多个独立起源理论有关。

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