首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Fine mapping of pepper trichome locus 1 controlling trichome formation in Capsicum annuum L. CM334
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Fine mapping of pepper trichome locus 1 controlling trichome formation in Capsicum annuum L. CM334

机译:辣椒毛状体基因座1的精细定位,可控制辣椒辣椒中毛状体的形成.CM334

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摘要

Trichomes are present on nearly all land plants and protect plants against insect herbivores, drought and UV radiation. The trichome-bearing phenotype is conferred by the dominant allele of the pepper trichome locus 1 (Ptl1) in Capsicum annuum, Mexican Criollo de Morelos-334' (CM334). A genetic analysis using simple sequence repeats from pepper cDNA identified the HpmsE031 marker as tightly linked to Ptl1 in 653 individuals of an F population derived from a cross between CM334 and Chilsungcho varieties. A bacterial artificial chromosome (BAC) library from CM334 covering 12c of the genome was screened using the HpmsE031 SSR marker as a probe and three BAC clones were identified. The Ptl1 region was covered by one 80 kb BAC clone, TT1B7. Fluorescence in situ hybridization (FISH) confirmed that TT1B7 localized to pepper chromosome 10. One co-dominant marker, Tco, and one dominant marker, Tsca, were successfully developed from the TT1B7 BAC sequence. Tco mapped 0.33 cM up from Ptl1 and Tsca mapped 0.75 cM down from Ptl1. Analysis of the BAC sequence predicts the presence of 14 open reading frames including 60S ribosomal protein L21-like protein (Solanum demissum), protein kinase 2 (Nicotiana tabacum), hypothetical proteins, and unnamed protein products. These results will provide not only useful information for map-based cloning of Ptl1 in Capsicum but also the starting points for analysis of R-gene cluster inked with Ptl1.
机译:滴虫几乎存在于所有陆地植物上,并保护植物免受昆虫食草动物,干旱和紫外线的伤害。毛状体表型是由辣椒的毛状体毛状体基因座1(Ptl1)的优势等位基因赋予的,其位于墨西哥辣椒的Criolo de Morelos-334'(CM334)中。使用来自辣椒cDNA的简单序列重复进行的遗传分析确定,HpmsE031标记与CM334和Chilsungcho变种杂交的F群体的653个个体中的Ptl1紧密相连。使用HpmsE031 SSR标记作为探针筛选了覆盖基因组12c的来自CM334的细菌人工染色体(BAC)文库,并鉴定了三个BAC克隆。 Ptl1区被一个80 kb BAC克隆TT1B7覆盖。荧光原位杂交(FISH)证实了TT1B7位于辣椒10号染色体。从TT1B7 BAC序列成功开发了一个共显性标记Tco和一个显性标记Tsca。 Tco从Ptl1向上映射0.33 cM,Tsca从Ptl1向下映射0.75 cM。 BAC序列的分析预测存在14个开放阅读框,包括60S核糖体蛋白L21样蛋白(Solanum demissum),蛋白激酶2(Nicotiana tabacum),假定蛋白和未命名的蛋白产物。这些结果不仅为辣椒中Ptl1的基于图的克隆提供有用的信息,而且为分析用Ptl1着墨的R基因簇提供了起点。

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