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Bin mapping of tomato diversity array (DArT) markers to genomic regions of Solanum lycopersicum x Solanum pennellii introgression lines

机译:番茄多样性阵列(DarT)标记与番茄solanum pennellii基因渗入系基因组区域的Bin作图

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摘要

Marker-trait association studies in tomato haveprogressed rapidly due to the availability of several populationsdeveloped between wild species and domesticatedtomato. However, in the absence of whole genomesequences for each wild species, molecular marker methodsfor whole genome comparisons and Wne mapping arerequired. We describe the development and validation of adiversity arrays technology (DArT) platform for tomatousing an introgression line (IL) population consisting ofwild Solanum pennellii introgressed into Solanum lycopersicum(cv. M82). A tomato diversity array consisting of6,912 clones from domesticated tomato and twelve wildtomato/Solanaceous species was constructed. We successfullybin-mapped 990 polymorphic DArT markers togetherwith 108 RFLP markers across the IL population, increasingthe number of markers available for each S. pennelliiintrogression by tenfold on average. A subset of DArTmarkers from ILs previously associated with increased levelsof lycopene and carotene were sequenced, and 44%matched protein coding genes. The bin-map position andorder of sequenced DArT markers correlated well withtheir physical position on scaVolds of the draft tomatogenome sequence (SL2.40). The utility of sequenced DArTmarkers was illustrated by converting several markers inboth the S. pennellii and S. lycopersicum phases to cleavedampliWed polymorphic sequence (CAPS) markers. Genotypescores from the CAPS markers conWrmed the genotypescores from the DArT hybridizations used to constructthe bin map. The tomato diversity array provides additional“sequence-characterized” markers for Wne mapping ofQTLs in S. pennellii ILs and wild tomato species.
机译:番茄的标记性状关联研究由于在野生物种和家养番茄之间发育的几个种群的可用性而迅速发展。然而,在没有每种野生物种的全基因组序列的情况下,需要用于全基因组比较和Wne作图的分子标记方法。我们描述了番茄的多样性阵列技术(DArT)平台的开发和验证,该平台使用了由渗入番茄茄(C82.M82)的野生茄(Solanum pennellii)组成的渗入系(IL)种群。构建了番茄多样性阵列,该阵列由来自驯化番茄的6,912个克隆和十二个野生番茄/茄科物种组成。我们成功地在整个IL人群中将990个多态性DArT标记与108个RFLP标记一起进行了映射,使每个S. pennellii基因渗入可用的标记数平均增加了十倍。对先前与番茄红素和胡萝卜素水平升高相关的ILs的DArTmarker子集进行了测序,并匹配了44%的蛋白质编码基因。序列DArT标记的bin图位置和顺序与其在番茄基因组草图序列(SL2.40)的scaVolds上的物理位置密切相关。通过将Pennellii和S.lycopersicum相中的几个标记转换为裂解的多态序列(CAPS)标记,说明了测序DArTmarker的用途。来自CAPS标记的基因型分数证实了来自用于构建bin图的DArT杂交的基因型分数。番茄多样性阵列提供了额外的“序列特征化”标记,用于对半边链球菌IL和野生番茄物种中的QTL进行Wne定位。

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