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Genetically based location from triploid populations and gene ontology of a 3.3-Mb genome region linked to alternaria brown spot resistance in citrus reveal clusters of resistance genes

机译:来自三倍体种群的遗传定位以及与柑橘中黑斑病褐斑病抗性有关的3.3 Mb基因组区域的基因本体揭示了抗性基因簇

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摘要

Genetic analysis of phenotypical traits and marker-trait association in polyploid species is generally considered as a challenge. In the present work, different approaches were combined taking advantage of the particular genetic structures of 2n gametes resulting from second division restitution (SDR) to map a genome region linked to Alternaria brown spot (ABS) resistance in triploid citrus progeny. ABS in citrus is a serious disease caused by the tangerine pathotype of the fungus Alternaria alternata. This pathogen produces ACT-toxin, which induces necrotic lesions on fruit and young leaves, defoliation and fruit drop in susceptible genotypes. It is a strong concern for triploid breeding programs aiming to produce seedless mandarin cultivars. The monolocus dominant inheritance of susceptibility, proposed on the basis of diploid population studies, was corroborated in triploid progeny. Bulk segregant analysis coupled with genome scan using a large set of genetically mapped SNP markers and targeted genetic mapping by half tetrad analysis, using SSR and SNP markers, allowed locating a 3.3 Mb genomic region linked to ABS resistance near the centromere of chromosome III. Clusters of resistance genes were identified by gene ontology analysis of this genomic region. Some of these genes are good candidates to control the dominant susceptibility to the ACTtoxin. SSR and SNP markers were developed for efficient early marker-assisted selection of ABS resistant hybrids. (Résumé d'auteur)
机译:多倍体物种的表型性状和标记-性状关联的遗传分析通常被认为是一项挑战。在目前的工作中,利用第二分裂恢复(SDR)产生的2n配子的特殊遗传结构,结合了不同的方法,以绘制与三倍体柑橘后代中链格孢褐斑病(ABS)抗性相关的基因组区域。柑橘中的ABS是一种严重的疾病,它是由真菌Alternaria alternata的橘子病型引起的。这种病原体产生ACT毒素,从而诱发易感基因型的果实和幼叶坏死性病变,脱叶和果实掉落。对于旨在生产无核普通话品种的三倍体育种计划,这是一个非常关注的问题。在二倍体种群研究的基础上提出的易感性的单基因显性遗传在三倍体后代中得到了证实。大量隔离分析与基因组扫描结合使用大量的基因定位的SNP标记,并通过半四分体分析(使用SSR和SNP标记,通过半四分位分析进行靶向的基因定位),可以在3.3号染色体的着丝粒附近定位与ABS抗性相关的3.3 Mb基因组区域。通过对该基因组区域的基因本体分析来鉴定抗性基因的簇。这些基因中的某些是控制ACTtoxin显性易感性的良好候选者。开发了SSR和SNP标记,可进行有效的早期标记辅助选择ABS抗性杂种。 (Résuméd'auteur)

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