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主茎的茸毛密度与辣椒(Capsicum annuum L.)对 PepMoV 的抗性密切相关。

Trichome density of main stem is tightly linked to PepMoV resistance in chili pepper (Capsicum annuum L.).

机构信息

Department of Plant Sciences and Plant Genomics and Breeding Institute, Seoul National University, Seoul, Korea.

出版信息

Theor Appl Genet. 2011 Apr;122(6):1051-8. doi: 10.1007/s00122-010-1510-7. Epub 2010 Dec 24.

DOI:10.1007/s00122-010-1510-7
PMID:21184049
Abstract

A relationship between pepper trichome and pepper mottle virus (PepMoV) resistance was examined. In an intraspecific F(2) mapping population from the cross between Capsicum annuum CM334 (trichome-bearing and PepMoV resistant) and Chilsungcho (glabrous and PepMoV susceptible), major QTLs for both traits were identified by composite interval mapping in linkage group (LG) 24 corresponding a telomere region on pepper chromosome 10. Ptel1 of putative trichome enhancing locus was a common major QTL for trichome density on the main stem and calyx. Ptel1 apart from HpmsE031 at a 1.03 cM interval was specifically associated to the trichome density on the main stem, whereas Ptel2 near m104 marker on LG2 was specific for the calyx trichome. Epistatic analysis indicated that Ptel1 engaged in controlling the trichome density by mutual interactions with the organ-specific QTLs. For PepMoV resistance, two QTLs (Pep1 and Pep2) were identified on the LG 24. Pep1 was located with Ptel1 in the R-gene cluster (RGC) for potyvirus resistance including Pvr4 with broad spectrum resistance to potyviruses. Pep1 flanking TG420 marker seemed to be the major factors determining correlation with PepMoV resistance. These results indicate that the level of trichome density on pepper main stem can be used as a morphological marker for Pvr4 in pepper breeding.

摘要

研究了辣椒刺毛和辣椒斑驳病毒(PepMoV)抗性之间的关系。在辣椒品种 CM334(有刺毛和 PepMoV 抗性)和 Chilsungcho(无刺毛和 PepMoV 敏感)杂交的种内 F2 作图群体中,通过复合区间作图法在对应于辣椒第 10 号染色体端粒区域的第 24 条连锁群(LG)上鉴定出了这两个性状的主要 QTL。假定的刺毛增强基因座 Ptel1 是主茎和花萼刺毛密度的主要 QTL。Ptel1 除了在 1.03cM 间隔处的 HpmsE031 外,还与主茎刺毛密度特异性相关,而位于 LG2 上的 m104 标记附近的 Ptel2 则与花萼刺毛特异性相关。上位性分析表明,Ptel1 通过与器官特异性 QTL 的相互作用来控制刺毛密度。对于 PepMoV 抗性,在第 24 条 LG 上鉴定出了两个 QTL(Pep1 和 Pep2)。Pep1 位于包括对多种病毒具有广谱抗性的 Pvr4 在内的 R 基因簇(RGC)中与 Ptel1 相邻。与 PepMoV 抗性相关的主要因素似乎是位于 Pep1 侧翼 TG420 标记附近的区域。这些结果表明,辣椒主茎上刺毛密度的水平可以作为辣椒育种中 Pvr4 的形态标记。

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