Instituto Valenciano de Investigaciones Agrarias (IVIA), Apartado Oficial, Moncada, Valencia, Spain.
Mol Plant Pathol. 2011 Aug;12(6):535-47. doi: 10.1111/j.1364-3703.2010.00691.x. Epub 2011 Jan 5.
Sharka disease, caused by the Plum pox virus (PPV), is one of the main limiting factors for stone fruit crops worldwide. Only a few resistance sources have been found in apricot (Prunus armeniaca L.), and most studies have located a major PPV resistance locus (PPVres) on linkage group 1 (LG1). However, the mapping accuracy was not sufficiently reliable and PPVres was predicted within a low confidence interval. In this study, we have constructed two high-density simple sequence repeat (SSR) improved maps with 0.70 and 0.68 markers/cm, corresponding to LG1 of 'Lito' and 'Goldrich' PPV-resistant cultivars, respectively. Using these maps, and excluding genotype-phenotype incongruent individuals, a new binary trait locus (BTL) analysis for PPV resistance was performed, narrowing down the PPVres support intervals to 7.3 and 5.9 cm in 'Lito' and 'Goldrich', respectively. Subsequently, 71 overlapping oligonucleotides (overgo) probes were hybridized against an apricot bacterial artificial chromosome (BAC) library, identifying 870 single BACs from which 340 were anchored onto a map region of approximately 30-40 cm encompassing PPVres. Partial BAC contigs assigned to the two allelic haplotypes (resistant/susceptible) of the PPVres locus were built by high-information content fingerprinting (HICF). In addition, a total of 300 BAC-derived sequences were obtained, and 257 showed significant homology with the peach genome scaffold_1 corresponding to LG1. According to the peach syntenic genome sequence, PPVres was predicted within a region of 2.16 Mb in which a few candidate resistance genes were identified.
李痘病由李痘病毒(PPV)引起,是全球核果作物的主要限制因素之一。在甜樱桃中仅发现少数几个抗性资源,大多数研究将一个主要的 PPV 抗性基因座(PPVres)定位在 1 号连锁群(LG1)上。然而,图谱的准确性不够可靠,PPVres 被预测在一个置信区间较低的区域内。本研究构建了两个高密度简单重复序列(SSR)图谱,分别对应于‘Lito’和‘Goldrich’两个抗 PPV 品种的 LG1,图谱标记密度为 0.70 和 0.68 个/cm。利用这两个图谱,排除基因型-表型不一致的个体,对 PPV 抗性进行了新的二项性状基因座(BTL)分析,将‘Lito’和‘Goldrich’的 PPVres 支持区间分别缩小到 7.3 和 5.9cm。随后,用 71 个重叠寡核苷酸(overgo)探针与甜樱桃细菌人工染色体(BAC)文库杂交,从约 30-40cm 的图谱区域中鉴定出 870 个单一 BAC,其中 340 个 BAC 被锚定到包含 PPVres 的区域。通过高信息量指纹图谱(HICF)构建了与 PPVres 基因座两个等位基因单体型(抗性/敏感)相对应的部分 BAC 连续图谱。此外,还获得了 300 个 BAC 衍生序列,其中 257 个序列与 LG1 对应的桃基因组支架_1 有显著同源性。根据桃的共线性基因组序列,预测 PPVres 位于 2.16Mb 的区域内,其中鉴定出几个候选抗性基因。