Centro de Protección Vegetal y Biotecnología, Instituto Valenciano de Investigaciones Agrarias. Moncada, Valencia, Spain.
PLoS One. 2013 Oct 8;8(10):e76755. doi: 10.1371/journal.pone.0076755. eCollection 2013.
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 ACT-toxin. SSR and SNP markers were developed for efficient early marker-assisted selection of ABS resistant hybrids.
在多倍体物种中,表型性状的遗传分析和标记与性状的关联通常被认为是一个挑战。在本工作中,利用第二次分裂还原(SDR)产生的 2n 配子的特殊遗传结构,结合了不同的方法,以定位与三倍体柑橘后代中对褐点病(ABS)抗性相关的基因组区域。柑橘中的 ABS 是由真菌交链格孢Alternaria alternata 的桔生病原体引起的严重疾病。该病原体产生 ACT 毒素,在易感基因型上诱导果实和幼叶坏死斑、落叶和落果。对于旨在生产无核柑橘品种的三倍体育种计划来说,这是一个强烈关注的问题。基于二倍体群体研究提出的易感性单基因显性遗传,在三倍体后代中得到了证实。利用大量遗传图谱 SNP 标记进行的单体型分离分析与基因组扫描,以及利用 SSR 和 SNP 标记进行的半四分体分析的靶向遗传作图,允许在染色体 III 着丝粒附近定位到与 ABS 抗性相关的 3.3Mb 基因组区域。通过对该基因组区域的基因本体分析,鉴定出了一些抗性基因簇。其中一些基因是控制 ACT 毒素显性易感性的良好候选基因。开发了 SSR 和 SNP 标记,用于高效地早期进行 ABS 抗性杂种的标记辅助选择。