Área de Genómica y Biotecnología, IFAPA-Centro Alameda del Obispo, Apdo 3092, E-14080, Córdoba, Spain.
BMC Plant Biol. 2021 Nov 22;21(1):551. doi: 10.1186/s12870-021-03335-5.
Ascochyta blight caused by Ascochyta fabae Speg. and broomrape (Orobanche crenata) are among the economically most significant pathogens of faba bean. Several QTLs conferring resistance against the two pathogens have been identified and validated in different genetic backgrounds. The aim of this study was to saturate the most stable QTLs for ascochyta and broomrape resistance in two Recombinant Inbred Line (RIL) populations, 29H x Vf136 and Vf6 x Vf136, to identify candidate genes conferring resistance against these two pathogens.
We exploited the synteny between faba bean and the model species Medicago truncatula by selecting a set of 219 genes encoding putative WRKY transcription factors and defense related proteins falling within the target QTL intervals, for genotyping and marker saturation in the two RIL populations. Seventy and 50 of the candidate genes could be mapped in 29H x Vf136 and Vf6 x Vf136, respectively. Besides the strong reduction of the QTL intervals, the mapping process allowed replacing previous dominant and pedigree-specific RAPD flanking markers with robust and transferrable SNP markers, revealing promising candidates for resistance against the two pathogens.
Although further efforts in association mapping and expression studies will be required to corroborate the candidate genes for resistance, the fine-mapping approach proposed here increases the genetic resolution of relevant QTL regions and paves the way for an efficient deployment of useful alleles for faba bean ascochyta and broomrape resistance through marker-assisted breeding.
由豌豆壳球腔菌(Ascochyta fabae Speg.)和列当(Orobanche crenata)引起的褐斑病和列当属寄生植物是最具经济重要性的蚕豆病原菌之一。已经在不同的遗传背景下鉴定和验证了几个对这两种病原体具有抗性的 QTL。本研究的目的是饱和在两个重组自交系(RIL)群体 29H x Vf136 和 Vf6 x Vf136 中最稳定的抗褐斑病和列当属的 QTL,以鉴定对这两种病原体具有抗性的候选基因。
我们通过选择一组 219 个编码假定 WRKY 转录因子和防御相关蛋白的基因,利用蚕豆与模式物种蒺藜苜蓿之间的同线性,将其落入目标 QTL 区间内,用于在两个 RIL 群体中进行基因分型和标记饱和。在 29H x Vf136 和 Vf6 x Vf136 中,分别有 70 和 50 个候选基因可以被映射。除了 QTL 区间的强烈缩小外,映射过程还允许用稳健且可转移的 SNP 标记替代先前的显性和系谱特异性 RAPD 侧翼标记,为两种病原体的抗性揭示了有希望的候选基因。
尽管需要进一步进行关联作图和表达研究来验证抗性候选基因,但这里提出的精细映射方法增加了相关 QTL 区域的遗传分辨率,并为通过标记辅助选择有效地部署有用的蚕豆抗褐斑病和列当属的等位基因铺平了道路。