ENEA, Casaccia Research Centre, Via Anguillarese 301, 00123, Rome, Italy.
SCUOLA SUPERIORE SANT'ANNA, Piazza Martiri della Libertà 33, 56127, Pisa, Italy.
Planta. 2018 Feb;247(2):459-469. doi: 10.1007/s00425-017-2799-0. Epub 2017 Oct 26.
A and B genome copies of DRF1 gene in durum wheat were isolated and sequenced using gene variability. B genome specific polymorphism resulted, in a RIL population, in relationship with grain yield mainly in drought condition. Drought tolerance is one of the main components of yield potential and stability, and its improvement is a major challenge to breeders. Transcription factors are considered among the best candidate genes for developing functional markers, since they are components of the signal transduction pathways that coordinate the expression of several downstream genes. Polymorphisms of the Triticum durum dehydration responsive factor 1 (TdDRF1) gene that belongs to DREB2 transcription factor family were identified and specifically assigned to the A or B genome. A panel of primers was derived to selectively isolate the corresponding gene copies. These molecular information were also used to develop a new molecular marker: an allele-specific PCR assay discriminating two genotypes (Mohawk and Cocorit) was developed and used for screening a durum wheat recombinant inbred line population (RIL-pop) derived from the above genotypes. Phenotypic data from the RIL-pop grown during two seasons, under different environmental conditions, adopting an α-lattice design with two repetitions, were collected, analyzed and correlated with molecular data from the PCR assay. A significant association between a specific polymorphism in the B genome copy of the TdDRF1 gene and the grain yield in drought conditions were observed.
使用基因变异,分离并测序了硬粒小麦中 DRF1 基因的 A 和 B 基因组拷贝。在 RIL 群体中,B 基因组特异性多态性与主要在干旱条件下的粒产量有关。耐旱性是产量潜力和稳定性的主要组成部分之一,其改良是培育者面临的主要挑战。转录因子被认为是开发功能标记的最佳候选基因之一,因为它们是协调几个下游基因表达的信号转导途径的组成部分。鉴定了属于 DREB2 转录因子家族的硬粒小麦脱水响应因子 1 (TdDRF1) 基因的多态性,并将其特异性分配到 A 或 B 基因组。设计了一组引物来选择性地分离相应的基因拷贝。这些分子信息还用于开发一种新的分子标记:开发了一种等位基因特异性 PCR 分析,可区分两种基因型(Mohawk 和 Cocorit),并用于筛选来自上述基因型的硬粒小麦重组自交系群体(RIL-pop)。在两个季节、不同环境条件下采用α-格子设计进行两次重复的 RIL-pop 的表型数据进行了收集、分析,并与 PCR 分析的分子数据进行了相关性分析。在 B 基因组拷贝的 TdDRF1 基因的特定多态性与干旱条件下的粒产量之间观察到显著关联。