Triticeae Research Institute, Sichuan Agricultural University, Wenjiang, Chengdu, Sichuan, 611130, PR China.
BMC Genet. 2012 Aug 13;13:69. doi: 10.1186/1471-2156-13-69.
A synthetic doubled-haploid hexaploid wheat population, SynDH1, derived from the spontaneous chromosome doubling of triploid F1 hybrid plants obtained from the cross of hybrids Triticum turgidum ssp. durum line Langdon (LDN) and ssp. turgidum line AS313, with Aegilops tauschii ssp. tauschii accession AS60, was previously constructed. SynDH1 is a tetraploidization-hexaploid doubled haploid (DH) population because it contains recombinant A and B chromosomes from two different T. turgidum genotypes, while all the D chromosomes from Ae. tauschii are homogenous across the whole population. This paper reports the construction of a genetic map using this population.
Of the 606 markers used to assemble the genetic map, 588 (97%) were assigned to linkage groups. These included 513 Diversity Arrays Technology (DArT) markers, 72 simple sequence repeat (SSR), one insertion site-based polymorphism (ISBP), and two high-molecular-weight glutenin subunit (HMW-GS) markers. These markers were assigned to the 14 chromosomes, covering 2048.79 cM, with a mean distance of 3.48 cM between adjacent markers. This map showed good coverage of the A and B genome chromosomes, apart from 3A, 5A, 6A, and 4B. Compared with previously reported maps, most shared markers showed highly consistent orders. This map was successfully used to identify five quantitative trait loci (QTL), including two for spikelet number on chromosomes 7A and 5B, two for spike length on 7A and 3B, and one for 1000-grain weight on 4B. However, differences in crossability QTL between the two T. turgidum parents may explain the segregation distortion regions on chromosomes 1A, 3B, and 6B.
A genetic map of T. turgidum including 588 markers was constructed using a synthetic doubled haploid (SynDH) hexaploid wheat population. Five QTLs for three agronomic traits were identified from this population. However, more markers are needed to increase the density and resolution of this map in the future study.
从自发染色体加倍的三倍体 F1 杂种植物中衍生出的合成双单倍体六倍体小麦群体 SynDH1,这些杂种植物是由硬粒小麦品种 Langdon(LDN)和普通小麦品种 AS313 的杂交种与节节麦 Ae. tauschii ssp. tauschii 品系 AS60 杂交获得的。SynDH1 是一个四倍体化六倍体双单倍体(DH)群体,因为它包含来自两个不同硬粒小麦基因型的 A 和 B 染色体的重组,而 Ae. tauschii 的所有 D 染色体在整个群体中都是同质的。本文报道了使用该群体构建遗传图谱的情况。
用于组装遗传图谱的 606 个标记中,有 588 个(97%)被分配到连锁群中。这些标记包括 513 个多样性阵列技术(DArT)标记、72 个简单序列重复(SSR)标记、1 个插入位点多态性(ISBP)标记和 2 个高分子量谷蛋白亚基(HMW-GS)标记。这些标记被分配到 14 条染色体上,覆盖了 2048.79cM,相邻标记之间的平均距离为 3.48cM。除了 3A、5A、6A 和 4B 之外,该图谱很好地覆盖了 A 和 B 基因组染色体。与以前报道的图谱相比,大多数共享标记显示出高度一致的顺序。该图谱成功地用于鉴定五个数量性状位点(QTL),包括位于 7A 和 5B 染色体上的 5 个小穗数 QTL、位于 7A 和 3B 染色体上的 2 个穗长 QTL,以及位于 4B 染色体上的 1 个千粒重 QTL。然而,两个硬粒小麦亲本之间的可交配性 QTL 的差异可能解释了 1A、3B 和 6B 染色体上的分离扭曲区域。
利用合成双单倍体(SynDH)六倍体小麦群体构建了硬粒小麦的遗传图谱,图谱包含 588 个标记。从该群体中鉴定出 5 个与 3 个农艺性状相关的 QTL。然而,未来的研究需要更多的标记来增加图谱的密度和分辨率。