Zhang Yingjun, Xia Xianchun, He Zhonghu
Institute of Crop Science, National Wheat Improvement Center, Chinese Academy of Agricultural Sciences (CAAS), 12 Zhongguancun South Street, Beijing, 100081, China.
Institute of Cereal and Oil Crops, Hebei Academy of Agriculture and Forestry Sciences, 162 Hengshan Street, Shijiazhuang, 050035, China.
Theor Appl Genet. 2017 Jan;130(1):81-89. doi: 10.1007/s00122-016-2793-0. Epub 2016 Sep 20.
We cloned TaSdr - A1 gene, and developed a gene-specific marker for TaSdr - A1 . A QTL for germination index at the TaSdr - A1 locus was identified in the Yangxiaomai/Zhongyou 9507 RIL population. Pre-harvest sprouting (PHS) affects yield and end-use quality in bread wheat (Triticum aestivum L.). In the present study we found an association between the TaSdr-A1 gene and PHS tolerance in bread wheat. TaSdr-A1 on chromosome 2A was cloned using a homologous cloning approach. Sequence analysis of TaSdr-A1 revealed an SNP at position 643, with the G allele being present in genotypes with lower germination index (GI) values and A in those with higher GI. These alleles were designated as TaSdr-A1a and TaSdr-A1b, respectively. A cleaved amplified polymorphism sequence (CAPS) marker Sdr2A based on the SNP was developed, and linkage mapping and QTL analysis were conducted to confirm the association between TaSdr-A1 and seed dormancy. Sdr2A was located in a 2.9 cM interval between SSR markers Xgwm95 and Xgwm372. A QTL for GI at the TaSdr-A1 locus explained 6.6, 7.3, and 8.2 % of the phenotypic variances in a Yangxiaomai/Zhongyou 9507 RIL population grown at Beijing, Shijiazhuang, and the averaged data from the two environments, respectively. Two sets of Chinese wheat cultivars used for validating the TaSdr-A1 polymorphism and the corresponding gene-specific marker Sdr2A showed that TaSdr-A1 was significantly associated with GI. Among 29 accessions with TaSdr-A1a, 24 (82.8 %) were landraces, indicating the importance of Chinese wheat landraces as sources of PHS tolerance. This study identified a novel PHS resistance allele TaSdr-A1a mainly presented in Chinese landraces and it is likely to be the causal gene for QPhs.ccsu-2A.3, providing new information for an understanding of seed dormancy.
我们克隆了TaSdr - A1基因,并开发了一种针对TaSdr - A1的基因特异性标记。在小偃麦/中优9507重组自交系群体中,在TaSdr - A1位点鉴定到一个与发芽指数相关的数量性状位点(QTL)。收获前发芽(PHS)会影响面包小麦(普通小麦)的产量和最终使用品质。在本研究中,我们发现面包小麦中TaSdr - A1基因与PHS耐受性之间存在关联。利用同源克隆方法克隆了2A染色体上的TaSdr - A1。TaSdr - A1的序列分析显示在第643位存在一个单核苷酸多态性(SNP),发芽指数(GI)值较低的基因型中存在G等位基因,而GI值较高的基因型中存在A等位基因。这些等位基因分别被命名为TaSdr - A1a和TaSdr - A1b。基于该SNP开发了一种酶切扩增多态性序列(CAPS)标记Sdr2A,并进行连锁图谱构建和QTL分析以确认TaSdr - A1与种子休眠之间的关联。Sdr2A位于SSR标记Xgwm95和Xgwm372之间2.9厘摩的区间内。在分别于北京、石家庄种植的小偃麦/中优9507重组自交系群体以及这两个环境的平均数据中,TaSdr - A1位点的GI QTL分别解释了6.6%、7.3%和8.2%的表型变异。用于验证TaSdr - A1多态性及相应基因特异性标记Sdr2A的两组中国小麦品种表明,TaSdr - A1与GI显著相关。在29个具有TaSdr - A1a的材料中,有24个(82.8%)是地方品种,这表明中国小麦地方品种作为PHS耐受性来源的重要性。本研究鉴定出一个主要存在于中国地方品种中的新型PHS抗性等位基因TaSdr - A1a,它可能是QPhs.ccsu - 2A.3的因果基因,为理解种子休眠提供了新信息。