Guedira Mohammed, Xiong Mai, Hao Yuan Feng, Johnson Jerry, Harrison Steve, Marshall David, Brown-Guedira Gina
Department of Crop Science, North Carolina State University, Raleigh, North Carolina, 27695, United States of America.
Department of Crop and Soil Sciences, University of Georgia, Griffin, Georgia, 30223, United States of America.
PLoS One. 2016 May 10;11(5):e0154242. doi: 10.1371/journal.pone.0154242. eCollection 2016.
In wheat (Triticum aestivum L.), time from planting to spike emergence is influenced by genes controlling vernalization requirement and photoperiod response. Characterizing the available genetic diversity of known and novel alleles of VERNALIZATION1 (VRN1) and PHOTOPERIOD1 (PPD1) in winter wheat can inform approaches for breeding climate resilient cultivars. This study identified QTL for heading date (HD) associated with multiple VRN1 and PPD1 loci in a population developed from a cross between two early flowering winter wheat cultivars. When the population was grown in the greenhouse after partial vernalization treatment, major heading date QTLs co-located with the VRN-A1 and VRN-B1 loci. Copy number variation at the VRN-A1 locus influenced HD such that RIL having three copies required longer cold exposure to transition to flowering than RIL having two VRN-A1 copies. Sequencing vrn-B1 winter alleles of the parents revealed multiple polymorphisms in the first intron that were the basis of mapping a major HD QTL coinciding with VRN-B1. A 36 bp deletion in the first intron of VRN-B1 was associated with earlier HD after partial vernalization in lines having either two or three haploid copies of VRN-A1. The VRN1 loci interacted significantly and influenced time to heading in field experiments in Louisiana, Georgia and North Carolina. The PPD1 loci were significant determinants of heading date in the fully vernalized treatment in the greenhouse and in all field environments. Heading date QTL were associated with alleles having large deletions in the upstream regions of PPD-A1 and PPD-D1 and with copy number variants at the PPD-B1 locus. The PPD-D1 locus was determined to have the largest genetic effect, followed by PPD-A1 and PPD-B1. Our results demonstrate that VRN1 and PPD1 alleles of varying strength allow fine tuning of flowering time in diverse winter wheat growing environments.
在小麦(普通小麦)中,从播种到抽穗的时间受控制春化需求和光周期反应的基因影响。表征冬小麦中已知和新的春化基因1(VRN1)和光周期基因1(PPD1)等位基因的可用遗传多样性,可为培育适应气候变化的品种提供方法参考。本研究在两个早花冬小麦品种杂交产生的群体中,鉴定了与多个VRN1和PPD1位点相关的抽穗期(HD)QTL。当该群体在部分春化处理后在温室中种植时,主要抽穗期QTL与VRN - A1和VRN - B1位点共定位。VRN - A1位点的拷贝数变异影响抽穗期,使得具有三个拷贝的重组自交系(RIL)比具有两个VRN - A1拷贝的RIL需要更长的冷暴露时间才能过渡到开花。对亲本的vrn - B1冬性等位基因进行测序,发现在第一个内含子中有多个多态性,这是定位与VRN - B1重合的主要HD QTL的基础。VRN - B1第一个内含子中的36 bp缺失与具有两个或三个VRN - A1单倍体拷贝的品系在部分春化后较早的抽穗期相关。VRN1位点在路易斯安那州、佐治亚州和北卡罗来纳州的田间试验中相互作用显著,并影响抽穗时间。PPD1位点是温室中完全春化处理以及所有田间环境中抽穗期的重要决定因素。抽穗期QTL与PPD - A1和PPD - D1上游区域有大缺失的等位基因以及PPD - B1位点的拷贝数变异相关。确定PPD - D1位点具有最大的遗传效应,其次是PPD - A1和PPD - B1。我们的结果表明,不同强度的VRN1和PPD1等位基因可在不同的冬小麦生长环境中对开花时间进行微调。