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首页> 外文期刊>Genome Biology >Transcriptomic analysis of wheat near-isogenic lines identifies PM19-A1 and A2 as candidates for a major dormancy QTL
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Transcriptomic analysis of wheat near-isogenic lines identifies PM19-A1 and A2 as candidates for a major dormancy QTL

机译:小麦近等基因系的转录组学分析确定PM19-A1和A2是主要休眠QTL的候选基因

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Background: Next-generation sequencing technologies provide new opportunities to identify the genetic components responsible for trait variation. However, in species with large polyploid genomes, such as bread wheat, the ability to rapidly identify genes underlying quantitative trait loci (QTL) remains non-trivial. To overcome this, we introduce a novel pipeline that analyses, by RNA-sequencing, multiple near-isogenic lines segregating for a targeted QTL. Results: We use this approach to characterize a major and widely utilized seed dormancy QTL located on chromosome 4AL. It exploits the power and mapping resolution afforded by large multi-parent mapping populations, whilst reducing complexity by using multi-allelic contrasts at the targeted QTL region. Our approach identifies two adjacent candidate genes within the QTL region belonging to the ABA-induced Wheat Plasma Membrane 19 family. One of them, PM19-A1, is highly expressed during grain maturation in dormant genotypes. The second, PM19-A2, shows changes in sequence causing several amino acid alterations between dormant and non-dormant genotypes. We confirm that PM19 genes are positive regulators of seed dormancy. Conclusions: The efficient identification of these strong candidates demonstrates the utility of our transcriptomic pipeline for rapid QTL to gene mapping. By using this approach we are able to provide a comprehensive genetic analysis of the major source of grain dormancy in wheat. Further analysis across a diverse panel of bread and durum wheats indicates that this important dormancy QTL predates hexaploid wheat. The use of these genes by wheat breeders could assist in the elimination of pre-harvest sprouting in wheat.
机译:背景:下一代测序技术为鉴定导致性状变异的遗传成分提供了新的机会。但是,在具有大量多倍体基因组的物种(例如面包小麦)中,快速识别定量性状基因位点(QTL)基础基因的能力仍然很重要。为了克服这个问题,我们引入了一种新颖的流水线,该流水线通过RNA测序分析了多个针对目标QTL的近等基因系。结果:我们使用这种方法来表征位于4AL染色体上的主要且广泛使用的种子休眠QTL。它利用了大型多亲本制图群体提供的功能和制图分辨率,同时通过在目标QTL区域使用多等位基因对比来降低复杂性。我们的方法在QTL区域内鉴定了两个相邻的候选基因,它们属于ABA诱导的小麦血浆膜19家族。其中之一,PM19-A1,在处于休眠基因型的谷物成熟过程中高度表达。第二个是PM19-A2,显示序列变化,导致休眠和非休眠基因型之间发生多个氨基酸改变。我们证实,PM19基因是种子休眠的正向调节剂。结论:对这些强候选人的有效鉴定证明了我们的转录组学管道可用于快速QTL基因定位。通过使用这种方法,我们能够对小麦休眠的主要来源进行全面的遗传分析。对面包和硬粒小麦的不同研究小组的进一步分析表明,这种重要的休眠QTL早于六倍体小麦。小麦育种者使用这些基因可以帮助消除小麦收获前的发芽。

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