Cook David E, Bayless Adam M, Wang Kai, Guo Xiaoli, Song Qijian, Jiang Jiming, Bent Andrew F
Department of Plant Pathology (D.E.C., A.M.B., X.G., A.F.B.) and Department of Horticulture (K.W., J.J.), University of Wisconsin, Madison, Wisconsin 53706; andSoybean Genomics and Improvement Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, Maryland 20705 (Q.S.).
Department of Plant Pathology (D.E.C., A.M.B., X.G., A.F.B.) and Department of Horticulture (K.W., J.J.), University of Wisconsin, Madison, Wisconsin 53706; andSoybean Genomics and Improvement Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, Maryland 20705 (Q.S.)
Plant Physiol. 2014 Jun;165(2):630-647. doi: 10.1104/pp.114.235952. Epub 2014 Apr 14.
Copy number variation of kilobase-scale genomic DNA segments, beyond presence/absence polymorphisms, can be an important driver of adaptive traits. Resistance to Heterodera glycines (Rhg1) is a widely utilized quantitative trait locus that makes the strongest known contribution to resistance against soybean cyst nematode (SCN), Heterodera glycines, the most damaging pathogen of soybean (Glycine max). Rhg1 was recently discovered to be a complex locus at which resistance-conferring haplotypes carry up to 10 tandem repeat copies of a 31-kb DNA segment, and three disparate genes present on each repeat contribute to SCN resistance. Here, we use whole-genome sequencing, fiber-FISH (fluorescence in situ hybridization), and other methods to discover the genetic variation at Rhg1 across 41 diverse soybean accessions. Based on copy number variation, transcript abundance, nucleic acid polymorphisms, and differentially methylated DNA regions, we find that SCN resistance is associated with multicopy Rhg1 haplotypes that form two distinct groups. The tested high-copy-number Rhg1 accessions, including plant introduction (PI) 88788, contain a flexible number of copies (seven to 10) of the 31-kb Rhg1 repeat. The identified low-copy-number Rhg1 group, including PI 548402 (Peking) and PI 437654, contains three copies of the Rhg1 repeat and a newly identified allele of Glyma18g02590 (a predicted α-SNAP [α-soluble N-ethylmaleimide-sensitive factor attachment protein]). There is strong evidence for a shared origin of the two resistance-conferring multicopy Rhg1 groups and subsequent independent evolution. Differentially methylated DNA regions also were identified within Rhg1 that correlate with SCN resistance. These data provide insights into copy number variation of multigene segments, using as the example a disease resistance trait of high economic importance.
除了存在/缺失多态性之外,千碱基规模的基因组DNA片段的拷贝数变异可能是适应性性状的重要驱动因素。对大豆胞囊线虫(Heterodera glycines)的抗性(Rhg1)是一个广泛利用的数量性状位点,对抵抗大豆胞囊线虫(SCN,Heterodera glycines)——大豆(Glycine max)最具破坏性的病原体——贡献最大。最近发现Rhg1是一个复杂的位点,赋予抗性的单倍型在该位点携带多达10个31-kb DNA片段的串联重复拷贝,并且每个重复上存在的三个不同基因有助于对SCN的抗性。在这里,我们使用全基因组测序、纤维荧光原位杂交(fiber-FISH)和其他方法来发现41个不同大豆种质中Rhg1的遗传变异。基于拷贝数变异、转录本丰度、核酸多态性和差异甲基化DNA区域,我们发现对SCN的抗性与形成两个不同组的多拷贝Rhg1单倍型相关。测试的高拷贝数Rhg1种质,包括植物引种(PI)88788,含有31-kb Rhg1重复的可变拷贝数(7至10个)。鉴定出的低拷贝数Rhg1组,包括PI 548402(北京)和PI 437654,含有Rhg1重复的三个拷贝以及一个新鉴定的Glyma18g02590等位基因(一种预测的α-SNAP [α-可溶性N-乙基马来酰亚胺敏感因子附着蛋白])。有强有力的证据表明两个赋予抗性的多拷贝Rhg1组有共同的起源以及随后的独立进化。在Rhg1内还鉴定出与SCN抗性相关的差异甲基化DNA区域。这些数据以一种具有高度经济重要性的抗病性状为例,为多基因片段的拷贝数变异提供了见解。