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基于紧密连锁的 DNA 微卫星和 RFLP 标记的大豆病毒抗性基因的分歧和等位基因关系。

Divergence and allelomorphic relationship of a soybean virus resistance gene based on tightly linked DNA microsatellite and RFLP markers.

机构信息

Department of Crop and Soil Environmental Sciences, Virginia Polytechnic Institute and State University Blacksburg, 24061, VA, USA.

出版信息

Theor Appl Genet. 1996 Jan;92(1):64-9. doi: 10.1007/BF00222952.

Abstract

The use of genetically diverse resistance sources is important in breeding for durable disease resistance. Detection and evaluation of resistance genes by conventional inheritance experiments, however, often require laborious screening and genetic testing. In the present study, a marker-assisted screening for resistance sources was initiated in soybean [Glycine max (L.) Merr] using one DNA microsatellite and two RFLP markers tightly linked to a soybean mosaic virus (SMV) resistance gene (Rsv1). The three marker loci were used to screen 67 diverse soybean cultivars, breeding lines, and plant introductions. Five variants were found at the microsatellite locus (HSP176L), and the two RFLP loci (pA186 and pK644a) near Rsv1 show a remarkably higher level of restriction polymorphism than Rsv1-independent RFLP loci. Several specific variants at the three marker loci were found to be correlated with virus resistance, among which HSP176L-2 can be detected by PCR, thus may be useful for germplasm screening. The grouping of the 67 accessions according to their multilocus marker variants agrees with the available pedigree information. When all, or most, of the cultivars within a given group with the same Rsv1-linked marker variant are resistant, their SMV resistance is most likely conferred by Rsv1. These putatively Rsv1-carrying groups contain a total of 38 SMV-resistant lines including six differential cultivars that are known to carry Rsv1. The remaining seven resistant accessions (Columbia, Holladay, Peking, Virginia, FFR-471, PI 507403, and PI 556949) do not carry resistance marker variants, and at least some of them could be sources of resistance genes independent of Rsv1.

摘要

利用遗传多样性的抗性资源在培育持久抗病性方面非常重要。然而,通过传统的遗传实验来检测和评估抗性基因通常需要费力的筛选和遗传测试。在本研究中,利用一个 DNA 微卫星和两个紧密连锁到大豆花叶病毒(SMV)抗性基因(Rsv1)的 RFLP 标记,对大豆[Glycine max(L.)Merr]中的抗性资源进行了标记辅助筛选。这三个标记位点用于筛选 67 个不同的大豆品种、品系和引种。在微卫星位点(HSP176L)发现了 5 个变体,而靠近 Rsv1 的两个 RFLP 位点(pA186 和 pK644a)显示出比 Rsv1 独立的 RFLP 位点更高的限制多态性水平。在三个标记位点发现了几个与病毒抗性相关的特定变体,其中 HSP176L-2 可以通过 PCR 检测,因此可能对种质筛选有用。根据其多基因座标记变体对 67 个品系进行分组与可用的系谱信息一致。当给定组内的所有或大多数品种都具有相同的与 Rsv1 连锁的标记变体且具有抗性时,它们的 SMV 抗性很可能由 Rsv1 赋予。这些假定携带 Rsv1 的群体共包含 38 个抗 SMV 品系,其中包括六个已知携带 Rsv1 的差异品种。其余 7 个抗性品系(哥伦比亚、霍拉代、北京、弗吉尼亚、FFR-471、PI 507403 和 PI 556949)不携带抗性标记变体,其中至少一些可能是独立于 Rsv1 的抗性基因的来源。

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