Segovia-Lerma A, Cantrell R G, Conway J M, Ray I M
Facultad de Ciencias Agrícolas y Forestales, Universidad Autónoma de Chihuahua, Km. 2 1/2 Carretera Delicias-Rosales, Ciudad Delicias, Chihuahua, C.P. 33000, México.
Genome. 2003 Feb;46(1):51-8. doi: 10.1139/g02-100.
Improving commercial utilization of perennial Medicago collections requires developing approaches that can rapidly and accurately characterize genetic diversity among large numbers of populations. This study evaluated the potential of using amplified fragment length polymorphism (AFLP) DNA markers, in combination with DNA bulking over multiple genotypes, as a strategy for high-throughput characterization of genetic distances (D) among alfalfa (Medicago sativa L.) accessions. Bulked DNA templates from 30 genotypes within each of nine well-recognized germplasms (African, Chilean, Flemish, Indian, Ladak, Medicago sativa subsp. falcata, Medicago sativa subsp. varia, Peruvian, and Turkistan) were evaluated using 34 primer combinations. A total of 3754 fragments were identified, of which 1541 were polymorphic. The number of polymorphic fragments detected per primer combination ranged from 20 to 85. Pairwise D estimates among the nine germplasms ranged from 0.52 to 1.46 with M. sativa subsp. falcata being the most genetically dissimilar. Unweighted pair-group method arithmetic average (UPGMA) analysis of the marker data produced two main clusters, (i) M. sativa subsp. sativa and M. sativa subsp. varia, and (ii) M. sativa subsp. falcata. Cluster-analysis results and D estimates among the Chilean, Peruvian, Flemish, and M. sativa subsp. varia germplasms supported the hypothesis that Peruvian was more similar to original Spanish introductions into Central and South America than Chilean. Hierarchical arrangement of the nine germplasms was supported by their respective geographic, subspecific, and intersubspecific hybrid origins. Subsets of as few as seven highly informative primer pairs were identified that produced comparable D estimates and similar heirarchical arrangements compared with the complete dataset. The results indicate that use of primer-pair subsets for AFLP analysis of bulk DNA templates could serve as a high-throughput system for accurately characterizing genetic diversity among large numbers of alfalfa populations.
提高多年生苜蓿种质资源的商业利用率需要开发能够快速、准确地表征大量群体间遗传多样性的方法。本研究评估了使用扩增片段长度多态性(AFLP)DNA标记,并结合多个基因型的DNA混合池,作为高通量表征苜蓿(Medicago sativa L.)种质间遗传距离(D)的一种策略。使用34对引物组合对9个公认种质(非洲、智利、佛兰德、印度、拉达克、紫花苜蓿亚种黄花苜蓿、紫花苜蓿亚种杂花苜蓿、秘鲁和突厥斯坦)中每个种质的30个基因型的混合DNA模板进行了评估。共鉴定出3754个片段,其中1541个为多态性片段。每个引物组合检测到的多态性片段数量在20至85个之间。9个种质间的成对D估计值在0.52至1.46之间,其中黄花苜蓿亚种的遗传差异最大。对标记数据进行非加权组平均法(UPGMA)分析产生了两个主要聚类,(i)紫花苜蓿亚种紫花苜蓿和紫花苜蓿亚种杂花苜蓿,以及(ii)黄花苜蓿亚种。智利、秘鲁、佛兰德和紫花苜蓿亚种杂花苜蓿种质间的聚类分析结果和D估计值支持了这样的假设,即秘鲁种质比智利种质更类似于最初引入中美洲和南美洲的西班牙种质。9个种质的层次排列得到了它们各自地理、亚种和种间杂交起源的支持。鉴定出了少至7对高度信息丰富的引物对组成的子集,与完整数据集相比,它们产生了可比的D估计值和相似的层次排列。结果表明, 使用引物对子集对混合DNA模板进行AFLP分析可作为一种高通量系统,用于准确表征大量苜蓿群体间的遗传多样性。