Maughan P J, Saghi Maroof M A, Buss G R
Department of Crop and Soil Environmental Sciences, Virginia Polytechnic Institute and State University, Blacksburg 24061, USA.
Genome. 1995 Aug;38(4):715-23. doi: 10.1139/g95-090.
The objectives of this study were to (i) assess the extent of genetic variation in soybean microsatellites (simple sequence repeats or SSRs), (ii) assay for amplified sequence length polymorphisms (ASLPs), and (iii) evaluate the usefulness of SSRs and ASLPs as genetic markers. Five microsatellites detected a total of 79 variants (alleles) in a sample of 94 accessions of wild (Glycine soja) and cultivated soybean (G. max). F2 segregation analysis of four of the five microsatellites identified these variants (alleles) with four loci located in independent linkage groups. The number of alleles per microsatellite locus ranged from 5 to 21; to our knowledge these are the largest numbers of alleles for single Mendelian loci reported in soybean. Allelic diversity for the SSR loci was greater in wild than in cultivated soybean. Overall, 43 more SSR alleles were detected in wild than in cultivated soybean. These results indicate that SSRs are the marker of choice, especially for species with low levels of variation as detected by other types of markers. Two alleles were detected at each of the three ASLP loci examined. A total of six ASLP alleles were observed in cultivated soybean and five were observed in wild soybean; all alleles detected in wild soybean were present in cultivated soybean. Allelic diversity values for the ASLP loci were near previous estimates for restriction fragment length polymorphisms and therefore ASLPs may be useful as genetic markers in site-directed mapping.
(i)评估大豆微卫星(简单序列重复或SSRs)的遗传变异程度;(ii)检测扩增序列长度多态性(ASLPs);(iii)评估SSR和ASLP作为遗传标记的实用性。五个微卫星在94份野生大豆(野生大豆)和栽培大豆(大豆)样本中共检测到79个变异(等位基因)。对五个微卫星中的四个进行F2分离分析,确定这些变异(等位基因)位于四个独立连锁群中的四个位点。每个微卫星位点的等位基因数量从5到21不等;据我们所知,这些是大豆中报道的单个孟德尔位点的最大等位基因数量。野生大豆中SSR位点的等位基因多样性高于栽培大豆。总体而言,野生大豆中检测到的SSR等位基因比栽培大豆多43个。这些结果表明,SSR是首选标记,特别是对于其他类型标记检测到变异水平较低的物种。在所检测的三个ASLP位点中,每个位点都检测到两个等位基因。在栽培大豆中总共观察到六个ASLP等位基因,在野生大豆中观察到五个;在野生大豆中检测到的所有等位基因在栽培大豆中都存在。ASLP位点的等位基因多样性值接近先前对限制性片段长度多态性的估计,因此ASLP可能作为定点作图中的遗传标记有用。