Landergott Urs, Naciri Yamama, Schneller J Jakob, Holderegger Rolf
Institute of Systematic Botany, University of Zurich, Zollikerstrasse 107, 8008, Zurich, Switzerland.
Theor Appl Genet. 2006 Aug;113(3):453-65. doi: 10.1007/s00122-006-0310-6. Epub 2006 Jun 20.
Polyploidy plays a pivotal role in plant evolution. However, polyploids with polysomic inheritance have hitherto been severely underrepresented in plant population genetic studies, mainly due to a lack of appropriate molecular genetic markers. Here we report the establishment and experimental validation of six fully informative microsatellite markers in tetraploid gynodioecious Thymus praecox agg. Sequence data of 150 microsatellite alleles and their flanking regions revealed high variation, which may be characteristic for polyploids with a reticulate evolutionary history. Understanding the patterns of mutation (indels and substitutions) in microsatellite flanking-sequences was a prerequisite for the development of co-dominant markers for fragment analyses. Allelic segregation patterns among progeny arrays from ten test crosses revealed tetrasomic inheritance in T. praecox agg. No evidence of frequent double reduction was detected. Polymerase chain reaction (PCR) based dosage effects allowed for precise assignment of allelic configuration at all six microsatellite loci. The quantification of allele copy numbers in PCR was verified by comparisons of observed and expected gametic allele frequencies and heterozygosities in test crosses. Our study illustrates how PCR based markers can provide reliable estimates of heterozygosity and, thus, powerful tools for breeding system and population genetic analyses in polyploid organisms.
多倍体在植物进化中起着关键作用。然而,具有多体遗传的多倍体在植物群体遗传学研究中一直严重缺乏代表性,主要原因是缺乏合适的分子遗传标记。在此,我们报告了在四倍体雌雄异株的早花百里香复合体中六个完全信息性微卫星标记的建立及实验验证。150个微卫星等位基因及其侧翼区域的序列数据显示出高度变异,这可能是具有网状进化历史的多倍体的特征。了解微卫星侧翼序列中的突变模式(插入缺失和替换)是开发用于片段分析的共显性标记的先决条件。来自十个测交的子代阵列中的等位基因分离模式显示早花百里香复合体中存在四体遗传。未检测到频繁双减数的证据。基于聚合酶链反应(PCR)的剂量效应允许在所有六个微卫星位点精确确定等位基因构型。通过比较测交中观察到的和预期的配子等位基因频率及杂合度,验证了PCR中等位基因拷贝数的定量。我们的研究说明了基于PCR的标记如何能够提供可靠的杂合度估计,从而为多倍体生物的育种系统和群体遗传学分析提供强大工具。