Molecular Ecology, Institute for Environmental Sciences, University Koblenz-Landau, Fortstr. 7, 76829 Landau, Germany.
Mol Ecol Resour. 2012 Jul;12(4):697-705. doi: 10.1111/j.1755-0998.2012.03142.x. Epub 2012 Apr 5.
Microsatellite markers are important tools in population, conservation and forensic studies and are frequently used for species delineation, the detection of hybridization and introgression. Therefore, marker sets that amplify variable DNA regions in two species are required; however, cross-species amplification is often difficult, as genotyping errors such as null alleles may occur. To estimate the level of potential misidentifications based on genotyping errors, we compared the occurrence of parental alleles in laboratory and natural Daphnia hybrids (Daphnia longispina group). We tested a set of 12 microsatellite loci with regard to their suitability for unambiguous species and hybrid class identification using F(1) hybrids bred in the laboratory. Further, a large set of 44 natural populations of D. cucullata, D. galeata and D. longispina (1715 individuals) as well as their interspecific hybrids were genotyped to validate the discriminatory power of different marker combinations. Species delineation using microsatellite multilocus genotypes produced reliable results for all three studied species using assignment tests. Daphnia galeata × cucullata hybrid detection was limited due to three loci exhibiting D. cucullata-specific null alleles, which most likely are caused by differences in primer-binding sites of parental species. Overall, discriminatory power in hybrid detection was improved when a subset of markers was identified that amplifies equally well in both species.
微卫星标记是种群、保护和法医学研究中的重要工具,常用于物种划分、杂交和渐渗的检测。因此,需要标记集来扩增两个物种中可变的 DNA 区域;然而,跨物种扩增通常很困难,因为可能会出现基因型错误,如无效等位基因。为了根据基因型错误估计潜在误识别的程度,我们比较了实验室和自然条件下的 Daphnia 杂种(长额溞组)中亲代等位基因的发生情况。我们使用实验室培育的 F1 杂种,测试了一组 12 个微卫星位点,以确定它们是否适合明确物种和杂种类别的鉴定。此外,对 44 个自然种群的 D. cucullata、D. galeata 和 D. longispina(1715 个个体)及其种间杂种进行了大规模基因分型,以验证不同标记组合的区分能力。使用微卫星多位点基因型进行物种划分,使用分配测试对所有三种研究物种产生了可靠的结果。由于三个位点表现出 D. cucullata 特异性无效等位基因,D. galeata × cucullata 杂种的检测受到限制,这些无效等位基因很可能是由于亲本物种的引物结合位点不同引起的。总的来说,当确定一组在两个物种中扩增效果相同的标记子集时,杂种检测的区分能力得到了提高。