Pearce John M
Institute of Arctic Biology and Department of Biology and Wildlife, University of Alaska, Fairbanks, AK 99775, USA.
Mol Ecol. 2006 Feb;15(2):333-41. doi: 10.1111/j.1365-294X.2005.02781.x.
Insertions and deletions (indels) result in sequences of various lengths when homologous gene regions are compared among individuals or species. Although indels are typically phylogenetically informative, occurrence and incorporation of these characters as gaps in intraspecific population genetic data sets are rarely discussed. Moreover, the impact of gaps on estimates of fixation indices, such as F(ST), has not been reviewed. Here, I summarize the occurrence and population genetic signal of indels among 60 published studies that involved alignments of multiple sequences from the mitochondrial DNA (mtDNA) control region of vertebrate taxa. Among 30 studies observing indels, an average of 12% of both variable and parsimony-informative sites were composed of these sites. There was no consistent trend between levels of population differentiation and the number of gap characters in a data block. Across all studies, the average influence on estimates of PhiST was small, explaining only an additional 1.8% of among population variance (range 0.0-8.0%). Studies most likely to observe an increase in PhiST with the inclusion of gap characters were those with < 20 variable sites, but a near equal number of studies with few variable sites did not show an increase. In contrast to studies at interspecific levels, the influence of indels for intraspecific population genetic analyses of control region DNA appears small, dependent upon total number of variable sites in the data block, and related to species-specific characteristics and the spatial distribution of mtDNA lineages that contain indels.
当在个体或物种之间比较同源基因区域时,插入和缺失(indels)会导致不同长度的序列。尽管indels通常具有系统发育信息,但在种内群体遗传数据集中,这些特征作为间隙的出现和纳入却很少被讨论。此外,间隙对固定指数估计值(如F(ST))的影响也尚未得到综述。在这里,我总结了60项已发表研究中indels的出现情况和群体遗传信号,这些研究涉及脊椎动物类群线粒体DNA(mtDNA)控制区多个序列的比对。在30项观察到indels的研究中,可变位点和简约信息位点平均有12%由这些位点组成。数据块中的群体分化水平与间隙特征数量之间没有一致的趋势。在所有研究中,间隙对PhiST估计值的平均影响较小,仅额外解释了群体间方差的1.8%(范围为0.0 - 8.0%)。最有可能因纳入间隙特征而观察到PhiST增加的研究是那些可变位点少于20个的研究,但可变位点较少的研究中,几乎有同样数量的研究并未显示出增加。与种间水平的研究不同,indels对控制区DNA种内群体遗传分析的影响似乎较小,这取决于数据块中可变位点的总数,并与物种特异性特征以及包含indels的mtDNA谱系的空间分布有关。