Shepherd L D, Lambert D M
Allan Wilson Centre for Molecular Ecology and Evolution, Institute of Molecular BioSciences, Massey University, Private Bag 102904, North Shore Mail Centre, Auckland, New Zealand.
J Hered. 2005 Sep-Oct;96(5):566-71. doi: 10.1093/jhered/esi070. Epub 2005 Jul 1.
Analysis of nucleotide sequence variation at a microsatellite DNA locus revealed extensive size homoplasy of alleles in Adélie penguins (Pygoscelis adeliae). Variation in the flanking regions at this locus allowed discrimination between mechanisms proposed for length changes in microsatellite DNA alleles. We further examined the structure of alleles for the same microsatellite DNA locus across 11 additional species of penguin (Spheniscidae) by mapping allele sequences onto an independent penguin phylogeny. Our analysis indicated that the repeat motifs appear to have evolved independently on several occasions. We observed sequence instability in the region bordering the repeat tract with a transversional bias predominating. We propose that this bias results from inaccurate DNA replication owing to the sequence context of this repeat tract. Because we show that regions flanking repeat sequences exhibit this mutational bias, this cautions against the use of such regions for phylogeny reconstruction.
对一个微卫星DNA位点的核苷酸序列变异分析揭示了阿德利企鹅(阿德利企鹅属)等位基因广泛的大小同塑性。该位点侧翼区域的变异使得我们能够区分微卫星DNA等位基因长度变化所提出的机制。我们通过将等位基因序列映射到一个独立的企鹅系统发育树上,进一步研究了另外11种企鹅(企鹅科)中相同微卫星DNA位点的等位基因结构。我们的分析表明,重复基序似乎在多个场合独立进化。我们观察到重复序列边界区域的序列不稳定,其中转换偏向占主导。我们认为这种偏向是由于该重复序列的序列背景导致DNA复制不准确所致。因为我们表明重复序列侧翼区域表现出这种突变偏向,这提醒我们在系统发育重建中不要使用这些区域。