American Museum of Natural History, Division of Invertebrate Zoology, Central Park West at 79th St., New York City, NY 10024, USA.
Mol Phylogenet Evol. 2013 Sep;68(3):471-81. doi: 10.1016/j.ympev.2013.04.025. Epub 2013 May 10.
Identification of paralogy in candidate nuclear loci is an important prerequisite in phylogenetics and statistical phylogeography, but one that is often overlooked. One marker commonly assumed to be a single-copy gene and claimed to harbor great utility for inferring recent divergences is elongation factor-1α (EF-1α). To test this hypothesis, we systematically cloned EF-1α in three disjunct populations of the harvestman Metasiro americanus. Here we show that EF-1α has a large number of paralogs in this species. The paralogs do not evolve in a concerted manner, and the paralogs diverged prior to the population divergence. Moreover, the paralogs of M. americanus are not comparable to the highly divergent EF-1α paralogs found in bees and spiders, which are easily recognized and separated through the use of specific primers. We demonstrate statistically that our detection of paralogs cannot be attributed to amplification error. The presence of EF-1α paralogs in M. americanus prevents its use in statistical phylogeography, and the presence of out-paralogs argues against its use in phylogenetic inference among recently diverged clades. These data contradict the common assumption that EF-1α is for most or all taxa a single-copy gene, or that it has a small number of paralogs that are homogenized through gene conversion, unequal crossing over, or other processes.
在系统发育学和统计系统地理学中,鉴定直系同源基因是一个重要的前提条件,但往往被忽视。一个通常被认为是单拷贝基因的标记,被认为对推断近期分化具有很大的作用,这个标记就是延伸因子-1α(EF-1α)。为了检验这个假设,我们在三种不同的 harvestman Metasiro americanus 种群中系统地克隆了 EF-1α。在这里,我们表明 EF-1α在这个物种中有大量的直系同源基因。这些直系同源基因没有协同进化,而且在种群分化之前就已经分化了。此外,M. americanus 的直系同源基因与在蜜蜂和蜘蛛中发现的高度分化的 EF-1α 直系同源基因不同,后者可以通过使用特定的引物很容易地识别和分离。我们通过统计学证明,我们检测到的直系同源基因不能归因于扩增错误。EF-1α 直系同源基因的存在使得它不能用于统计系统地理学,而外源性直系同源基因的存在则反对其在最近分化的类群中的系统发育推断中使用。这些数据与 EF-1α 对于大多数或所有分类群是单拷贝基因的常见假设相矛盾,或者它只有少数通过基因转换、不等交换或其他过程均匀化的直系同源基因。