Nei M, Tajima F
Center for Demographic and Population Genetics, University of Texas, Houston 77225.
Mol Biol Evol. 1985 May;2(3):189-205. doi: 10.1093/oxfordjournals.molbev.a040345.
A mathematical theory for the evolutionary change of restriction endonuclease cleavage sites is developed, and the probabilities of various types of restriction-site changes are evaluated. A computer simulation is also conducted to study properties of the evolutionary change of restriction sites. These studies indicate that parsimony methods of constructing phylogenetic trees often make erroneous inferences about evolutionary changes of restriction sites unless the number of nucleotide substitutions per site is less than 0.01 for all branches of the tree. This introduces a systematic error in estimating the number of mutational changes for each branch and, consequently, in constructing phylogenetic trees. Therefore, parsimony methods should be used only in cases where nucleotide sequences are closely related. Reexamination of Ferris et al.'s data on restriction-site differences of mitochondrial DNAs does not support Templeton's conclusions regarding the phylogenetic tree for man and apes and the molecular clock hypothesis. Templeton's claim that Nei and Li's method of estimating the number of nucleotide substitutions per site is seriously affected by parallel losses and loss-gains of restriction sites is also unsupported.
本文建立了一种关于限制性内切酶切割位点进化变化的数学理论,并评估了各类限制性位点变化的概率。同时进行了计算机模拟以研究限制性位点进化变化的特性。这些研究表明,构建系统发育树的简约法常常会对限制性位点的进化变化做出错误推断,除非树的所有分支每个位点的核苷酸替换数小于0.01。这在估计每个分支的突变变化数量时引入了系统误差,进而在构建系统发育树时也产生误差。因此,简约法仅应在核苷酸序列密切相关的情况下使用。对费里斯等人关于线粒体DNA限制性位点差异的数据重新审视后发现,并不支持邓普顿关于人类和猿类系统发育树以及分子钟假说的结论。邓普顿声称内和李估计每个位点核苷酸替换数的方法会受到限制性位点平行丢失和得失的严重影响,这一说法也未得到支持。