Grassly N C, Holmes E C
Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, U.K.
Mol Biol Evol. 1997 Mar;14(3):239-47. doi: 10.1093/oxfordjournals.molbev.a025760.
Different regions along nucleotide sequences are often subject to different evolutionary forces. Recombination will result in regions having different evolutionary histories, while selection can cause regions to evolve at different rates. This paper presents a statistical method based on likelihood for detecting such processes by identifying the regions which do not fit with a single phylogenetic topology and nucleotide substitution process along the entire sequence. Subsequent reanalysis of these anomalous regions may then be possible. The method is tested using simulations, and its application is demonstrated using the primate psi eta-globin pseudogene, the V3 region of the envelope gene of HIV-1, and argF sequences from Neisseria bacteria. Reanalysis of anomalous regions is shown to reveal possible immune selection in HIV-1 and recombination in Neisseria. A computer program which implements the method is available.
核苷酸序列上的不同区域通常受到不同的进化力量影响。重组会导致各区域具有不同的进化历史,而选择则会使不同区域以不同速率进化。本文提出了一种基于似然性的统计方法,通过识别那些不符合单一系统发育拓扑结构以及沿整个序列的核苷酸替换过程的区域,来检测此类过程。随后对这些异常区域进行重新分析便成为可能。该方法通过模拟进行了测试,并使用灵长类ψη - 珠蛋白假基因、HIV - 1包膜基因的V3区域以及奈瑟氏菌属细菌的argF序列展示了其应用。对异常区域的重新分析表明,HIV - 1中可能存在免疫选择,而奈瑟氏菌属中存在重组现象。有一个实现该方法的计算机程序可供使用。