Suzuki Y, Gojobori T
Center for Information Biology, National Institute of Genetics, Mishima, Japan.
Mol Biol Evol. 1997 Aug;14(8):800-6. doi: 10.1093/oxfordjournals.molbev.a025820.
Molecular evolutionary analyses for Ebola and Marburg viruses were conducted with the aim of elucidating evolutionary features of these viruses. In particular, the rate of nonsynonymous substitutions for the glycoprotein gene of Ebola virus was estimated to be, on the average, 3.6 x 10(-5) per site per year. Marburg virus was also suggested to be evolving at a similar rate. Those rates were a hundred times slower than those of retroviruses and human influenza A virus, but were of the same order of magnitude as that of the hepatitis B virus. When these rates were applied to the degree of sequence divergence, the divergence time between Ebola and Marburg viruses was estimated to be more than several thousand years ago. Moreover, most of the nucleotide substitutions were transitions and synonymous for Marburg virus. This suggests that purifying selection has operated on Marburg virus during evolution.
为阐明埃博拉病毒和马尔堡病毒的进化特征,开展了针对这两种病毒的分子进化分析。特别是,埃博拉病毒糖蛋白基因的非同义替换率估计平均每年每个位点为3.6×10⁻⁵。马尔堡病毒也被认为以类似的速率进化。这些速率比逆转录病毒和甲型人流感病毒慢一百倍,但与乙型肝炎病毒处于同一数量级。当将这些速率应用于序列分歧程度时,估计埃博拉病毒和马尔堡病毒之间的分歧时间超过几千年前。此外,马尔堡病毒的大多数核苷酸替换是转换和同义的。这表明在进化过程中纯化选择作用于马尔堡病毒。