Mizokami M, Orito E, Ohba K, Ikeo K, Lau J Y, Gojobori T
Second Department of Medicine, Nagoya City University Medical School, Japan.
J Mol Evol. 1997;44 Suppl 1:S83-90. doi: 10.1007/pl00000061.
With the aim of elucidating the evolution of a hepadnavirus family, we constructed molecular phylogenetic trees for 27 strains of hepatitis B virus (HBV) using both the unweighted pair-grouping and neighbor-joining methods. All five gene regions, P, C, S, X, and preS, were used to construct the phylogenetic trees. Using the phylogenetic trees obtained, we classified these strains into five major groups in which the strains were closely related to each other. Our classification reinforced our previous view that genetic classification is not always compatible with conventional classification determined by serological subtypes. Moreover, constraints on the evolutionary process of HBV were analyzed for amino-acid-altering (nonsynonymous) and silent (synonymous) substitutions, because two-thirds of the open reading frame (ORF), P, contains alternating overlapping ORFs. In our unique analysis of this interesting gene structure of HBV, the most frequent synonymous substitutions were observed in the nonoverlapped parts of the P and C genes. On the other hand, the number of synonymous substitutions per nucleotide site for the S gene was quite low and appeared a strongly constrained evolution. Because the P gene overlaps the S gene in a different frame, the low rate of synonymous substitution for the S gene can be explained by the evolutionary constraints which are imposed on the overlapping gene region. In other words, synonymous substitutions in the S gene can cause amino acid changes in its overlapping region in a different frame. Thus, the evolution of HBV is constrained evolutionarily by the overlapping genes. We propose calling this mode of viral evolution "constrained evolution." The evolution of HBV represents a typical constrained evolution.
为了阐明嗜肝DNA病毒科的进化过程,我们使用非加权配对分组法和邻接法构建了27株乙型肝炎病毒(HBV)的分子系统发育树。所有五个基因区域,即P、C、S、X和前S基因区域,均用于构建系统发育树。利用得到的系统发育树,我们将这些菌株分为五个主要组,组内菌株彼此密切相关。我们的分类强化了我们之前的观点,即基因分类并不总是与血清学亚型确定的传统分类相一致。此外,还分析了HBV进化过程中氨基酸改变(非同义)和沉默(同义)替换的限制因素,因为开放阅读框(ORF)的三分之二,即P基因,包含交替重叠的ORF。在我们对HBV这种有趣基因结构的独特分析中,同义替换最常出现在P基因和C基因的非重叠部分。另一方面,S基因每个核苷酸位点的同义替换数量相当低,呈现出强烈的进化限制。由于P基因与S基因以不同的阅读框重叠,S基因同义替换率低可以用重叠基因区域所施加的进化限制来解释。换句话说,S基因中的同义替换可能会在不同阅读框的重叠区域导致氨基酸变化。因此,HBV的进化在进化上受到重叠基因的限制。我们建议将这种病毒进化模式称为“受限进化”。HBV的进化代表了一种典型的受限进化。