Fitch W M
J Mol Evol. 1976 Jun 23;8(1):13-40. doi: 10.1007/BF01738880.
Using many more cytochrome sequences than previously available, we have confirmed: 1, the eukaryotic cytochrome c diverged from a common ancestor; 2, the ancestral eukaryotic cytochrome c was not greatly different in character from those present today; 3, fixations are non-randomly distributed among the codons, there being evidence for at least four classes of variability; 4, there are similar classes of variability when the data are considered according to the nucleotide position within the codon; 5, the number of covarions (concomitantly variable codons) in mammalian cytochrome c genes is about 12 and the same value has been obtained for dicotyledenous plants as well; 6, all of the hyper- and most highly variable codons are for external residues, nearly 60 per cent of the invariable codons are for internal residues and nearly half of the codons for internal residues are invariable; 7, the first nucleotide position of a codon is more likely and the second position less likely to fix mutations than would be expected on the basis of the number of ways that alternative amino acids can be reached; 8, the character of nucleotide replacements is enormously non-random, with G-A interchanges representing 42% of those observed in the first nucleotide position, but the observation does not stem from a bias in the DNA strand receiving the mutation, nor from the presence of a compositional equilibrium, nor from a bias in the frequency with which different nucleotides mutate, but rather from a bias in the acceptability of an alternative nucleotide as circumscribed by the functional acceptability of the new amino acid encoded; and 9, the unit evolutionary period is approximately 150 million years/observable (amino acid changing) nucleotide replacement/cytochrome c covarion in two diverging lines. Wherever non-randomness has been observed, it has always been consistent with the consideration that an alternative amino acid at any location is more likely to be acceptable the more closely it resembles the present amino acid in its physico-chemical properties. Finally, in no case did the a priori assumption of a biologically realistic phylogeny lead to any observations or conclusions that were in any way significantly different from those obtained when the phylogeny was based solely upon the sequences, proving that the earlier results were not a consequence of some internal circularity.
我们使用了比以往更多的细胞色素序列,证实了以下几点:1. 真核生物的细胞色素c源自一个共同祖先;2. 原始真核生物细胞色素c在特性上与当今的细胞色素c没有太大差异;3. 固定在密码子间的分布是非随机的,至少有四类变异性的证据;4. 根据密码子内的核苷酸位置考虑数据时,存在类似的变异性类别;5. 哺乳动物细胞色素c基因中的协变子(伴随可变密码子)数量约为12个,双子叶植物也得到了相同的值;6. 所有高度可变和最可变的密码子对应外部残基,近60%的不变密码子对应内部残基,近一半的内部残基密码子是不变的;7. 密码子的第一个核苷酸位置比基于可达到替代氨基酸的方式数量所预期的更有可能固定突变,而第二个位置则不太可能;8. 核苷酸替换的特征极大地非随机,G-A互换占在第一个核苷酸位置观察到的替换的42%,但这一观察结果并非源于接受突变的DNA链中的偏差,也不是由于组成平衡的存在,也不是由于不同核苷酸突变频率的偏差,而是源于新编码氨基酸的功能可接受性所限定的替代核苷酸的可接受性偏差;9. 在两条分歧谱系中,单位进化期约为1.5亿年/可观察到的(氨基酸变化的)核苷酸替换/细胞色素c协变子。无论何处观察到非随机性,它总是与这样的考虑一致,即任何位置的替代氨基酸在物理化学性质上与当前氨基酸越相似,就越有可能被接受。最后,在任何情况下,基于生物学现实系统发育的先验假设都没有导致任何与仅基于序列获得的观察结果或结论有任何显著差异的结果,证明早期结果不是某种内部循环的结果。