Sueoka N
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309-0347.
J Mol Evol. 1995 Mar;40(3):318-25. doi: 10.1007/BF00163236.
When there are no biases in mutation and selection between the two strands of DNA, the 12 possible substitution rates of the four nucleotides reduces to six (type 1 parity rule or PR1), and the intrastrand average base composition is expected to be A = T and G = C at equilibrium without regard to the G + C content of DNA (type 2 parity rule or PR2). Significant deviations from the parity rules in the third codon letters of the four-codon amino acids result mostly from selective biases rather than mutational biases between the two strands of DNA during evolution. The parity rules lay the foundation for evaluating the biases in synonymous codon usage in terms of (1) directional mutation pressure for variation of the DNA G + C content due to mutational biases between alpha-bases (A or T) and gamma-bases (G or C), (2) strand-bias mutation, for example, by DNA repair during transcription, and (3) functional selection in evolution, for example, due to tRNA abundance. The present analysis shows that, although the PR2 violation is common in the third codon letters of four-codon amino acids, the contribution of PR2 violation to the DNA G + C content of the third codon position is small and, in majority of cases, mildly counteracts the effect of the directional mutation pressure on the G + C content.
当DNA的两条链在突变和选择上不存在偏差时,四种核苷酸的12种可能的替换率会简化为六种(1型奇偶规则或PR1),并且在平衡状态下,链内平均碱基组成预期为A = T且G = C,而与DNA的G + C含量无关(2型奇偶规则或PR2)。在四个密码子的氨基酸的第三个密码子字母中,与奇偶规则的显著偏差主要源于进化过程中DNA两条链之间的选择偏差而非突变偏差。奇偶规则为从以下方面评估同义密码子使用偏差奠定了基础:(1)由于α碱基(A或T)和γ碱基(G或C)之间的突变偏差导致的DNA G + C含量变化的定向突变压力;(2)链偏性突变,例如转录过程中的DNA修复;(3)进化中的功能选择,例如由于tRNA丰度。目前的分析表明,虽然在四个密码子的氨基酸的第三个密码子字母中违反PR2的情况很常见,但违反PR2对第三个密码子位置的DNA G + C含量的贡献很小,并且在大多数情况下,会轻微抵消定向突变压力对G + C含量的影响。