Lipman D J, Wilbur W J
J Mol Biol. 1983 Jan 25;163(3):363-76. doi: 10.1016/0022-2836(83)90063-3.
We have studied the statistical constraints on synonymous codon choice to evaluate various proposals regarding the origin of the bias in synonymous codon usage observed by Fiers et al. (1975), Air et al. (1976), Grantham et al. (1980) and others. We have determined the statistical dependence of the degenerate third base on either of its nearest neighbors in mitochondrial, prokaryotic, and eukaryotic coding sequences. We noted an increasing dependence of the third base on its nearest neighbors in moving from mitochondria to prokaryotes to eukaryotes. A statistical model assuming random equiprobable selection of synonymous codons was found grossly adequate for the mitochondria, but totally inadequate for prokaryotes and eukaryotes. A model assuming selection of synonymous codons reflecting a genomic strategy, i.e. the genome hypothesis of Grantham et al. (1980), gave a good approximation of the mitochondrial sequences. A statistical model which exactly maintains codon frequency, but allows the position of corresponding synonymous codons to vary was only grossly adequate for prokaryotes and totally inadequate for eukaryotes. The results of these simulations are consistent with the measures on experimental sequences and suggest that a "frequency constraint" model such as that of Grantham et al. (1980) may be an adequate explanation of the codon usage in mitochondria. However, in addition to this frequency constraint, there may be constraints on synonymous codon choice in prokaryotes due to codon context. Furthermore, any proposal to explain codon usage in eukaryotes must involve a constraint on the context of a codon in the sequence.
我们研究了同义密码子选择的统计限制,以评估关于菲尔斯等人(1975年)、艾尔等人(1976年)、格兰瑟姆等人(1980年)及其他研究者所观察到的同义密码子使用偏好起源的各种提议。我们确定了线粒体、原核生物和真核生物编码序列中简并的第三位碱基与其任一相邻碱基之间的统计依赖性。我们注意到,从线粒体到原核生物再到真核生物,第三位碱基对其相邻碱基的依赖性逐渐增加。一个假设同义密码子随机等概率选择的统计模型被发现对线粒体来说大致适用,但对原核生物和真核生物则完全不适用。一个假设同义密码子选择反映基因组策略的模型,即格兰瑟姆等人(1980年)的基因组假说,对线粒体序列给出了较好的近似。一个精确维持密码子频率,但允许相应同义密码子位置变化的统计模型对原核生物只是大致适用,对真核生物则完全不适用。这些模拟结果与对实验序列的测量结果一致,并表明像格兰瑟姆等人(1980年)提出的那种“频率限制”模型可能是对线粒体密码子使用的一个充分解释。然而,除了这种频率限制外,原核生物中同义密码子的选择可能还受到密码子上下文的限制。此外,任何解释真核生物密码子使用的提议都必须涉及对序列中密码子上下文的限制。