Gotoh O, Hayashi J I, Yonekawa H, Tagashira Y
J Mol Evol. 1979 Dec;14(4):301-10. doi: 10.1007/BF01732497.
We have developed a theory to estimate the degree of sequence divergence between related DNAs from the comparison of restriction endonuclease recognition sites. Two major improvements have been made upon a similar method reported by Upholt (1977). First, the most probable value is calculated by the collective use of all available data. This reduces intrinsic statistical error and extends the analyzable range of sequence divergence. Second, all variables are redefined so that they have strict mathematical implications. This corrects a serious error arising from the misinterpretation of the meaning of the fraction of conserved cleavage sites. With this refined method, sequence divergence between rat and mouse mitochondrial DNAs (mtDNAs) was calculated to be about 25% substitutions/nucleotide, which is in good agreement with the DNA-DNA hybridization data obtained by Jakovcic et al. (1975). It was also estimated that the three types of rat mtDNAs differ from one another by 0.3 approximately 1% of total base pairs. These values are 2 approximately 5 times smaller than those obtained with the conventional method.
我们已经开发出一种理论,可通过比较限制性内切核酸酶识别位点来估计相关DNA之间的序列差异程度。在Upholt(1977年)报道的类似方法基础上有两项主要改进。首先,通过综合使用所有可用数据来计算最可能值。这减少了内在统计误差,并扩展了序列差异的可分析范围。其次,对所有变量进行重新定义,使其具有严格的数学含义。这纠正了因对保守切割位点分数含义的错误解读而产生的严重误差。使用这种改进方法,计算出大鼠和小鼠线粒体DNA(mtDNA)之间的序列差异约为25%替换/核苷酸,这与Jakovcic等人(1975年)获得的DNA-DNA杂交数据高度一致。还估计出三种类型的大鼠mtDNA彼此之间相差约0.3%至1%的总碱基对。这些值比用传统方法获得的值小2至5倍。