Maslov D A, Kolesnikov A A, Zaitseva G N
Mol Biochem Parasitol. 1984 Jul;12(3):351-64. doi: 10.1016/0166-6851(84)90091-4.
The structure of kinetoplast maxicircle DNA from trypanosomatids Crithidia oncopelti, C. luciliae, Leptomonas pessoai and Leishmania gymnodactyli was compared by the blot hybridization method. The sizes of these molecules are 24.5, 34, 31 and 38 kilobase pairs (kbp), respectively. Labelled maxicircle fragments from C. oncopelti were used as probes. A general model of the structural organization of maxicircles is proposed according to which this molecule is composed of a 17kbp conservative region and a divergent one occupying the rest of the molecule. The conservative region contains the sequences homologous to those in all trypanosomatids. The sequence of the divergent region exhibits no cross homology detectable by high stringency hybridization. The main size differences between the maxicircle molecules from different trypanosomatid species are explained by the length variability of their divergent regions.
通过印迹杂交法比较了锥虫科昆虫克氏锥虫、绿蝇锥虫、佩氏利什曼原虫和裸指利什曼原虫动质体大环DNA的结构。这些分子的大小分别为24.5、34、31和38千碱基对(kbp)。来自克氏锥虫的标记大环片段用作探针。提出了大环结构组织的一般模型,根据该模型,该分子由一个17kbp的保守区域和一个占据分子其余部分的发散区域组成。保守区域包含与所有锥虫中序列同源的序列。发散区域的序列在高严谨度杂交下未显示可检测到的交叉同源性。不同锥虫物种的大环分子之间的主要大小差异是由其发散区域的长度变异性解释的。