Macina R A, Sanchez D O, Affranchino J L, Engel J C, Frasch A C
Mol Biochem Parasitol. 1985 Jun;16(1):61-74. doi: 10.1016/0166-6851(85)90049-0.
Four minicircle classes were analyzed using cloned minicircles as probes and single-cell cloned Trypanosoma cruzi parasites. The hybridization conditions used allowed identification of minicircle classes within kinetoplast DNA that were non-homologous to each other. Two of these minicircle classes, detected with probes pTckAWP-2 and -3, were present together in several of the CA 1 and Miranda clones, in spite of the fact that either pTckAWP-2 or both minicircle classes were undetectable in other isolates and clones of the parasite. The other two minicircle classes (pTckM-84 and -88) were located in some Miranda cloned parasites which were characterized by the simple restriction endonuclease pattern of their minicircles. Both pTckM-84 and -88 minicircle classes represented 52-71% of the kinetoplast DNA in the latter group of trypanosomes. Restriction endonuclease mapping allowed the identification of polymorphic minicircles in two of the four minicircle classes analyzed (pTckAWP-2 and pTckM-88). The polymorphisms were observed in part of the molecules of one minicircle class within a single trypanosome clone, as well as when different clones or even some of those obtained from the same isolate were compared. In addition, a different proportion of pTckM-88 type of minicircle sequence class was observed in the kinetoplast DNA from two of the Miranda clones analyzed. These observations demonstrated that similar molecules may evolve independently in sequence in each parasite. The polymorphic minicircles detected may arise from sequence variations before expansion of a future homogeneous minicircle sequence class.
使用克隆的微小环作为探针和单细胞克隆的克氏锥虫寄生虫,对四个微小环类别进行了分析。所使用的杂交条件能够鉴定动质体DNA中彼此非同源的微小环类别。尽管在该寄生虫的其他分离株和克隆中,探针pTckAWP - 2或这两个微小环类别均无法检测到,但用探针pTckAWP - 2和 - 3检测到的这两个微小环类别,在几个CA 1和米兰达克隆中同时存在。另外两个微小环类别(pTckM - 84和 - 88)存在于一些米兰达克隆的寄生虫中,这些寄生虫的特征是其微小环具有简单的限制性内切酶图谱。在后者的锥虫组中,pTckM - 84和 - 88微小环类别均占动质体DNA的52 - 71%。限制性内切酶图谱分析使得能够在分析的四个微小环类别中的两个(pTckAWP - 2和pTckM - 88)中鉴定出多态性微小环。在单个锥虫克隆内的一个微小环类别的部分分子中观察到了多态性,并且在比较不同克隆甚至从同一分离株获得的一些克隆时也观察到了多态性。此外,在分析的两个米兰达克隆的动质体DNA中,观察到pTckM - 88型微小环序列类别的比例不同。这些观察结果表明,相似的分子可能在每个寄生虫中独立地进行序列进化。检测到的多态性微小环可能源于未来均匀微小环序列类别扩增之前的序列变异。