Sanchez D O, Frasch A C, Carrasco A E, Gonzalez-Cappa S M, de Isola E D, Stoppani A O
Mol Biochem Parasitol. 1984 Apr;11:169-78. doi: 10.1016/0166-6851(84)90063-x.
Nine Trypanosoma cruzi isolates not examined previously for kDNA structure were characterized by (a) endonuclease restriction analysis of mini-circles, followed by agarose gel-electrophoresis of digests, and (b) hybridization of mini- and maxi-circle fragments with four 32P-labeled cloned mini-circles from T. cruzi (pTck-1, 12, 13 and 14) or with 32P-labeled maxi-circles from T. brucei, respectively. The gel electrophoresis patterns demonstrated significant differences between isolates, which were confirmed and extended by the hybridization assay. When using pTck-1 and pTck-12 as probes, widely distributed heterogeneous mini-circle subpopulations were demonstrated in all the examined isolates, despite the occurrence of extensive homologies. pTck-14, assayed under high stringent conditions, detected an almost homogeneous mini-circle subpopulation in only three isolates, although under relaxed conditions, pTck-14 shared sequence homologies with most of the mini-circle subpopulations from all isolates. Rapidly evolving mini-circle regions were also detected using as probe pTck-13, a small mini-circle fragment. Preliminary maxi-circle characterization revealed polymorphic restriction endonuclease sites in the different T. cruzi isolates. These results were consistent with those obtained with mini-circles subjected to the same treatment.
对9株之前未检测过kDNA结构的克氏锥虫分离株进行了如下鉴定:(a) 对微小环进行核酸内切酶限制分析,然后对酶切产物进行琼脂糖凝胶电泳;(b) 分别用来自克氏锥虫的4个32P标记的克隆微小环(pTck-1、12、13和14)或来自布氏锥虫的32P标记的大环与微小环和大环片段进行杂交。凝胶电泳图谱显示各分离株之间存在显著差异,杂交试验证实并扩展了这些差异。当使用pTck-1和pTck-12作为探针时,尽管存在广泛的同源性,但在所有检测的分离株中均显示出广泛分布的异质微小环亚群。在高严格条件下检测时,pTck-14仅在3株分离株中检测到几乎同质的微小环亚群,不过在宽松条件下,pTck-14与所有分离株的大多数微小环亚群具有序列同源性。使用小的微小环片段pTck-13作为探针也检测到了快速进化的微小环区域。对大环的初步鉴定揭示了不同克氏锥虫分离株中多态性的限制性核酸内切酶位点。这些结果与对经过相同处理的微小环所获得的结果一致。