首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Karyotype variability in KP1(+) and KP1(-) strains of Trypanosoma rangeli isolated in Brazil and Colombia.
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Karyotype variability in KP1(+) and KP1(-) strains of Trypanosoma rangeli isolated in Brazil and Colombia.

机译:在巴西和哥伦比亚分离的锥虫锥虫KP1(+)和KP1(-)菌株的核型变异。

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In the present study, the molecular karyotypes of 12 KP1(+) and KP1(-) Trypanosoma rangeli strains were determined and 10 different molecular markers were hybridized to the chromosomes of the parasite, including seven obtained from T. rangeli [ubiquitin hydrolase (UH), a predicted serine/threonine protein kinase (STK), hexose transporter, hypothetical protein, three anonymous sequences] and three from Trypanosoma cruzi [ubiquitin-conjugating enzyme E2 (UBE2), ribosomal RNA methyltransferase (rRNAmtr), proteasome non-ATPase regulatory subunit 6 (PSMD6)]. Despite intraspecific variation, analysis of the karyotype profiles permitted the division of the T. rangeli strains into two groups coinciding with the KP1(+) and KP1(-) genotypes. Southern blot hybridization showed that, except for the hexose transporter probe, all other probes produced distinct patterns able to differentiate the KP1(+) and KP1(-) genotypes. The UH, STK and An-1A04 probes exclusively hybridized to the chromosomes of KP1(+) strains andcan be used as markers of this group. In addition, the UBE2, rRNAmtr and PSMD6 markers, which are present in a conserved region in all trypanosomatid species sequenced so far, co-hybridized to the same T. rangeli chromosomal bands, suggesting the occurrence of gene synteny in these species. The finding of distinct molecular karyotypes in KP1(+) and KP1(-) strains of T. rangeli is noteworthy and might be used as a new approach to the study of genetic variability in this parasite. Together with the Southern blot hybridization results, these findings demonstrate that differences at the kDNA level might be associated with variations in nuclear DNA.
机译:在本研究中,确定了12个KP1(+)和KP1(-)锥虫锥虫菌株的分子核型,并将10种不同的分子标记杂交到该寄生虫的染色体上,包括七个从锥虫[泛素水解酶(UH)获得的),预测的丝氨酸/苏氨酸蛋白激酶(STK),己糖转运蛋白,假定蛋白,三个匿名序列)和克鲁斯锥虫中的三个[泛素结合酶E2(UBE2),核糖体RNA甲基转移酶(rRNAmtr),蛋白酶体非ATPase调控亚基6(PSMD6)]。尽管种内差异,对染色体核型的分析允许将T.rangeli菌株分为与KP1(+)和KP1(-)基因型一致的两组。 Southern杂交显示,除己糖转运蛋白探针外,所有其他探针均产生能够区分KP1(+)和KP1(-)基因型的独特模式。 UH,STK和An-1A04探针仅与KP1(+)菌株的染色体杂交,可用作该组的标记。此外,迄今为止已测序的所有锥虫物种的保守区域中均存在的UBE2,rRNAmtr和PSMD6标记共同杂交至相同的T.rangeli染色体带,表明在这些物种中存在基因同调。在T.rangeli的KP1(+)和KP1(-)菌株中发现独特的分子核型是值得注意的,并且可以用作研究该寄生虫遗传变异性的新方法。这些发现与Southern杂交杂交结果一起证明,在kDNA水平上的差异可能与核DNA的变异有关。

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