Kim Dong, Chiurillo Miguel Angel, El-Sayed Najib, Jones Kristin, Santos Márcia R M, Porcile Patricio E, Andersson Bjorn, Myler Peter, da Silveira José Franco, Ramírez José Luis
Departamento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, UNIFESP, Rua Botucatu, 862, CEP 04023-062, S. Paulo, Brazil.
Gene. 2005 Feb 14;346:153-61. doi: 10.1016/j.gene.2004.10.014. Epub 2005 Jan 28.
Here, we sequenced two large telomeric regions obtained from the pathogen protozoan Trypanosoma cruzi. These sequences, together with in silico assembled contigs, allowed us to establish the general features of telomeres and subtelomeres of this parasite. Our findings can be summarized as follows: We confirmed the presence of two types of telomeric ends; subtelomeric regions appeared to be enriched in (pseudo)genes of RHS (retrotransposon hot spot), TS (trans-sialidase)-like proteins, and putative surface protein DGF-1 (dispersed gene family-1). Sequence analysis of the ts-like genes located at the telomeres suggested that T. cruzi chromosomal ends could have been the site for generation of new gp85 variants, an important adhesin molecule involved in the invasion of mammalian cells by T. cruzi. Finally, a mechanism for generation of T. cruzi telomere by chromosome breakage and telomere healing is proposed.
在此,我们对从病原体原生动物克氏锥虫获得的两个大型端粒区域进行了测序。这些序列,连同通过计算机组装的重叠群,使我们能够确定该寄生虫端粒和亚端粒的一般特征。我们的研究结果可总结如下:我们证实了存在两种类型的端粒末端;亚端粒区域似乎富含RHS(逆转座子热点)、TS(转唾液酸酶)样蛋白和假定的表面蛋白DGF-1(分散基因家族-1)的(假)基因。对位于端粒的ts样基因的序列分析表明,克氏锥虫染色体末端可能是新的gp85变体产生的位点,gp85是一种重要的粘附分子,参与克氏锥虫对哺乳动物细胞的侵袭。最后,提出了一种通过染色体断裂和端粒修复产生克氏锥虫端粒的机制。