Mendonca S M, Campos C B, Gueiros-Filho F J, Lopes U G
Departamento de Patologia e Laboratorios, Faculdade de Ciencias Medicas, Universidade do Estado do Rio de Janeiro, Brazil.
Biol Res. 1993;26(1-2):3-9.
A PCR based assay was designed in order to amplify putative ras gene sequences of the GTPase superfamily eventually present in Leishmania amazonensis and Trypanosoma cruzi. A set of primers corresponding to the conserved motifs G1 and G3 of the GTP binding proteins was synthesized. Sequencing of six PCR products (three from Leishmania and three from Trypanosoma) identified, however, two other different GTPases. The 270 bp L. amazonensis clone, pLef-11, shared an amino acid identity of around 80% with an eukaryotic elongation factor 1a of protein synthesis. On the other hand, the 168 bp T. cruzi clone, pTCr1, demonstrated over 60% amino acid identity to ras-related proteins of the rab-YPT-SEC4 family involved in control of vesicular traffic. To our knowledge, this is the first report of GTP binding protein genes in trypanosomatids.
设计了一种基于聚合酶链反应(PCR)的检测方法,以扩增最终存在于亚马逊利什曼原虫和克氏锥虫中的GTP酶超家族假定的ras基因序列。合成了一组对应于GTP结合蛋白保守基序G1和G3的引物。然而,对六个PCR产物(三个来自利什曼原虫,三个来自锥虫)进行测序后,鉴定出另外两种不同的GTP酶。270 bp的亚马逊利什曼原虫克隆pLef-11与蛋白质合成的真核延伸因子1a的氨基酸同一性约为80%。另一方面,168 bp的克氏锥虫克隆pTCr1与参与囊泡运输控制的rab-YPT-SEC4家族的ras相关蛋白的氨基酸同一性超过60%。据我们所知,这是首次在锥虫中报道GTP结合蛋白基因。