Baticados Waren N, Witola William H, Inoue Noboru, Kim Jung-Yeon, Kuboki Noritaka, Xuan Xuenan, Yokoyama Naoaki, Sugimoto Chihiro
National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan.
J Vet Med Sci. 2005 Feb;67(2):157-64. doi: 10.1292/jvms.67.157.
During the attempt to seek T. congolense species-specific diagnostic antigens, we discovered one cDNA clone (P74) encoding 74 kDa putative abc1 protein (p74) from T. congolense PCF cDNA library. It has been suggested that members of the abc1 family are novel chaperonins and essential for both the mitochondrial electron transfer in the bc 1 complex and the coenzyme Q biosynthesis. Although abc1 protein in yeast has a nuclear or mitochondrial subcellular location, neither nuclear localization signal nor mitochondrial targeting signal was found within p74. Northern blot analysis revealed that the transcription level of P74 mRNA in bloodstream form (BSF) cells were 4 times higher than that in procyclic form cells. Western blot analysis also indicated that p74 was only expressed in T. congolense BSF cells, and revealed that molecular mass of native p74 was not 74 kDa but 56 kDa. This indicates extensive post-translational modification in p74. Although further characterization of p74 will be required, our findings provide implications for CoQ biosynthesis pathway in T. congolense.
在试图寻找刚果锥虫物种特异性诊断抗原的过程中,我们从刚果锥虫前循环期(PCF)cDNA文库中发现了一个编码74 kDa假定abc1蛋白(p74)的cDNA克隆(P74)。有人提出,abc1家族成员是新型伴侣蛋白,对bc1复合物中的线粒体电子传递和辅酶Q生物合成均至关重要。尽管酵母中的abc1蛋白定位于细胞核或线粒体,但在p74中未发现核定位信号或线粒体靶向信号。Northern印迹分析显示,血流形式(BSF)细胞中P74 mRNA的转录水平比前循环期细胞高4倍。Western印迹分析还表明,p74仅在刚果锥虫BSF细胞中表达,并显示天然p74的分子量不是74 kDa而是56 kDa。这表明p74存在广泛的翻译后修饰。尽管需要对p74进行进一步表征,但我们的发现为刚果锥虫中的辅酶Q生物合成途径提供了启示。