Department of Biological Sciences, Birla Institute of Technology and Science, Pilani, Rajasthan, India.
Acta Trop. 2012 Apr;122(1):138-49. doi: 10.1016/j.actatropica.2012.01.007. Epub 2012 Jan 10.
The apicomplexan parasite Plasmodium vivax is responsible for causing more than 70% of human malaria cases in Central and South America, Southeastern Asia and the Indian subcontinent. The rising severity of the disease and the increasing incidences of resistance shown by this parasite towards usual therapeutic regimens have necessitated investigation of putative novel drug targets to combat this disease. The apicoplast, an organelle of procaryotic origin, and its circular genome carrying genes of possible functional importance, are being looked upon as potential drug targets. The genes on this circular genome are believed to be highly conserved among all Plasmodium species. Till date, the plastid genome of P. falciparum, P. berghei and P. chabaudi have been detailed while partial sequences of some genes from other parasites including P. vivax have been studied for identifying evolutionary positions of these parasites. The functional aspects and significance of most of these genes are still hypothetical. In one of our previous reports, we have detailed the complete sequence, as well as structural and functional characteristics of the Elongation factor encoding tufA gene from the plastid genome of P. vivax. We present here the sequences of large and small subunit rRNA (lsu and ssu rRNA) genes, sufB (ORF470) gene, RNA polymerase (rpo B, C) subunit genes and clpC (casienolytic protease) gene from the plastid genome of P. vivax. A comparative analysis of these genes between P. vivax and P. falciparum reveals approximately 5-16% differences. A codon usage analysis of major plastid genes has shown a high frequency of codons rich in A/T at any or all of the three positions in all the species. TTA, AAT, AAA, TAT, and ATA are the major preferred codons. The sequences, functional domains and structural analysis of respective proteins do not show any variations in the active sites. A comparative analysis of these Indian P. vivax plastid genome encoded genes has also been done to understand the evolutionary position of the Indian parasite in comparison to other Plasmodium species.
间日疟原虫是引起中美洲、南美洲、东南亚和印度次大陆超过 70%人类疟疾病例的罪魁祸首。这种寄生虫对常规治疗方案的耐药性日益严重,因此需要寻找潜在的新药物靶点来对抗这种疾病。质体,一种原核起源的细胞器,及其携带可能具有重要功能的基因的环状基因组,正被视为潜在的药物靶点。据信,这个环状基因组上的基因在所有疟原虫物种中高度保守。迄今为止,已详细研究了恶性疟原虫、伯氏疟原虫和约氏疟原虫的质体基因组,而其他寄生虫(包括间日疟原虫)的一些基因的部分序列也已被研究,以确定这些寄生虫的进化地位。这些基因的大多数功能方面和意义仍然是假设的。在我们之前的一份报告中,我们详细介绍了来自间日疟原虫质体基因组的延伸因子编码 tufA 基因的完整序列、结构和功能特征。在这里,我们展示了来自间日疟原虫质体基因组的大亚基和小亚基 rRNA(lsu 和 ssu rRNA)基因、sufB(ORF470)基因、RNA 聚合酶(rpoB、C)亚基基因和 clpC(解旋酶蛋白酶)基因的序列。在间日疟原虫和恶性疟原虫之间对这些基因进行比较分析表明,它们之间存在大约 5-16%的差异。对主要质体基因的密码子使用分析表明,在所有物种的三个位置中的任意一个或全部位置上,A/T 丰富的密码子出现的频率都很高。TTA、AAT、AAA、TAT 和 ATA 是主要的偏好密码子。在活性位点没有发现任何变异。还对这些印度间日疟原虫质体基因组编码基因进行了比较分析,以了解与其他疟原虫物种相比,印度寄生虫的进化地位。