Yatawara Lalani, Le Thanh Hoa, Wickramasinghe Susiji, Agatsuma Takeshi
Department of Environmental Health Sciences, Kochi Medical School, Oko, Nankoku City, Kochi 783-8505, Japan.
Gene. 2008 Nov 15;424(1-2):80-6. doi: 10.1016/j.gene.2008.07.026. Epub 2008 Jul 30.
We report 8420 bp of DNA sequence data from the maxicircle (mitochondrial) genome of Leishmania major (MHOM/SU/73/5ASKH), a much larger portion of this genome than has been reported previously from any Leishmania species infecting humans. This region contains 10 partial and complete genes: 5 protein-encoding genes (COII, COIII, ND1, ND7 and Cyt b); two ribosomal RNA subunits (12S and 9S) and three unidentified open reading frames (MURF1, MURF4 (ATPase6) and MURF5), as in the lizard-infecting species L. tarentolae. The genes from L. major exhibit 85-87% identity with those of L. tarentolae at the nucleotide level and 71-94% identity at the amino acid level. Most differences between sequences from the two species are transversions. The gene order and arrangement within the maxicircle of L. major are similar to those in L. tarentolae, but base composition and codon usage differ between the species. Codons assigned for initiation for protein-coding genes available for comparison are similar in five genes in the two species. Pre-editing was identified in some of the protein-coding genes. Short intergenic non-coding regions are also present in L. major as they are in L. tarentolae. Intergenic regions between 9S rRNA and MURF5, MURF1 and ND1 genes are G+C rich and considered to be extensive RNA editing regions. The RNA editing process is likely to be conserved in similar pattern in L. major as in L. tarentolae.
我们报告了来自硕大利什曼原虫(MHOM/SU/73/5ASKH)大圆环(线粒体)基因组的8420个碱基对的DNA序列数据,这一基因组区域比之前报道的任何感染人类的利什曼原虫物种的该区域都要大得多。该区域包含10个部分和完整的基因:5个蛋白质编码基因(COII、COIII、ND1、ND7和Cyt b);两个核糖体RNA亚基(12S和9S)以及三个未鉴定的开放阅读框(MURF1、MURF4(ATPase6)和MURF5),与感染蜥蜴的塔兰托利什曼原虫中的情况相同。硕大利什曼原虫的基因在核苷酸水平上与塔兰托利什曼原虫的基因具有85 - 87%的同一性,在氨基酸水平上具有71 - 94%的同一性。两个物种序列之间的大多数差异是颠换。硕大利什曼原虫大圆环内的基因顺序和排列与塔兰托利什曼原虫的相似,但两个物种的碱基组成和密码子使用情况不同。在两个物种中可用于比较的蛋白质编码基因的起始密码子在五个基因中相似。在一些蛋白质编码基因中发现了预编辑现象。硕大利什曼原虫中也存在短的基因间非编码区域,就像塔兰托利什曼原虫中一样。9S rRNA与MURF5、MURF1与ND1基因之间的基因间区域富含G + C,被认为是广泛的RNA编辑区域。RNA编辑过程在硕大利什曼原虫中可能与在塔兰托利什曼原虫中以相似模式保守。