Chenik Mehdi, Douagi Feriel, Ben Achour Yosser, Khalef Noureddine Ben, Ouakad Meriem, Louzir Hechmi, Dellagi Koussay
Laboratoire d'Immunopathologie, Vaccinologie et Génétique Moléculaire, Institut Pasteur de Tunis, 13, Place Pasteur, 1002, Tunis-Belvédère, Tunisia.
Parasitol Res. 2005 Dec;98(1):5-13. doi: 10.1007/s00436-005-0012-z. Epub 2005 Oct 20.
Here, we report the existence of two different mucolipin-like genes in Leishmania parasites. The Leishmania major mucolipin-like A and B genes (lmmlA and lmmlB) encode two proteins of 776 and 590 amino acids, respectively, and may be classified among the mucolipins family [transient receptors potential mucolipin (TRPML)] because (1) they include a large region that exhibits significant similarities with specific domains of ion transport proteins and transient receptors potential (TRP) channels, (2) they contain at least 173 residues that display significant homologies with conserved regions of different mucolipins from several species, and (3) as TRPMLs, they include six predicted transmembrane domains. Gene expression analysis reveals that lmmlB is upregulated in metacyclics and amastigotes relative to procyclics, while lmmlA is constitutively expressed in the three Leishmania developmental stages. These genes could constitute potential drug targets.
在此,我们报告利什曼原虫寄生虫中存在两种不同的类黏脂蛋白基因。硕大利什曼原虫类黏脂蛋白A和B基因(lmmlA和lmmlB)分别编码776和590个氨基酸的两种蛋白质,并且可能被归类于黏脂蛋白家族[瞬时受体电位黏脂蛋白(TRPML)],因为(1)它们包含一个与离子转运蛋白和瞬时受体电位(TRP)通道的特定结构域具有显著相似性的大区域,(2)它们包含至少173个与来自多个物种的不同黏脂蛋白的保守区域具有显著同源性的残基,以及(3)作为TRPML,它们包含六个预测的跨膜结构域。基因表达分析表明,相对于前鞭毛体,lmmlB在感染期和无鞭毛体中上调,而lmmlA在利什曼原虫的三个发育阶段中均持续表达。这些基因可能构成潜在的药物靶点。