Characterization of two different mucolipin-like genes from Leishmania major
- 21 October 2005
- journal article
- Published by Springer Nature in Zeitschrift Fur Parasitenkunde-Parasitology Research
- Vol. 98 (1) , 5-13
- https://doi.org/10.1007/s00436-005-0012-z
Abstract
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.Keywords
This publication has 49 references indexed in Scilit:
- Transient receptor potential and other ion channels as pharmaceutical targets in airway smooth muscle cellsRespirology, 2004
- Functional links between mucolipin-1 and Ca2+-dependent membrane trafficking in mucolipidosis IVBiochemical and Biophysical Research Communications, 2004
- TRP Channels as Drug TargetsPublished by Wiley ,2004
- TRP channels as cellular sensorsNature, 2003
- International Union of Pharmacology. XLIII. Compendium of Voltage-Gated Ion Channels: Transient Receptor Potential ChannelsPharmacological Reviews, 2003
- Identification of a Disulfide Isomerase Protein ofLeishmania majoras a Putative Virulence FactorInfection and Immunity, 2002
- Mucolipidosis Type IVMolecular Genetics and Metabolism, 2001
- Subversion of a young phagosome: the survival strategies of intracellular pathogens. MicroreviewCellular Microbiology, 2000
- Real time quantitative PCR.Genome Research, 1996
- LeishmaniasisClinics in Dermatology, 1996