Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8648353 | Molecular and Biochemical Parasitology | 2018 | 37 Pages |
Abstract
The procyclic form of the human parasite Trypanosoma brucei harbors one single, large mitochondrion containing all tricarboxylic acid (TCA) cycle enzymes and respiratory chain complexes present also in higher eukaryotes. Metabolite exchange among subcellular compartments such as the cytoplasm, the mitochondrion, and the peroxisomes is crucial for redox homeostasis and for metabolic pathways whose enzymes are dispersed among different organelles. In higher eukaryotes, mitochondrial carrier family (MCF) proteins transport TCA-cycle intermediates across the inner mitochondrial membrane. Previously, we identified several MCF members that are essential for T. brucei survival. Among these, only one MCF protein, TbMCP12, potentially could transport dicarboxylates and tricarboxylates. Here, we conducted phylogenetic and sequence analyses and functionally characterised TbMCP12 in vivo. Our results suggested that similarly to its homologues in plants, TbMCP12 transports both dicarboxylates and tricarboxylates across the mitochondrial inner membrane. Deleting this carrier in T. brucei was not lethal, while its overexpression was deleterious. Our results suggest that the intracellular abundance of TbMCP12 is an important regulatory element for the NADPH balance and mitochondrial ATP-production.
Keywords
DICOxoglutarate carrierCarboxyatractylosideBSDOGCDTCTrypanosoma bruceiCITNEOTCAMCFCATROSBlasticidindicarboxylate carrierMitochondrial transportMitochondrial carrier familyDicarboxylateEnergy metabolismUTR یا untranslated regions untranslated regionNeomycincitrate carriertricarboxylic acid cycleReactive oxygen species
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Molecular Biology
Authors
Claudia Colasante, Fuli Zheng, Cordula Kemp, Frank Voncken,