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Role of inhibitory factor IF1 during the differentiation of T. brucei
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SYSNO ASEP 0488334 Document Type O - Others R&D Document Type Others Title Role of inhibitory factor IF1 during the differentiation of T. brucei Author(s) Doleželová, Eva (BC-A) RID
Panicucci, Brian (BC-A)
Zíková, Alena (BC-A) RID, ORCIDYear of issue 2016 Language eng - English Country CZ - Czech Republic Keywords inhibitor factor ; IF1 ; T. brucei Subject RIV EB - Genetics ; Molecular Biology OECD category Biochemistry and molecular biology R&D Projects LL1205 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Institutional support BC-A - RVO:60077344 Annotation Trypanosoma brucei undergoes a complex life cycle as it alternates between a mammalian host and the blood-feeding insect vector, a tsetse fly. Due to the different environments, the distinct life stages differ in their energy metabolism, i.e. insect stage (procyclic cells, PF) depends on mitochondrial oxidative phosphorylation (OXPHOS) for ATP production while the bloodstream stage (BF) gains energy by aerobic glycolysis. The dramatic switch from the OXPHOS to glycolysis happens during the complex development of the PF in the tsetse fly. The molecular mechanism behind this shift is still unknown. Importantly, an induced over-expression of a differentiation factor, RNA-binding protein 6 (RBP6), results in the appearance of epimastigotes and metacyclic trypanosome in vitro (Kolev, 2012). We have established this RBP6 overexpressing cell line and the presence of the distinct cell types was verified using DAPI staining to visualize position of the kinetoplast to nuclei and by an endocytosis test. Moreover, we checked for changes in expression of subunits of respiratory complexes III and V. Interestingly, the level of T. brucei inhibitory factor 1 (TbIF1), a specific natural inhibitor of complex V, was significantly increased in the RBP6-induced cells. At the same time, we detected elevated levels of radical oxygen species (ROS) and changes in mitochondrial membrane potential. This is similar to what is reported in cancer cells, where high levels of IF1 expression inhibits ATP synthesis and creates a ROS signal that triggers the metabolic switch from OXPHOS to aerobic glycolysis. Determining how TbIF1 is regulated and what is the signaling mechanism during the trypanosome differentiation are important aims of this project. Workplace Biology Centre (since 2006) Contact Dana Hypšová, eje@eje.cz, Tel.: 387 775 214 Year of Publishing 2018 Electronic address http://www.parazitologie.cz/protozoologie/Protodny2016/JPD_sbornik_2016.pdf
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