Use este identificador para citar ou linkar para este item: http://sgc.anlis.gob.ar/handle/123456789/1439
Título: The ubiquitin-conjugating enzyme CDC34 is essential for cytokinesis in contrast to putative subunits of a SCF complex in Trypanosoma brucei
Autor(es): Rojas, Federico 
Koszela, Joanna 
Bua, Jacqueline 
Llorente, Briardo 
Burchmore, Richard 
Auer, Manfred 
Mottram, Jeremy C. 
Téllez-Iñón, María Teresa 
Palavras-chave: Trypanosoma brucei brucei
Data do documento: 13-Jun-2017
Editora: Yes
Jornal: PLoS neglected tropical diseases 
Resumo: 
The ubiquitin-proteasome system is a post-translational regulatory pathway for controlling protein stability and activity that underlies many fundamental cellular processes, including cell cycle progression. Target proteins are tagged with ubiquitin molecules through the action of an enzymatic cascade composed of E1 ubiquitin activating enzymes, E2 ubiquitin conjugating enzymes, and E3 ubiquitin ligases. One of the E3 ligases known to be responsible for the ubiquitination of cell cycle regulators in eukaryotes is the SKP1-CUL1-F-box complex (SCFC). In this work, we identified and studied the function of homologue proteins of the SCFC in the life cycle of Trypanosoma brucei, the causal agent of the African sleeping sickness. Depletion of trypanosomal SCFC components TbRBX1, TbSKP1, and TbCDC34 by RNAi resulted in decreased growth rate and contrasting cell cycle abnormalities for both procyclic (PCF) and bloodstream (BSF) forms. Depletion of TbRBX1 in PCF cells interfered with kinetoplast replication, whilst depletion of TbSKP1 arrested PCF and BSF cells in the G1/S transition. Silencing of TbCDC34 in BSF cells resulted in a block in cytokinesis and caused rapid clearance of parasites from infected mice. We also show that TbCDC34 is able to conjugate ubiquitin in vitro and in vivo, and that its activity is necessary for T. brucei infection progression in mice. This study reveals that different components of a putative SCFC have contrasting phenotypes once depleted from the cells, and that TbCDC34 is essential for trypanosome replication, making it a potential target for therapeutic intervention.
Descrição: 
Fil: Rojas, Federico. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular (INGEBI-CONICET), Buenos Aires, Argentina.

Fil: Koszela, Joanna. Institute of Quantitative Biology Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, King's Buildings, Edinburgh; Reino Unido.

Fil: Bua, Jacqueline. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología; Argentina.

Fil: Llorente, Briardo. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular (INGEBI-CONICET), Buenos Aires, Argentina.

Fil: Burchmore, Richard. Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom

Fil: Auer, Manfred. . Institute of Quantitative Biology Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, King's Buildings, Edinburgh; Reino Unido.

Fil: Mottram, Jeremy C. Centre for Immunology and Infection, Department of Biology, University of York, York; Reino Unido.

Fil: Téllez-Iñón, María Teresa. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular (INGEBI-CONICET), Buenos Aires, Argentina.
URI: http://sgc.anlis.gob.ar/handle/123456789/1439
ISSN: 1935-2735
DOI: 10.1371/journal.pntd.0005626
Direitos: Open Access
Aparece nas Coleções:Publicaciones INP

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