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Assembling Fe/S-clusters and modifying tRNAs: ancient co-factors meet ancient adaptors
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SYSNO ASEP 0364802 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Assembling Fe/S-clusters and modifying tRNAs: ancient co-factors meet ancient adaptors Author(s) Alfonzo, J. D. (US)
Lukeš, Julius (BC-A) RID, ORCIDSource Title Trends in Parasitology. - : Elsevier - ISSN 1471-4922
Roč. 27, č. 6 (2011), 234-237Number of pages 4 s. Language eng - English Country GB - United Kingdom Keywords IRON-SULFUR CLUSTERS ; TRYPANOSOMA-BRUCEI ; MITOCHONDRIAL ; PROTEIN ; FRATAXIN ; BIOSYNTHESIS ; SYNTHETASES ; BIOGENESIS ; THIOLATION ; ANTICODON Subject RIV EB - Genetics ; Molecular Biology R&D Projects LC07032 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) 2B06129 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GA204/09/1667 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z60220518 - PAU-O, BC-A (2005-2011) UT WOS 000292238800003 DOI 10.1016/j.pt.2011.02.003 Annotation Trypanosome brucei undergoes two clearly distinct develomental stages: in the insect vector (procyclic stage) the cells generate the bulk of their energy through respiration, whereas in the bloodstream of the mammalian host (bloodstream stage) they grow mostly glycolytically. Several mitochondrial respiratory proteins require iron-sulfur clusters for activity, and their activation coincides with developmental changes. Likewise some tRNA modification enzymes either require iron-sulfur clusters or use components of the iron-sulfur cluster assembly pathway for activity. These enzymes affect the anticodon loop of various tRNAs and can impact protein synthesis. Herein, the possibility of these pathways being integrated and exploited by T. brucei to carefully coordinate energy demands to translational rates in response to enviromental changes is examined. Workplace Biology Centre (since 2006) Contact Dana Hypšová, eje@eje.cz, Tel.: 387 775 214 Year of Publishing 2012
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