Document Detail


Cell cycle regulation in Trypanosoma brucei.
MedLine Citation:
PMID:  17335918     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cell division is regulated by intricate and interconnected signal transduction pathways that precisely coordinate, in time and space, the complex series of events involved in replicating and segregating the component parts of the cell. In Trypanosoma brucei, considerable progress has been made over recent years in identifying molecular regulators of the cell cycle and elucidating their functions, although many regulators undoubtedly remain to be identified, and there is still a long way to go with respect to determining signal transduction pathways. However, it is clear that cell cycle regulation in T. brucei is unusual in many respects. Analyses of trypanosome orthologues of conserved eukaryotic cell cycle regulators have demonstrated divergence of their function in the parasite, and a number of other key regulators are missing from T. brucei. Cell cycle regulation differs in different parasite life cycle stages, and T. brucei appears to use different checkpoint control strategies compared to model eukaryotes. It is therefore probable that T. brucei has evolved novel pathways to control its cell cycle.
Authors:
Tansy C Hammarton
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2007-02-04
Journal Detail:
Title:  Molecular and biochemical parasitology     Volume:  153     ISSN:  0166-6851     ISO Abbreviation:  Mol. Biochem. Parasitol.     Publication Date:  2007 May 
Date Detail:
Created Date:  2007-04-09     Completed Date:  2007-06-21     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  8006324     Medline TA:  Mol Biochem Parasitol     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  1-8     Citation Subset:  IM    
Affiliation:
Division of Infection & Immunity and Wellcome Centre for Molecular Parasitology, University of Glasgow, Biomedical Research Centre, 120 University Place, Glasgow G12 8TA, United Kingdom. t.hammarton@bio.gla.ac.uk
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MeSH Terms
Descriptor/Qualifier:
Animals
Cell Cycle / physiology*
Cell Division
Cyclin-Dependent Kinases / metabolism
Cytokinesis
G1 Phase
G2 Phase
Phosphoric Monoester Hydrolases / metabolism
RNA Interference
S Phase
Signal Transduction
Trypanosoma brucei brucei / cytology*,  genetics,  metabolism
Grant Support
ID/Acronym/Agency:
//Wellcome Trust
Chemical
Reg. No./Substance:
EC 2.7.11.22/Cyclin-Dependent Kinases; EC 3.1.3.-/Phosphoric Monoester Hydrolases
Comments/Corrections

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