Document Detail


The CRK3 protein kinase is essential for cell cycle progression of Leishmania mexicana.
MedLine Citation:
PMID:  11295173     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Leishmania mexicana CRK3 gene encodes a cdc2-related protein kinase with activity towards histone H1. Attempts to disrupt both alleles of CRK3 in the promastigote life-cycle stage resulted in changes in cell ploidy, which were avoided only when an extra copy of CRK3 was expressed from an episome. This provides strong evidence that CRK3 is essential to L. mexicana. The cyclin-dependent kinase specific inhibitor flavopiridol inhibited affinity purified histidine tagged CRK3 (CRK3his) with an IC(50) value of 100 nM and inhibited in vitro growth of L. mexicana promastigotes. Incubation of promastigotes with 2.5 microM flavopiridol for 24 h led to cell cycle arrest with an accumulation of 95% of cells in G2 or early mitosis (G2/M). Release from cell cycle arrest resulted in a semi-synchronous re-entry into the cell cycle; samples taken at 2, 4, and 6 h after release from the block were enriched for cells in G1 (68%), S-phase (70%), and G2/M phase (61%), respectively. This method of synchronisation was used to show that the majority of CRK3his activity towards the substrate histone H1 was present at G2/M. These data suggest that CRK3 has an essential role in controlling cell cycle progression at the G2/M-phase transition in L. mexicana promastigotes.
Authors:
P Hassan; D Fergusson; K M Grant; J C Mottram
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Molecular and biochemical parasitology     Volume:  113     ISSN:  0166-6851     ISO Abbreviation:  Mol. Biochem. Parasitol.     Publication Date:  2001 Apr 
Date Detail:
Created Date:  2001-04-11     Completed Date:  2001-09-20     Revised Date:  2012-08-01    
Medline Journal Info:
Nlm Unique ID:  8006324     Medline TA:  Mol Biochem Parasitol     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  189-98     Citation Subset:  IM    
Affiliation:
Wellcome Centre for Molecular Parasitology, University of Glasgow, Anderson College, 56 Dumbarton Road, G11 6NU, Scotland, Glasgow, UK.
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MeSH Terms
Descriptor/Qualifier:
Animals
CDC2 Protein Kinase
Cell Cycle / drug effects,  physiology*
Cyclin-Dependent Kinases / antagonists & inhibitors,  genetics,  metabolism*
Enzyme Inhibitors / pharmacology
Flavonoids / pharmacology
Gene Expression Regulation
Leishmania mexicana / cytology*,  enzymology*,  genetics
Piperidines / pharmacology
Protozoan Proteins
Chemical
Reg. No./Substance:
0/Enzyme Inhibitors; 0/Flavonoids; 0/Piperidines; 0/Protozoan Proteins; 146426-40-6/flavopiridol; EC 2.7.11.22/CDC2 Protein Kinase; EC 2.7.11.22/Cyclin-Dependent Kinases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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