Document Detail


Regulation of the cell division cycle in Trypanosoma brucei.
MedLine Citation:
PMID:  22865501     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The cell division cycle is tightly regulated by the activation and inactivation of a series of proteins that control the replication and segregation of organelles to the daughter cells. During the past decade, we have witnessed significant advances in our understanding of the cell cycle in Trypanosoma brucei and how the cycle is regulated by various regulatory proteins. However, many other regulators, especially those unique to trypanosomes, remain to be identified, and we are just beginning to delineate the signaling pathways that drive the transitions through different cell cycle stages, such as the G(1)/S transition, G(2)/M transition, and mitosis-cytokinesis transition. Trypanosomes appear to employ both evolutionarily conserved and trypanosome-specific molecules to regulate the various stages of its cell cycle, including DNA replication initiation, spindle assembly, chromosome segregation, and cytokinesis initiation and completion. Strikingly, trypanosomes lack some crucial regulators that are well conserved across evolution, such as Cdc6 and Cdt1, which are involved in DNA replication licensing, the spindle motor kinesin-5, which is required for spindle assembly, the central spindlin complex, which has been implicated in cytokinesis initiation, and the actomyosin contractile ring, which is located at the cleavage furrow. Conversely, trypanosomes possess certain regulators, such as cyclins, cyclin-dependent kinases, and mitotic centromere-associated kinesins, that are greatly expanded and likely play diverse cellular functions. Overall, trypanosomes apparently have integrated unique regulators into the evolutionarily conserved pathways to compensate for the absence of those conserved molecules and, additionally, have evolved certain cell cycle regulatory pathways that are either different from its human host or distinct between its own life cycle forms.
Authors:
Ziyin Li
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review     Date:  2012-08-03
Journal Detail:
Title:  Eukaryotic cell     Volume:  11     ISSN:  1535-9786     ISO Abbreviation:  Eukaryotic Cell     Publication Date:  2012 Oct 
Date Detail:
Created Date:  2012-10-02     Completed Date:  2013-02-21     Revised Date:  2013-07-12    
Medline Journal Info:
Nlm Unique ID:  101130731     Medline TA:  Eukaryot Cell     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1180-90     Citation Subset:  IM    
Affiliation:
Department of Microbiology & Molecular Genetics, University of Texas Medical School at Houston, TX, USA. Ziyin.Li@uth.tmc.edu
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Cell Cycle* / genetics
Cell Cycle Proteins / genetics,  metabolism
DNA Replication
DNA, Protozoan / biosynthesis
Protozoan Proteins / genetics,  metabolism
Trypanosoma brucei brucei / cytology,  genetics,  metabolism*
Grant Support
ID/Acronym/Agency:
AI090070/AI/NIAID NIH HHS; AI093897/AI/NIAID NIH HHS; R21 AI093897/AI/NIAID NIH HHS; R56 AI090070/AI/NIAID NIH HHS
Chemical
Reg. No./Substance:
0/Cell Cycle Proteins; 0/DNA, Protozoan; 0/Protozoan Proteins
Comments/Corrections

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


Previous Document:  cis- and trans-acting localization determinants of pH response regulator Rim13 in Saccharomyces cere...
Next Document:  New Multifunctional Porous Materials Based on Inorganic-Organic Hybrid Single-Walled Carbon Nanotube...