Document Detail


The small ubiquitin-like modifier (SUMO) is essential in cell cycle regulation in Trypanosoma brucei.
MedLine Citation:
PMID:  20045687     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
SUMO, a reversible post-translational protein modifier, plays important roles in many processes of higher eukaryotic cell life. Although SUMO has been identified in many eukaryotes, SUMO and SUMO system are still unknown in some eukaryotic unicellular organisms, such as Trypanosoma brucei (T. brucei). In this study, only one SUMO homologue (TbSUMO) was identified in T. brucei. Expression of TbSUMO was knocked down by using RNA interference technique in procyclic-form T. brucei. The growth of TbSUMO-deficient cells was significantly inhibited. TbSUMO-deficient cells were arrested in G2/M phase accompanied with an obvious increase of 0N1K cells (zoids), and failed in chromosome segregation. These results indicate that TbSUMO is essential in cell cycle regulation, with one important role in mitosis. Meanwhile, the enrichment of zoids suggests the inhibition of mitosis does not prevent the cell division in procyclic-form T. brucei. HA-tagged TbSUMO was overexpressed in T. brucei and was shown to be localized to the nucleus through the whole cell cycle, further revealing its distinguished functions in nucleus. All these accumulated data imply that a SUMO system essential for regulating cell cycle progression might exist in the procyclic-form T. brucei.
Authors:
Shanhui Liao; Tao Wang; Kai Fan; Xiaoming Tu
Related Documents :
15611627 - Cell cycle dependent regulation of the origin recognition complex.
14533007 - Rb1cc1 suppresses cell cycle progression through rb1 expression in human neoplastic cells.
11545167 - Tik+ tok+: an embryonic clock?
14556967 - Induction of cell cycle regulatory proteins by murine b cell proliferating pectic polys...
3872327 - Analysis of the binding and postbinding activities of an inducible cloned ctl line at t...
5274477 - Introduction of a heterologous nucleus into enucleated cytoplasms of cultured mouse l-c...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-01-04
Journal Detail:
Title:  Experimental cell research     Volume:  316     ISSN:  1090-2422     ISO Abbreviation:  Exp. Cell Res.     Publication Date:  2010 Mar 
Date Detail:
Created Date:  2010-02-22     Completed Date:  2010-03-25     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0373226     Medline TA:  Exp Cell Res     Country:  United States    
Other Details:
Languages:  eng     Pagination:  704-15     Citation Subset:  IM    
Copyright Information:
2009 Elsevier Inc. All rights reserved.
Affiliation:
Hefei National Laboratory for Physical Sciences at Microscale, School of Life Science, University of Science and Technology of China, Hefei, Anhui 230026, PR China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Amino Acid Sequence
Animals
Antimetabolites / metabolism
Bromodeoxyuridine / metabolism
Cell Cycle / physiology*
Cell Nucleus / metabolism
Humans
Mitotic Spindle Apparatus / metabolism,  ultrastructure
Molecular Sequence Data
Protein Processing, Post-Translational*
Protozoan Proteins / genetics,  metabolism*
RNA Interference
SUMO-1 Protein / genetics,  metabolism*
Sequence Alignment
Sequence Homology, Amino Acid
Trypanosoma brucei brucei / cytology,  physiology*
Chemical
Reg. No./Substance:
0/Antimetabolites; 0/Protozoan Proteins; 0/SUMO-1 Protein; 59-14-3/Bromodeoxyuridine

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


Previous Document:  Mago Nashi, Tsunagi/Y14, and Ranshi form a complex that influences oocyte differentiation in Drosoph...
Next Document:  Paragonimus westermani: Identification and characterization of the fasciclin I domain-containing pro...