Document Detail


Phosphorylation at threonine-18 in addition to phosphorylation at serine-19 on myosin-II regulatory light chain is a mitosis-specific event.
MedLine Citation:
PMID:  11891719     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Cell division is an inevitable and vitally indispensable event in cell life, when the nucleus and cytoskeleton undergo profound reorganization. Cytoplasmic division (cytokinesis) is known to occur immediately after the end of nuclear division, when the nuclear envelope breaks down, and chromosomes condense and segregate, but its driving mechanism remains enigmatic. Myosin, particularly myosin-II, is thought to be required for cytokinesis as a force-generating element, the activity of which is mainly regulated through phosphorylations on its 20-kDa regulatory light chains (RLCs). MATERIALS AND METHODS: Multiparameter flow cytometric analysis was performed on fixed HeLa S3 cells (suspension culture cells) sequentially stained with the polyclonal antibody (termed PP1) against both phosphorylated sites (serine-19 and threonine-18) on the RLC, and with propidium iodide for DNA. "Positive" cells were sorted, followed by their microscopic examination. Fluorescence microscopy was employed to visualize the cell-cycle-dependent distribution of immunolabeled diphosphorylated RLCs in both HeLa S3 and adherent HeLa cells. RESULTS AND CONCLUSIONS: Doubly phosphorylated myosin RLCs were highly expressed in mitotic cells, suggesting the positive regulatory role of diphosphorylation in the redistribution of RLCs between daughter cells and then in cytokinesis. The increased immunofluorescence signal from the phosphorylated forms of RLC, together with flow cytometry, provides a clue with which to investigate the mechanisms governing the function of nonmuscle myosins during various cell motile events, including cytokinesis.
Authors:
Bogdan I Gerashchenko; Kozue Ueda; Mizuki Hino; Hiroshi Hosoya
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Cytometry     Volume:  47     ISSN:  0196-4763     ISO Abbreviation:  Cytometry     Publication Date:  2002 Mar 
Date Detail:
Created Date:  2002-03-13     Completed Date:  2002-12-13     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8102328     Medline TA:  Cytometry     Country:  United States    
Other Details:
Languages:  eng     Pagination:  150-7     Citation Subset:  IM    
Copyright Information:
Copyright 2002 Wiley-Liss, Inc.
Affiliation:
Department of Biological Science, Graduate School of Science, Hiroshima University, 1-3-31 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8526, Japan.
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MeSH Terms
Descriptor/Qualifier:
Amino Acid Sequence / physiology
Antibody Specificity / immunology
Cell Cycle / physiology
Cell Division / physiology
Cytoskeleton
DNA / analysis
Fluorescent Antibody Technique
Hela Cells
Humans
Mitosis / physiology*
Myosin Light Chains / metabolism*
Myosin Type II / metabolism*
Phosphorylation
Serine / metabolism
Threonine / metabolism
Chemical
Reg. No./Substance:
0/Myosin Light Chains; 56-45-1/Serine; 72-19-5/Threonine; 9007-49-2/DNA; EC 3.6.1.-/Myosin Type II

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