Document Detail


Phosphorylation of the mitotic regulator protein Hec1 by Nek2 kinase is essential for faithful chromosome segregation.
MedLine Citation:
PMID:  12386167     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hec1 (highly expressed in cancer) plays essential roles in chromosome segregation by interacting through its coiled-coil domains with several proteins that modulate the G(2)/M phase. Hec1 localizes to kinetochores, and its inactivation either by genetic deletion or antibody neutralization leads to severe and lethal chromosomal segregation errors, indicating that Hec1 plays a critical role in chromosome segregation. The mechanisms by which Hec1 is regulated, however, are not known. Here we show that human Hec1 is a serine phosphoprotein and that it binds specifically to the mitotic regulatory kinase Nek2 during G(2)/M. Nek2 phosphorylates Hec1 on serine residue 165, both in vitro and in vivo. Yeast cells are viable without scNek2/Kin3, a close structural homolog of Nek2 that binds to both human and yeast Hec1. When the same yeasts carry an scNek2/Kin3 (D55G) or Nek2 (E38G) mutation to mimic a similar temperature-sensitive nima mutation in Aspergillus, their growth is arrested at the nonpermissive temperature, because the scNek2/Kin3 (D55G) mutant binds to Hec1 but fails to phosphorylate it. Whereas wild-type human Hec1 rescues lethality resulting from deletion of Hec1 in Saccharomyces cerevesiae, a human Hec1 mutant or yeast Hec1 mutant changing Ser(165) to Ala or yeast Hec1 mutant changing Ser(201) to Ala does not. Mutations changing the same Ser residues to Glu, to mimic the negative charge created by phosphorylation, partially rescue lethality but result in a high incidence of errors in chromosomal segregation. These results suggest that cell cycle-regulated serine phosphorylation of Hec1 by Nek2 is essential for faithful chromosome segregation.
Authors:
Yumay Chen; Daniel J Riley; Lei Zheng; Phang-Lang Chen; Wen-Hwa Lee
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.     Date:  2002-10-16
Journal Detail:
Title:  The Journal of biological chemistry     Volume:  277     ISSN:  0021-9258     ISO Abbreviation:  J. Biol. Chem.     Publication Date:  2002 Dec 
Date Detail:
Created Date:  2002-12-16     Completed Date:  2003-02-12     Revised Date:  2013-02-07    
Medline Journal Info:
Nlm Unique ID:  2985121R     Medline TA:  J Biol Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  49408-16     Citation Subset:  IM    
Affiliation:
Institute of Biotechnology, Department of Molecular Medicine, University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, TX 78245-3207, USA.
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MeSH Terms
Descriptor/Qualifier:
Alanine / chemistry
Amino Acid Sequence
Amino Acids / chemistry
Blotting, Western
Cell Cycle
Chromosome Segregation
DNA, Complementary / metabolism
Escherichia coli / metabolism
G2 Phase
Genotype
Glutathione Transferase / metabolism
Humans
Mitosis*
Molecular Sequence Data
Mutation
Nuclear Proteins / metabolism*
Phosphorylation
Precipitin Tests
Protein Binding
Protein-Serine-Threonine Kinases / metabolism*
Recombinant Fusion Proteins / metabolism
Saccharomyces cerevisiae / genetics
Saccharomyces cerevisiae Proteins / metabolism
Serine / chemistry,  metabolism
Temperature
Time Factors
Tumor Cells, Cultured
Grant Support
ID/Acronym/Agency:
CA 58318/CA/NCI NIH HHS; CA 81020/CA/NCI NIH HHS; EY 05758-18/EY/NEI NIH HHS; R01 CA107568/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Amino Acids; 0/DNA, Complementary; 0/NDC80 protein, human; 0/Nuclear Proteins; 0/Recombinant Fusion Proteins; 0/Saccharomyces cerevisiae Proteins; 56-41-7/Alanine; 56-45-1/Serine; EC 2.5.1.18/Glutathione Transferase; EC 2.7.1.-/NEK2 protein, human; EC 2.7.11.1/KIN3 protein, S cerevisiae; EC 2.7.11.1/Protein-Serine-Threonine Kinases

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