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SUMO-1 modification of centrosomal protein hNinein promotes hNinein nuclear localization.
- Source :
-
Life sciences [Life Sci] 2006 Feb 02; Vol. 78 (10), pp. 1114-20. Date of Electronic Publication: 2005 Sep 09. - Publication Year :
- 2006
-
Abstract
- A centrosomal-associated protein, ninein is a microtubules minus end capping, centrosome position, and anchoring protein, but the underlying structure and physiological functions are still unknown. To identify the molecules that regulate the function of human ninein in centrosome, we performed yeast two-hybrid screen and isolated the SUMO-conjugating E2 enzyme, Ubc9, and SUMOylation enhancing enzymes, including PIAS1 and PIASxalpha, as binding partners of hNinein. These interactions as well as the interaction between hNinein and SUMO-1 are also confirmed by a glutathione S-transferase (GST) pull-down experiment. Furthermore, the C-terminal region of hNinein can be SUMOylated in vitro and in HeLa cells transfected with a plasmid expressing GFP-hNinein. Our findings firstly place SUMOylation target on the centrosome structure protein, hNinein, which results in the switch localization from centrosome to nucleus, suggesting the importance of the SUMOylation of hNinein and probably other centrosomal proteins may also be involved in the centrosome activity.
- Subjects :
- Cells, Cultured
Cytoskeletal Proteins
DNA, Complementary biosynthesis
DNA, Complementary genetics
Escherichia coli genetics
Escherichia coli metabolism
GTP-Binding Proteins genetics
Glutathione metabolism
Humans
Immunoblotting
Immunoprecipitation
In Situ Hybridization
Microscopy, Fluorescence
Mutagenesis, Site-Directed
Nuclear Proteins
Plasmids genetics
Protein Transport genetics
Protein Transport physiology
Saccharomyces cerevisiae metabolism
Transfection
Cell Nucleus metabolism
Centrosome metabolism
GTP-Binding Proteins metabolism
SUMO-1 Protein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0024-3205
- Volume :
- 78
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Life sciences
- Publication Type :
- Academic Journal
- Accession number :
- 16154161
- Full Text :
- https://doi.org/10.1016/j.lfs.2005.06.021