Important role of Ser 219 phosphorylation of TRF1 in regulation of cell cycle.
- Author:
Yi-yi XU
1
;
Jian-ping LAN
;
Yuan-yuan ZHU
Author Information
- Publication Type:Journal Article
- MeSH: Ataxia Telangiectasia Mutated Proteins; Cell Cycle; genetics; physiology; Cell Cycle Proteins; metabolism; DNA-Binding Proteins; metabolism; Green Fluorescent Proteins; genetics; metabolism; HeLa Cells; Humans; Immunoblotting; Microscopy, Fluorescence; Mutation; Phosphorylation; Protein-Serine-Threonine Kinases; metabolism; Recombinant Fusion Proteins; genetics; metabolism; Serine; genetics; metabolism; Telomeric Repeat Binding Protein 1; genetics; metabolism; physiology; Transfection; Tumor Suppressor Proteins; metabolism
- From: Journal of Zhejiang University. Medical sciences 2007;36(4):325-330
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the role of Ser 219 phosphorylation of TRF1 (telomere repeat binding factor 1) in regulation of cell cycle.
METHODSThe mimicking phosphorylation mutant (TRF1S219D-GFP) and the non-phosphorylatable mutant (TRF1S219A-GFP) were constructed; the mutant genes and corresponding proteins were checked by sequencing and Western blot, respectively. Immunofluorescence staining was performed to detect the localization of mutants in HeLa cells. Cell cycle was analyzed by flow cytometry and ATM level was evaluated by immunoblotting.
RESULTSThe mutant genes were verified by direct sequencing and protein expression of GFP-tagged mutants was confirmed by immunoblotting.TRF1S219A-GFP and TRF1S219D-GFP were both localized in telomere of HeLa cells. Moreover, overexpression of TRF1-GFP or TRF1S219A-GFP resulted in an accumulation of HeLa cells in G2/M (P<0.05). The protein level of ATM was increased when overexpression the wide type or mutants.
CONCLUSIONThe Ser 219 phosphorylation of TRF1 by ATM could result in cell cycle arrest in G2/M, which is related to overexpression of TRF1.
