ZHU Ying-bao,HAN Yun,SUN Yan,LIANG Li,JIA Ting-zhen.DNA repair protein degradation mediated by helicase-like transcription factor in radiation-induced apoptotic cells[J].Chinese Journal of Radiological Medicine and Protection,2010,30(5):510-512
DNA repair protein degradation mediated by helicase-like transcription factor in radiation-induced apoptotic cells
Received:April 13, 2010  
DOI:
KeyWords:Apoptosis  Helicase-like transcription factor (HLTF)  RING domain
FundProject:国家自然科学基金(30470976)
Author NameAffiliationE-mail
ZHU Ying-bao Medical Research Center, Peking University Third Hospital, Beijing 100083, China yingbaozhu@medmail.com.cn 
HAN Yun Medical Research Center, Peking University Third Hospital, Beijing 100083, China  
SUN Yan Medical Research Center, Peking University Third Hospital, Beijing 100083, China  
LIANG Li 肿瘤化疗与放射病科  
JIA Ting-zhen 肿瘤化疗与放射病科  
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Abstract::
      Objective To study the effects of helicase-like transcription factor (HLTF) transfection on DNA repair protein level in radiation-induced apoptotic cells. Methods Human lung carcinoma A549 cells were cultured and transfected with FLAG-tagged wild type HLTF (wild type HLTF transfection group), RING structure domain (ubiquitin conjugating region) mutatation HLTF expressing plasmid (mutant transfection group), empty plasmid (congtrol group) respectively. And the other cells were used as mock transfection group. All cells were irradiated with 15 Gy of 60Co γ-rays to induce apoptosis. Western blotting was used to detect the protein levels of the DNA repair proteins HRAD17 and HRAD52 in the transfected cells. Results The levels of HRAD17 and HRAD52 in the wild type HLTF transfection group was significantly lower than that of the control group. There was no significant difference in HRAD17 and HRAD52 levels between the mock transfection group and ubiquity in conjugating region mutation group. complexes of HLTF and HRAD17 and HRAD52 could be found in the irradiation-induced cells. Conclusions HLTF mediates the degradation of HRAD17 and HRAD52 in the irradiation-induced apoptotic cells possibly by the interaction of the protein complex causing ubiquitination of the repair proteins.
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