中华放射医学与防护杂志
中華放射醫學與防護雜誌
중화방사의학여방호잡지
Chinese Journal of Radiological Medicine and Protection
2010年
5期
510-512
,共3页
朱应葆%韩云%孙艳%梁莉%贾廷珍
硃應葆%韓雲%孫豔%樑莉%賈廷珍
주응보%한운%손염%량리%가정진
细胞凋亡%HLTF%RING结构域
細胞凋亡%HLTF%RING結構域
세포조망%HLTF%RING결구역
Apoptosis%Helicase-like transcription factor (HLTF)%RING domain
目的 探讨人类解旋酶样转录因子(HLTF)转染对辐射诱导细胞凋亡时DNA修复相关蛋白水平的影响.方法 将野生型和RING结构域突变型HLTF分别转染人肺癌细胞A549,60Coγ射线15 Gy照射诱导细胞凋亡,用Western blot检测HRAD17和HRAD52蛋白水平的变化,免疫共沉淀检测特定复合物的存在.结果 γ射线诱导细胞凋亡时,野生型HLTF转染组与对照组相比,DNA修复蛋白HRAD17和HRAD52水平明显降低,而RING结构域突变组与对照组相比则没有明显变化;辐射诱导细胞凋亡时,HLTF可与HRAD17和HRAD52形成复合物.结论 HLTF可介导辐射诱导的凋亡细胞中HRAD17和HRAD52的降解,其机制可能是通过蛋白质复合物的相互作用使DNA修复蛋白泛素化而降解.
目的 探討人類解鏇酶樣轉錄因子(HLTF)轉染對輻射誘導細胞凋亡時DNA脩複相關蛋白水平的影響.方法 將野生型和RING結構域突變型HLTF分彆轉染人肺癌細胞A549,60Coγ射線15 Gy照射誘導細胞凋亡,用Western blot檢測HRAD17和HRAD52蛋白水平的變化,免疫共沉澱檢測特定複閤物的存在.結果 γ射線誘導細胞凋亡時,野生型HLTF轉染組與對照組相比,DNA脩複蛋白HRAD17和HRAD52水平明顯降低,而RING結構域突變組與對照組相比則沒有明顯變化;輻射誘導細胞凋亡時,HLTF可與HRAD17和HRAD52形成複閤物.結論 HLTF可介導輻射誘導的凋亡細胞中HRAD17和HRAD52的降解,其機製可能是通過蛋白質複閤物的相互作用使DNA脩複蛋白汎素化而降解.
목적 탐토인류해선매양전록인자(HLTF)전염대복사유도세포조망시DNA수복상관단백수평적영향.방법 장야생형화RING결구역돌변형HLTF분별전염인폐암세포A549,60Coγ사선15 Gy조사유도세포조망,용Western blot검측HRAD17화HRAD52단백수평적변화,면역공침정검측특정복합물적존재.결과 γ사선유도세포조망시,야생형HLTF전염조여대조조상비,DNA수복단백HRAD17화HRAD52수평명현강저,이RING결구역돌변조여대조조상비칙몰유명현변화;복사유도세포조망시,HLTF가여HRAD17화HRAD52형성복합물.결론 HLTF가개도복사유도적조망세포중HRAD17화HRAD52적강해,기궤제가능시통과단백질복합물적상호작용사DNA수복단백범소화이강해.
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.