高级检索
马爱国, 刘四朝, 杜卫. 核酸内切酶在DNA断裂损伤检测中的应用研究[J]. 中国公共卫生, 2000, 16(2): 145-146. DOI: 10.11847/zgggws2000-16-02-42
引用本文: 马爱国, 刘四朝, 杜卫. 核酸内切酶在DNA断裂损伤检测中的应用研究[J]. 中国公共卫生, 2000, 16(2): 145-146. DOI: 10.11847/zgggws2000-16-02-42
Ma Aiguo, . Application of Endonuclease to Detecting the Strand Breaks of DNA Oxidative Damage[J]. Chinese Journal of Public Health, 2000, 16(2): 145-146. DOI: 10.11847/zgggws2000-16-02-42
Citation: Ma Aiguo, . Application of Endonuclease to Detecting the Strand Breaks of DNA Oxidative Damage[J]. Chinese Journal of Public Health, 2000, 16(2): 145-146. DOI: 10.11847/zgggws2000-16-02-42

核酸内切酶在DNA断裂损伤检测中的应用研究

Application of Endonuclease to Detecting the Strand Breaks of DNA Oxidative Damage

  • 摘要: 利用人体淋巴细胞和Hela细胞并经100μMH2O2诱导DNA损伤,然后分为对照组和实验组,后者补充25μl-1μg/ml的核酸内切酶Ⅲ.结果显示对照组淋巴细胞经4h培养后DNA断裂损伤下降到63.85(专用单位);补充核酸内切酶Ⅲ的实验组DNA断裂损伤明显增加达到161.93(P<0.05).对照组Hela细胞培养4h后DNA断裂损伤为19,而实验组断裂损伤明显高于对照组达到172.1(P<0.01).提示实验组DNA断裂损伤的增高可能包括H2O2所致DNA直接断裂和核酸内切酶Ⅲ切除修复过程中所形成的修复性断裂两部分,反映了DNA总体损伤水平.

     

    Abstract: The damaged lymphocytes and Hela cells were divided into control groups and supplemental groups treated with 25μl of 1μl/ml endonuclease.The results showed that the damage of DNA strand breaks of lympnocytes was much lower in control with 63.85 arbitary units(AU)than supplement group about 161.93 after 4 hour culture(P<0.05).The similar result was found in Hela cells.The DNA strand breaks were significantly increased from 19.0 in control group to 172.1 in suppiement groups(P<0.01)after 4 hour culture.It was indicated that the supplementation of endonuclease played an important role in the base incision repair and produced a lot of strand breaks from enzymic incision for DNA repair.

     

/

返回文章
返回