期刊文献+

靶向人Ku70 mRNA反义核苷酸的优化设计与筛选

Design and selection of antisense nucleotide targeting on human Ku70 mRNA
下载PDF
导出
摘要 目的:联合应用RNAdraw和Sfold软件设计并筛选低毒且高效抑制Hela细胞Ku70 mRNA表达的反义寡核苷酸。方法:从GenBank获得人Ku70 mRNA全序列,联合应用RNAdraw与Sfold软件,根据最小自由能原理设计多条20 nt的反义寡核苷酸,脂质体转染后MTT法检测其非序列特异性细胞毒性,选择毒性最小者并转染Hela细胞,RT-PCR检测转染前后Ku70 mRNA的表达水平并进行比较。结果:靶向Ku70 mRNA设计6条20 nt的反义寡核苷酸,其中NO.1序列非特异性毒性最低,对Hela细胞的生长抑制率(50、100和200 nmol.L-1浓度组分别为4.8%、9.5%和10.2%)与脂质体组比较差异无显著性(P>0.05),用毒性最低序列转染Hela细胞后使Ku70 mRNA表达水平显著降低(P<0.01),条带强度和面积与未转染组比较分别下降81.6%和77.6%。结论:联合应用计算机软件RNAdraw和Sfold对设计反义核酸有较大的指导意义,能实现较高的命中率,设计的反义寡核苷酸能有效抑制Hela细胞Ku70mRNA的表达。
出处 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2007年第6期1094-1097,共4页 Journal of Jilin University:Medicine Edition
基金 吉林省科技厅资助课题(20051004-1)
  • 相关文献

参考文献10

  • 1Branch AD. A good antisense molecule is hard to find[J]. TiBS, 1998, 23: 45-50.
  • 2储淳,罗天学.反义核酸的骨架修饰及其应用[J].国外医学(分子生物学分册),2000,22(2):115-120. 被引量:4
  • 3Sanna MG, Correia JDS, Ducrey O, et al. IAP Suppression of apoptosis involves distinct mechanisms: the TAK1/JNK1 signaling cascade and caspase inhibition[J]. Mol Cell Biol, 2002, 22 (6): 1754- 1766.
  • 4萨姆布鲁克J 拉塞尔DW.黄培堂 王嘉玺 朱厚础 等译.分子克隆实验指南[M]第3版[M].北京:科学出版社,2002.8..
  • 5Yuen AR, Sidic BI. Clinical studies of antisense therapy in cancer [J]. Front Biosci, 2000, 26 (5): 588-593.
  • 6Crook NE, Clem RJ, Miller LK. An apoptosis inhibiting baculovirus gene with a zinc finger-like motif [J]. J Virol, 1993, 67 (4): 2168-2174.
  • 7袁守军,汤仲明.反义药物药理学的研究进展[J].国外医学(药学分册),1998,25(5):257-261. 被引量:4
  • 8Ma H, Thibault J, Lu Y, et al. The development and applications of nonradioactive plate-formatted DNA-binding assay for KuT0/80, a multifunctional DNA-binding protein complex [J]. Assay Drug Dev Technol, 2004, 2 (5):483- 495.
  • 9张懿玮,徐明.Ku70的多样性功能及研究展望[J].国外医学(遗传学分册),2004,27(5):282-285. 被引量:4
  • 10孙丽君,张梅,郑英.氯丙嗪对体外培养人宫颈癌Hela细胞株的生长抑制作用[J].郑州大学学报(医学版),2005,40(2):344-345. 被引量:7

二级参考文献46

  • 1温汉平,王小宁.肿瘤细胞体外药敏试验MTT分析法[J].中华肿瘤杂志,1993,15(6):470-471. 被引量:63
  • 2Matheos D, Ruiz MT, Price GB, et al. Ku antigen, an origin-specific binding protein that associates with replication proteins, is required for mammalian DNA replication. Biochim Biophys Acta, 2002, 1578 (1-3): 59-72.
  • 3Takata M, Sasaki MS, Sonoda E, et al. Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells. EMBO J, 1998, 17(18): 5497-550
  • 4Adachi N, Ishino T, Ishii Y, et al. DNAligase Ⅳ-deficient cells are more resistant to ionizing radiation in the absence of Ku70: Implications for DNA double-strand break repair. Proc Natl Acad Sci USA,2001, 98(21): 12109-12113.
  • 5Karmakar P, Snowden CM, Ramsden DA, et al. Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus. Nucleic Acids Res, 2002, 30 (16):3583-3591.
  • 6Wang J, Dong X, Myung K, et al. Identification of two domains of the p70 Ku protein mediating dimerization with p80 and DNA binding. J Biol Chem, 1998, 273(2): 842-848.
  • 7Featherstone C, Jackson SP. Ku,a DNA repair protein with multiple cellular functions? Mutat Res, 1999, 434(1): 3-15.
  • 8Ruiz MT, Nichols A, Price GB, et al. DNA-PKcs-OBA/Ku associate in the absence of DNA, as revealed by two-dimensional capillary gel electromobility shift assay. Electrophoresis, 2002, 23(15): 2485-2489.
  • 9Willis DM, Loewy AP, Charlton-Kachigian N, et al. Regulation of osteocalcin gene expression by a novel Ku antigen transcription factor complex. J Biol Chem, 2002, 277(40): 37280-37291.
  • 10Tang D, Xie Y, Zhao M, et al. Repression of the HSP70B promoter by NFIL6, Ku70, and MAPK involves three complementary mechanisms. Biochem Biophys Res Commun, 2001, 280(1): 280-285.

共引文献128

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部