期刊文献+

CRISPR系统的优势与瑕疵 被引量:1

The Advantage and Disadvantage of the CRISPR System
下载PDF
导出
摘要 CRISPR(Clustered Regularly Interspersed Short Palindromic Repeats)系统是一种细菌和古细菌用于对外源遗传物质进行降解的适应性免疫防御机制。其在基因组编辑方面的应用有着比其他核酸内切酶如锌指核酸酶(Zinc Finger Endonuclease,ZFNs)和类转录激活因子效应物核酸酶(Transcription Activator-like Effector Nuclease,TALENs)更好的功能。本文对该系统的分子机理、优势及仍然存在的问题进行阐述。随着对其研究的深入,该技术必将充分发挥其优势,在生命科学的发展中起到重要作用。 The CRISPR(Clustered Regularly Interspersed Short Palindromic Repeats)system comes from bacteria and archaea, which used in the degradation of foreign genetic material asadaptive immune defense mechanism. It is better than ZFN(Zinc Finger Nuclease) and TALENs(Transcription Activator-like Effector Nuclease) applied in the field of genomeediting. In this paper, we summarized the molecular mechanism, advantageand, disadvantage of the CRISPR system. We believe that with the development, this technology will play an important role in the modern life science.
作者 李丹丹 林峻
出处 《生物化工》 2017年第2期73-79,共7页 Biological Chemical Engineering
关键词 CRISPR系统 基因组编辑 ZFNs TALENs CRISPR system Genome editing ZFNs TALENs
  • 相关文献

参考文献7

二级参考文献73

  • 1王军,郑增忍,王晶钰.动物源性食品中沙门氏菌的风险评估[J].中国动物检疫,2007,24(4):23-25. 被引量:102
  • 2[1]PASTWA E,BLASIAK J.Non-homologous DNA end joining[J].Acta Biochimica Polonica,2003,50 (4):891-908.
  • 3[2]MICHAEL R L,YUNMEI M,ULRICH P,et al.The mechanism vertebrate non-homologous DNA end joining and its role in V(D)J recombination[J].DNA Rep,2004,3(8):817-826.
  • 4[3]FISHEL R,WILSON T.Muts homologs in mammalian cells[J].Curr Op Gen,1997,Dev (7):105-113.
  • 5[4]O CONNOR T R,LAVAL F.Isolation and structure of a cDNA expressing a mammalian 3-methyladenime-DNA glycosylase[J].EMBO J,1990,9:3334-3337.
  • 6[5]CRAIG H,FREDERICK W A.The cellular response to general and proammed DNA double strand breaks[J].DNA Rep,2004,3:781-796.
  • 7[6]WETERINGS E,DIK C,GENT V.The mechanism of non-homologous end joining:A synopsis of synapsis[J].DNA Rep,2004,3:1425-1435.
  • 8[7]PIERCE A J,HU P,HAN M,et al.Ku DNA end-binding protein modulates homologous repair of double-strand breaks in mammalian cells[J].Genes Dev,2001,5:3237-3242.
  • 9[8]WALKER J R,CORPINA R A,GOLDBERG J,et al.Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair[J].Nature,2001,412:606-614.
  • 10[9]SUSAN MB,MARK AB,JAMES H,et al.The kinase activity of DNA-PK is reqired to protect mammalian telomeres[J].DNA Repair,2004,3:225-233.

共引文献338

同被引文献30

引证文献1

二级引证文献1

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