期刊文献+

An episomal CRISPR/Cas9 system to derive vector-free gene modified mammalian cells 被引量:1

An episomal CRISPR/Cas9 system to derive vector-free gene modified mammalian cells
原文传递
导出
摘要 Dear Editor,CRISPR and CRISPR-associated (Cas) proteins play their adaptive immunity role in degrading foreign nucleic acids in both bacteria and archaea. CRISPP,/Cas has proved efficient in modifying mammalian genomes (Cong et al., 2013; Mali et al., 2013) and various delivery methods for Cas9: gRNA complex have been established. Among different delivery means, in vitro transcribed Cas9 mRNNgRNA, Dear Editor,CRISPR and CRISPR-associated (Cas) proteins play their adaptive immunity role in degrading foreign nucleic acids in both bacteria and archaea. CRISPP,/Cas has proved efficient in modifying mammalian genomes (Cong et al., 2013; Mali et al., 2013) and various delivery methods for Cas9: gRNA complex have been established. Among different delivery means, in vitro transcribed Cas9 mRNNgRNA,
机构地区 China Agr Univ
出处 《Protein & Cell》 SCIE CAS CSCD 2016年第9期689-691,共3页 蛋白质与细胞(英文版)
  • 相关文献

参考文献10

  • 1Cong L, Ran FA, Cox D, Lin S, Barretto R, Habib N, Hsu PD, Wu X, Jiang W, Marraffini LA et al (2013) Multiplex genome engineering using CRISPR/Cas systems. Science 339:819-823.
  • 2Donsante A, Miller DG, Li Y, Vogler C, Brunt EM, Russell DW, Sands MS (2007) AAV vector integration sites in mouse hepatoceUular carcinoma. Science 317:477.
  • 3Kouranova E, Forbes K, Zhao G, Warren J, Barte}s A, Wu Y, Cui X (2016) CRISPRs for optimal targeting: delivery of CRISPR components as DNA, RNA and protein into cultured cells and single-cell embryos. Hum Gene Ther 27:464-475.
  • 4Li H, Malani N, Hamilton SR, Schlachterman A, Bussadori G, Edmonson SE, Shah R, Arruda VR, Mingozzi F, Wdght JF et al (2011) Assessing the potential for AAV vector genotoxicity in a mudne model. Blood 117:3311-3319.
  • 5Lin S, Staahl BT, Alia RK, Doudna JA (2014) Enhanced homology- directed human genome engineering by controlled timing of CRISPR/Cas9 delivery, eLife 3:e04766.
  • 6Mali P, Yang L, Esvelt KM, Aach J, Guell M, DiCarlo JE, Norville JE, Church GM (2013) RNA-guided human genome engineering via Cas9. Science 339:823-826.
  • 7Nanbo A, Sugden A, Sugden B (2007) The coupling of synthesis and partitioning of EBV's plasmid replicon is revealed in live cells. EMBO J 26:4252-4262.
  • 8Okita K, Matsumura Y, Sato Y, Okada A, Morizane A, Okamoto S, Hong H, Nakagawa M, Tanabe K, Tezuka K et al (2011) A more efficient method to generate integration-free human iPS cells. Nat Methods 8:U409-U452.
  • 9Yin H, Song CQ, Dorkin JR, Zhu L J, Li Y, Wu Q, Park A, Yang J, Suresh S, Bizhanova A et al (2016) Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo. Nat Biotechnol 34:328-333.
  • 10Yu JY, Hu K J, Smuga-Otto K, Tian SL, Stewart R, Slukvin II, Thomson JA (2009) Human induced pluripotent stem cells free of vector and transgene sequences. Science 324:797-801.

同被引文献1

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