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User-Friendly Genetic Conditional Knockout Strategies by CRISPR/Cas9.
Chen, Liangliang; Ye, Ying; Dai, Hongxia; Zhang, Heyao; Zhang, Xue; Wu, Qiang; Zhu, Zhexin; Spalinskas, Rapolas; Ren, Wenyan; Zhang, Wensheng.
Afiliação
  • Chen L; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
  • Ye Y; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
  • Dai H; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
  • Zhang H; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
  • Zhang X; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
  • Wu Q; The State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Avenida Wai Long, Taipa, Macau.
  • Zhu Z; Department of Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.
  • Spalinskas R; Science for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology, 106 91 Stockholm, Sweden.
  • Ren W; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
  • Zhang W; Cam-Su Genomic Resource Center, Soochow University, Suzhou 215123, China.
Stem Cells Int ; 2018: 9576959, 2018.
Article em En | MEDLINE | ID: mdl-30013601
ABSTRACT
Loss-of-function studies are critically important in gene functional analysis of model organisms and cells. However, conditional gene inactivation in diploid cells is difficult to achieve, as it involves laborious vector construction, multifold electroporation, and complicated genotyping. Here, a strategy is presented for generating biallelic conditional gene and DNA regulatory region knockouts in mouse embryonic stem cells by codelivery of CRISPR-Cas9 and short-homology-arm targeting vectors sequentially or simultaneously. Collectively, a simple and rapid method was presented to knock out any DNA element conditionally. This approach will facilitate the functional studies of essential genes and regulatory regions during development.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Stem Cells Int Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Stem Cells Int Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China