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An alternative novel tool for DNA editing without target sequence limitation: the structure-guided nuclease

Engineered endonucleases are a powerful tool for editing DNA. However, sequence preferences may limit their application. We engineer a structure-guided endonuclease (SGN) composed of flap endonuclease-1 (FEN-1), which recognizes the 3′ flap structure, and the cleavage domain of Fok I (Fn1), which cl...

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Detalles Bibliográficos
Autores principales: Xu, Shu, Cao, Shasha, Zou, Bingjie, Yue, Yunyun, Gu, Chun, Chen, Xin, Wang, Pei, Dong, Xiaohua, Xiang, Zheng, Li, Kai, Zhu, Minsheng, Zhao, Qingshun, Zhou, Guohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025552/
https://www.ncbi.nlm.nih.gov/pubmed/27634179
http://dx.doi.org/10.1186/s13059-016-1038-5
Descripción
Sumario:Engineered endonucleases are a powerful tool for editing DNA. However, sequence preferences may limit their application. We engineer a structure-guided endonuclease (SGN) composed of flap endonuclease-1 (FEN-1), which recognizes the 3′ flap structure, and the cleavage domain of Fok I (Fn1), which cleaves DNA strands. The SGN recognizes the target DNA on the basis of the 3′ flap structure formed between the target and the guide DNA (gDNA) and cut the target through its Fn1 dimerization. Our results show that the SGN, guided by a pair of gDNAs, cleaves transgenic reporter gene and endogenous genes in zebrafish embryonic genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1038-5) contains supplementary material, which is available to authorized users.