Engineering and optimising deaminase fusions for genome editing
Precision genome engineering using homology donors and the endogenous DNA break repair machinery and recently CRISPR-Cas9 targeted APOBECs have been demonstrated. Here the authors design zinc-finger and TALE chimeric deaminases and investigate editing efficiency and off-target effects.
Guardado en:
Autores principales: | Luhan Yang, Adrian W. Briggs, Wei Leong Chew, Prashant Mali, Marc Guell, John Aach, Daniel Bryan Goodman, David Cox, Yinan Kan, Emal Lesha, Venkataramanan Soundararajan, Feng Zhang, George Church |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2016
|
Materias: | |
Acceso en línea: | https://doaj.org/article/46f1a4a987da4603908d6583916fecd1 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Correction: Corrigendum: Engineering and optimising deaminase fusions for genome editing
por: Luhan Yang, et al.
Publicado: (2017) -
Mitochondrial DNA editing in mice with DddA-TALE fusion deaminases
por: Hyunji Lee, et al.
Publicado: (2021) -
Optimising the utility of pleural fluid adenosine deaminase for the diagnosis of tuberculous pleural effusion
por: Nai-Chien Huan, et al.
Publicado: (2021) -
Expanding C–T base editing toolkit with diversified cytidine deaminases
por: Tian-Lin Cheng, et al.
Publicado: (2019) -
Deaminase-independent inhibition of parvoviruses by the APOBEC3A cytidine deaminase.
por: Iñigo Narvaiza, et al.
Publicado: (2009)