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Whyte, J.J., Zhao, J., Wells, K.D., Samuel, M.S., Whitworth, K.M., Walters, E.M., Laughlin, M.H. and Prathe, R.S. (2011) Gene Targeting with Zinc Finger Nucleases to Produce Cloned eGFP Knockout. Molecular Reproduction Development, 78, 2.
http://dx.doi.org/10.1002/mrd.21271

has been cited by the following article:

• TITLE: Targeted Mutagenesis of Beta-Lactoglobulin Gene in Caprine Fetal Fibroblasts by Context-Dependent Assembly Zinc-Finger Nucleases

  AUTHORS: Yuguo Yuan, Yong Cheng, Jinyu Wang, Qiuling Peng

  KEYWORDS: Context-Dependent Assembly, Zinc Finger Nucleases, Beta-Lactoglobulin, Gene Knockout, Goat

  JOURNAL NAME: Open Access Library Journal, Vol.3 No.7, July 26, 2016

  ABSTRACT: Targeted mutagenesis by zinc-finger nucleases (ZFNs) can be used to generate knock-out mammalian cell lines with high efficiency. A number of different methods have been developed for the design and assembly of gene-specific ZFNs, making them easily accessible to researchers. In this study, we used ZFNs assembled through the CoDA (context-dependent assembly) platforms to generate mutant caprine fetal fibroblasts cells for the BLG gene. ZFN plasmid was introduced into the caprine fetal fibroblasts cell by electroporation. ZFN-induced cleavage of the target sequence was confirmed by the Surveyor nuclease assay analysis. Sequence analysis revealed that ZFN-induced mutations such as base insertion, deletion, or substitution were generated in the ZFN cleavage site of BLG. The simplicity and efficacy of CoDA will enable broad application of ZFN technology. This technique could be used with homologous arm, which may target foreign genes into the BLG locus at higher efficiency.