Recent developments and clinical studies utilizing engineered zinc finger nuclease technology

• Published in: Cellular and molecular life sciences : CMLS 2015-10, Vol.72 (20), p.3819-3830
• Main Authors: Jo, Young-Il, Kim, Hyongbum, Ramakrishna, Suresh
• Format: Article
• Language: English
• Subjects: Animals; Animals, Domestic - genetics; Binding sites; Biochemistry; Biomedical and Life Sciences; Biomedicine; Biotechnology; Cell Biology; Cell Culture Techniques; Clinical trials; cold stress; Deoxyribonucleases - chemistry; Deoxyribonucleic acid; DNA; Gene therapy; genes; Genetic disorders; genetic engineering; Genetic Engineering - methods; Genetic Therapy - methods; Genetic Therapy - trends; homologous recombination; humans; Life Sciences; medicine; mutants; nucleases; Review; Zinc; zinc finger motif; Zinc Fingers
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-015-1956-5

Efficient methods for creating targeted genetic modifications have long been sought for the investigation of gene function and the development of therapeutic modalities for various diseases, including genetic disorders. Although such modifications are possible using homologous recombination, the efficiency is extremely low. Zinc finger nucleases (ZFNs) are custom-designed artificial nucleases that make double-strand breaks at specific sequences, enabling efficient targeted genetic modifications such as corrections, additions, gene knockouts and structural variations. ZFNs are composed of two domains: (i) a DNA-binding domain comprised of zinc finger modules and (ii) the FokI nuclease domain that cleaves the DNA strand. Over 17 years after ZFNs were initially developed, a number of improvements have been made. Here, we will review the developments and future perspectives of ZFN technology. For example, ZFN activity and specificity have been significantly enhanced by modifying the DNA-binding domain and FokI cleavage domain. Advances in culture methods, such as the application of a cold shock and the use of small molecules that affect ZFN stability, have also increased ZFN activity. Furthermore, ZFN-induced mutant cells can be enriched using episomal surrogate reporters. Additionally, we discuss several ongoing clinical studies that are based on ZFN-mediated genome editing in humans. These breakthroughs have substantially facilitated the use of ZFNs in research, medicine and biotechnology.