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In vivo genome editing via CRISPR-Cas9 mediated homology-independent targeted integration

Publicado en: Nature

 

Targeted genome editing via engineered nucleases is an exciting area of biomedical research and holds potential for clinical applications. Despite rapid advances in the field, in vivo targeted transgene integration is still infeasible because current tools are inefficient1, especially for non-dividing cells, which compose most adult tissues. This poses a barrier for uncovering fundamental biological principles and developing treatments for a broad range of genetic disorders2. Based on clustered regularly interspaced short palindromic repeat/Cas9 (CRISPR/Cas9)34 technology, here we devise a homology-independent targeted integration (HITI) strategy, which allows for robust DNA knock-in in both dividing and non-dividing cells in vitro and, more importantly, in vivo (for example, in neurons of postnatal mammals). As a proof of concept of its therapeutic potential, we demonstrate the efficacy of HITI in improving visual function using a rat model of the retinal degeneration condition retinitis pigmentosa. The HITI method presented here establishes new avenues for basic research and targeted gene therapies.

 

Autores:

Suzuki, K., Tsunekawa, Y., Hernandez-Benitez, R., Wu, J., Zhu, J., Kim, E., Hatanaka, F., Yamamoto, M., Araoka, T., Li, Z., Kurita, M., Hishida, T., Li, M., Aizawa, E., Chen, S., Goebl, A., Soligalla, R.D., Qu, J., Jiang, T., Skowronska-Krawczyk, D., Rodriguez Esteban, C., Lajara, J., Nuñez, E., Guillen, P., Campistol, J.M., Matsuzaki, F., Liu, G.-H., Magistretti, P., Zhang, K., Callaway, E., Zhang, K and Izpisua Belmonte, J.C. “In vivo genome editing via CRISPR-Cas9 mediated homology-independent targeted integrationNature 540, 144-149 (01 December 2016).

 

Link: http://www.nature.com/nature/journal/v540/n7631/full/nature20565.html

 

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