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Gene Insertion Into Genomic Safe Harbors for Human Gene Therapy

Journal

MOLECULAR THERAPY
Volume 24, Issue 4, Pages 678-684

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/mt.2016.38

Keywords

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Funding

  1. NIH [R00 DK087923, R01 HL121570]
  2. Lawrence Ellison Foundation
  3. Damon Runyon Cancer Research Foundation
  4. Federal Ministry of Education and Research (BMBF)
  5. Deutsche Forschungsgemeinschaft [SFB738]
  6. European Union
  7. Federal Ministry of Education and Research (network project ReGene)
  8. Federal Ministry of Education and Research (network project PidNet)
  9. Federal Ministry of Education and Research (network project IFB-Tx)

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Genomic safe harbors (GSHs) are sites in the genome able to accommodate the integration of new genetic material in a manner that ensures that the newly inserted genetic elements: (i) function predictably and (ii) do not cause alterations of the host genome posing a risk to the host cell or organism. GSHs are thus ideal sites for transgene insertion whose use can empower functional genetics studies in basic research and therapeutic applications in human gene therapy. Currently, no fully validated GSHs exist in the human genome. Here, we review our formerly proposed GSH criteria and discuss additional considerations on extending these criteria, on strategies for the identification and validation of GSHs, as well as future prospects on GSH targeting for therapeutic applications. In view of recent advances in genome biology, gene targeting technologies, and regenerative medicine, gene insertion into GSHs can potentially catalyze nearly all applications in human gene therapy.

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