HK022 bacteriophage integrase mediated RMCE as a potential tool for human gene therapy

Amer Elias, Hala Kassis, Suha Abd Elkader, Natasha Gritsenko, Alessio Nahmad, Hodaya Shir, Liana Younis, Atheer Shannan, Hideki Aihara, Gali Prag, Ezra Yagil, Mikhail Kolot

Research output: Contribution to journalArticlepeer-review

Abstract

HK022 coliphage site-specific recombinase Integrase (Int) can catalyze integrative site-specific recombination and recombinase-mediated cassette exchange (RMCE) reactions in mammalian cell cultures. Owing to the promiscuity of the 7 bp overlap sequence in its att sites, active 'attB' sites flanking human deleterious mutations were previously identified that may serve as substrates for RMCE reactions for future potential gene therapy. However, the wild type Int proved inefficient in catalyzing such RMCE reactions. To address this low efficiency, variants of Int were constructed and examined by integrative site-specific recombination and RMCE assays in human cells using native 'attB' sites. As a proof of concept, various Int derivatives have demonstrated successful RMCE reactions using a pair of native 'attB' sites that were inserted as a substrate into the human genome. Moreover, successful RMCE reactions were demonstrated in native locations of the human CTNS and DMD genes whose mutations are responsible for Cystinosis and Duchene Muscular Dystrophy diseases, respectively. This work provides a steppingstone for potential downstream therapeutic applications.

Original languageEnglish (US)
Pages (from-to)12804-12816
Number of pages13
JournalNucleic acids research
Volume48
Issue number22
DOIs
StatePublished - Dec 16 2020

Bibliographical note

Publisher Copyright:
© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

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