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Foamy Virus Integrase in Development of Viral Vector for Gene Therapy

Due to the broad host suitability of viral vectors and their high gene delivery capacity, many researchers are focusing on viral vector-mediated gene therapy. Among the retroviruses, foamy viruses have been considered potential gene therapy vectors because of their non-pathogenicity. To date, the pr...

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Detalles Bibliográficos
Autores principales: Kim, Jinsun, Lee, Ga-Eun, Shin, Cha-Gyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Microbiology and Biotechnology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728412/
https://www.ncbi.nlm.nih.gov/pubmed/32699199
http://dx.doi.org/10.4014/jmb.2003.03046
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author Kim, Jinsun
Lee, Ga-Eun
Shin, Cha-Gyun
author_facet Kim, Jinsun
Lee, Ga-Eun
Shin, Cha-Gyun
author_sort Kim, Jinsun
collection PubMed
description Due to the broad host suitability of viral vectors and their high gene delivery capacity, many researchers are focusing on viral vector-mediated gene therapy. Among the retroviruses, foamy viruses have been considered potential gene therapy vectors because of their non-pathogenicity. To date, the prototype foamy virus is the only retrovirus that has a high-resolution structure of intasomes, nucleoprotein complexes formed by integrase, and viral DNA. The integration of viral DNA into the host chromosome is an essential step for viral vector development. This process is mediated by virally encoded integrase, which catalyzes unique chemical reactions. Additionally, recent studies on foamy virus integrase elucidated the catalytic functions of its three distinct domains and their effect on viral pathogenicity. This review focuses on recent advancements in biochemical, structural, and functional studies of foamy virus integrase for gene therapy vector research.
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spelling pubmed-97284122022-12-13 Foamy Virus Integrase in Development of Viral Vector for Gene Therapy Kim, Jinsun Lee, Ga-Eun Shin, Cha-Gyun J Microbiol Biotechnol Review Due to the broad host suitability of viral vectors and their high gene delivery capacity, many researchers are focusing on viral vector-mediated gene therapy. Among the retroviruses, foamy viruses have been considered potential gene therapy vectors because of their non-pathogenicity. To date, the prototype foamy virus is the only retrovirus that has a high-resolution structure of intasomes, nucleoprotein complexes formed by integrase, and viral DNA. The integration of viral DNA into the host chromosome is an essential step for viral vector development. This process is mediated by virally encoded integrase, which catalyzes unique chemical reactions. Additionally, recent studies on foamy virus integrase elucidated the catalytic functions of its three distinct domains and their effect on viral pathogenicity. This review focuses on recent advancements in biochemical, structural, and functional studies of foamy virus integrase for gene therapy vector research. The Korean Society for Microbiology and Biotechnology 2020-09-28 2020-07-14 /pmc/articles/PMC9728412/ /pubmed/32699199 http://dx.doi.org/10.4014/jmb.2003.03046 Text en Copyright © 2020 The Korean Society for Microbiology and Biotechnology https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Kim, Jinsun
Lee, Ga-Eun
Shin, Cha-Gyun
Foamy Virus Integrase in Development of Viral Vector for Gene Therapy
title Foamy Virus Integrase in Development of Viral Vector for Gene Therapy
title_full Foamy Virus Integrase in Development of Viral Vector for Gene Therapy
title_fullStr Foamy Virus Integrase in Development of Viral Vector for Gene Therapy
title_full_unstemmed Foamy Virus Integrase in Development of Viral Vector for Gene Therapy
title_short Foamy Virus Integrase in Development of Viral Vector for Gene Therapy
title_sort foamy virus integrase in development of viral vector for gene therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728412/
https://www.ncbi.nlm.nih.gov/pubmed/32699199
http://dx.doi.org/10.4014/jmb.2003.03046
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