Cargando…

Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors

Significant progress has been made in developing recombinant adeno-associated virus (rAAV) for clinical gene therapy. While rAAV is a versatile gene delivery platform, its packaging limit of 4.7 kb limits the diseases it can target. Here, we report two unusually small promoters that enable the expre...

Descripción completa

Detalles Bibliográficos
Autores principales: Chai, Sunghee, Wakefield, Leslie, Norgard, Mason, Li, Bin, Enicks, David, Marks, Daniel L., Grompe, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241652/
https://www.ncbi.nlm.nih.gov/pubmed/37287749
http://dx.doi.org/10.1016/j.omtm.2023.05.013
_version_ 1785054034491604992
author Chai, Sunghee
Wakefield, Leslie
Norgard, Mason
Li, Bin
Enicks, David
Marks, Daniel L.
Grompe, Markus
author_facet Chai, Sunghee
Wakefield, Leslie
Norgard, Mason
Li, Bin
Enicks, David
Marks, Daniel L.
Grompe, Markus
author_sort Chai, Sunghee
collection PubMed
description Significant progress has been made in developing recombinant adeno-associated virus (rAAV) for clinical gene therapy. While rAAV is a versatile gene delivery platform, its packaging limit of 4.7 kb limits the diseases it can target. Here, we report two unusually small promoters that enable the expression of larger transgenes than standard promoters. These micro-promoters are only 84 (MP-84) and 135 bp (MP-135) in size but have activity in most cells and tissues comparable to the CAG promoter, the strongest ubiquitous promoter to date. MP-84- and MP-135-based rAAV constructs displayed robust activity in cultured cells from the three different germ-layer lineages. In addition, reporter gene expression was documented in human primary hepatocytes and pancreatic islets and in multiple mouse tissues in vivo, including brain and skeletal muscle. MP-84 and MP-135 will enable the therapeutic expression of transgenes currently too large for rAAV vectors.
format Online
Article
Text
id pubmed-10241652
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Society of Gene & Cell Therapy
record_format MEDLINE/PubMed
spelling pubmed-102416522023-06-07 Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors Chai, Sunghee Wakefield, Leslie Norgard, Mason Li, Bin Enicks, David Marks, Daniel L. Grompe, Markus Mol Ther Methods Clin Dev Original Article Significant progress has been made in developing recombinant adeno-associated virus (rAAV) for clinical gene therapy. While rAAV is a versatile gene delivery platform, its packaging limit of 4.7 kb limits the diseases it can target. Here, we report two unusually small promoters that enable the expression of larger transgenes than standard promoters. These micro-promoters are only 84 (MP-84) and 135 bp (MP-135) in size but have activity in most cells and tissues comparable to the CAG promoter, the strongest ubiquitous promoter to date. MP-84- and MP-135-based rAAV constructs displayed robust activity in cultured cells from the three different germ-layer lineages. In addition, reporter gene expression was documented in human primary hepatocytes and pancreatic islets and in multiple mouse tissues in vivo, including brain and skeletal muscle. MP-84 and MP-135 will enable the therapeutic expression of transgenes currently too large for rAAV vectors. American Society of Gene & Cell Therapy 2023-05-17 /pmc/articles/PMC10241652/ /pubmed/37287749 http://dx.doi.org/10.1016/j.omtm.2023.05.013 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chai, Sunghee
Wakefield, Leslie
Norgard, Mason
Li, Bin
Enicks, David
Marks, Daniel L.
Grompe, Markus
Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
title Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
title_full Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
title_fullStr Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
title_full_unstemmed Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
title_short Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
title_sort strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241652/
https://www.ncbi.nlm.nih.gov/pubmed/37287749
http://dx.doi.org/10.1016/j.omtm.2023.05.013
work_keys_str_mv AT chaisunghee strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors
AT wakefieldleslie strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors
AT norgardmason strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors
AT libin strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors
AT enicksdavid strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors
AT marksdaniell strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors
AT grompemarkus strongubiquitousmicropromotersforrecombinantadenoassociatedviralvectors