Publication:
The IS2 Element Improves Transcription Efficiency of Integration-Deficient Lentiviral Vector Episomes.

dc.contributor.authorSánchez-Hernández, Sabina
dc.contributor.authorGutierrez-Guerrero, Alejandra
dc.contributor.authorMartín-Guerra, Rocío
dc.contributor.authorCortijo-Gutierrez, Marina
dc.contributor.authorTristán-Manzano, María
dc.contributor.authorRodriguez-Perales, Sandra
dc.contributor.authorSanchez, Laura
dc.contributor.authorGarcia-Perez, Jose Luis
dc.contributor.authorChato-Astrain, Jesus
dc.contributor.authorFernandez-Valades, Ricardo
dc.contributor.authorCarrillo-Galvez, Ana Belén
dc.contributor.authorAnderson, Per
dc.contributor.authorMontes, Rosa
dc.contributor.authorReal, Pedro J
dc.contributor.authorMartin, Francisco
dc.contributor.authorBenabdellah, Karim
dc.date.accessioned2023-01-25T10:22:17Z
dc.date.available2023-01-25T10:22:17Z
dc.date.issued2018-08-18
dc.description.abstractIntegration-defective lentiviral vectors (IDLVs) have become an important alternative tool for gene therapy applications and basic research. Unfortunately, IDLVs show lower transgene expression as compared to their integrating counterparts. In this study, we aimed to improve the expression levels of IDLVs by inserting the IS2 element, which harbors SARs and HS4 sequences, into their LTRs (SE-IS2-IDLVs). Contrary to our expectations, the presence of the IS2 element did not abrogate epigenetic silencing by histone deacetylases. In addition, the IS2 element reduced episome levels in IDLV-transduced cells. Interestingly, despite these negative effects, SE-IS2-IDLVs outperformed SE-IDLVs in terms of percentage and expression levels of the transgene in several cell lines, including neurons, neuronal progenitor cells, and induced pluripotent stem cells. We estimated that the IS2 element enhances the transcriptional activity of IDLV LTR circles 6- to 7-fold. The final effect the IS2 element in IDLVs will greatly depend on the target cell and the balance between the negative versus the positive effects of the IS2 element in each cell type. The better performance of SE-IS2-IDLVs was not due to improved stability or differences in the proportions of 1-LTR versus 2-LTR circles but probably to a re-positioning of IS2-episomes into transcriptionally active regions.
dc.identifier.doi10.1016/j.omtn.2018.08.007
dc.identifier.issn2162-2531
dc.identifier.pmcPMC6141704
dc.identifier.pmid30227274
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141704/pdf
dc.identifier.unpaywallURLhttps://www.cell.com/molecular-therapy-family/nucleic-acids/pdf/S2162-2531(18)30212-9.pdf
dc.identifier.urihttp://hdl.handle.net/10668/12961
dc.journal.titleMolecular therapy. Nucleic acids
dc.journal.titleabbreviationMol Ther Nucleic Acids
dc.language.isoen
dc.organizationHospital Universitario Virgen de las Nieves
dc.organizationCentro Pfizer-Universidad de Granada-Junta de Andalucía de Genómica e Investigación Oncológica-GENYO
dc.page.number16-28
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectHS4 insulator
dc.subjectIDLV
dc.subjectgene therapy
dc.subjectlentiviral vector
dc.subjectscaffold or matrix attachment regions
dc.titleThe IS2 Element Improves Transcription Efficiency of Integration-Deficient Lentiviral Vector Episomes.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number13
dspace.entity.typePublication

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