Cargando…
OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression
Regulated systems for transgene expression are useful tools in basic research and a promising platform in biomedicine due to their regulated transgene expression by an inducer. The emergence of optogenetics expression systems enabled the construction of light-switchable systems, enhancing the spatia...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253389/ https://www.ncbi.nlm.nih.gov/pubmed/37298488 http://dx.doi.org/10.3390/ijms24119537 |
_version_ | 1785056394283581440 |
---|---|
author | Arancibia, Duxan Pol, Iracy Vargas-Fernández, Martín Zárate, Rafaella V. Signorelli, Janetti R. Zamorano, Pedro |
author_facet | Arancibia, Duxan Pol, Iracy Vargas-Fernández, Martín Zárate, Rafaella V. Signorelli, Janetti R. Zamorano, Pedro |
author_sort | Arancibia, Duxan |
collection | PubMed |
description | Regulated systems for transgene expression are useful tools in basic research and a promising platform in biomedicine due to their regulated transgene expression by an inducer. The emergence of optogenetics expression systems enabled the construction of light-switchable systems, enhancing the spatial and temporal resolution of a transgene. The LightOn system is an optogenetic tool that regulates the expression of a gene of interest using blue light as an inducer. This system is based on a photosensitive protein (GAVPO), which dimerizes and binds to the UASG sequence in response to blue light, triggering the expression of a downstream transgene. Previously, we adapted the LightOn system to a dual lentiviral vector system for neurons. Here, we continue the optimization and assemble all components of the LightOn system into a single lentiviral plasmid, the OPTO-BLUE system. For functional validation, we used enhanced green fluorescent protein (EGFP) as an expression reporter (OPTO-BLUE-EGFP) and evaluated the efficiency of EGFP expression by transfection and transduction in HEK293-T cells exposed to continuous blue-light illumination. Altogether, these results prove that the optimized OPTO-BLUE system allows the light-controlled expression of a reporter protein according to a specific time and light intensity. Likewise, this system should provide an important molecular tool to modulate gene expression of any protein by blue light. |
format | Online Article Text |
id | pubmed-10253389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102533892023-06-10 OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression Arancibia, Duxan Pol, Iracy Vargas-Fernández, Martín Zárate, Rafaella V. Signorelli, Janetti R. Zamorano, Pedro Int J Mol Sci Article Regulated systems for transgene expression are useful tools in basic research and a promising platform in biomedicine due to their regulated transgene expression by an inducer. The emergence of optogenetics expression systems enabled the construction of light-switchable systems, enhancing the spatial and temporal resolution of a transgene. The LightOn system is an optogenetic tool that regulates the expression of a gene of interest using blue light as an inducer. This system is based on a photosensitive protein (GAVPO), which dimerizes and binds to the UASG sequence in response to blue light, triggering the expression of a downstream transgene. Previously, we adapted the LightOn system to a dual lentiviral vector system for neurons. Here, we continue the optimization and assemble all components of the LightOn system into a single lentiviral plasmid, the OPTO-BLUE system. For functional validation, we used enhanced green fluorescent protein (EGFP) as an expression reporter (OPTO-BLUE-EGFP) and evaluated the efficiency of EGFP expression by transfection and transduction in HEK293-T cells exposed to continuous blue-light illumination. Altogether, these results prove that the optimized OPTO-BLUE system allows the light-controlled expression of a reporter protein according to a specific time and light intensity. Likewise, this system should provide an important molecular tool to modulate gene expression of any protein by blue light. MDPI 2023-05-31 /pmc/articles/PMC10253389/ /pubmed/37298488 http://dx.doi.org/10.3390/ijms24119537 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. 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 | Article Arancibia, Duxan Pol, Iracy Vargas-Fernández, Martín Zárate, Rafaella V. Signorelli, Janetti R. Zamorano, Pedro OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression |
title | OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression |
title_full | OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression |
title_fullStr | OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression |
title_full_unstemmed | OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression |
title_short | OPTO-BLUE: An Integrated Bidirectional Optogenetic Lentiviral Platform for Controlled Light-Induced Gene Expression |
title_sort | opto-blue: an integrated bidirectional optogenetic lentiviral platform for controlled light-induced gene expression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253389/ https://www.ncbi.nlm.nih.gov/pubmed/37298488 http://dx.doi.org/10.3390/ijms24119537 |
work_keys_str_mv | AT arancibiaduxan optoblueanintegratedbidirectionaloptogeneticlentiviralplatformforcontrolledlightinducedgeneexpression AT poliracy optoblueanintegratedbidirectionaloptogeneticlentiviralplatformforcontrolledlightinducedgeneexpression AT vargasfernandezmartin optoblueanintegratedbidirectionaloptogeneticlentiviralplatformforcontrolledlightinducedgeneexpression AT zaraterafaellav optoblueanintegratedbidirectionaloptogeneticlentiviralplatformforcontrolledlightinducedgeneexpression AT signorellijanettir optoblueanintegratedbidirectionaloptogeneticlentiviralplatformforcontrolledlightinducedgeneexpression AT zamoranopedro optoblueanintegratedbidirectionaloptogeneticlentiviralplatformforcontrolledlightinducedgeneexpression |