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A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice

Pulsing cellular dynamics in genetic circuits have been shown to provide critical capabilities to cells in stress response, signaling and development. Despite the fascinating discoveries made in the past few years, the mechanisms and functional capabilities of most pulsing systems remain unclear, an...

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Autores principales: Li, Ting, Chen, Xianjun, Qian, Yajie, Shao, Jiawei, Li, Xie, Liu, Shuning, Zhu, Linyong, Zhao, Yuzheng, Ye, Haifeng, Yang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840992/
https://www.ncbi.nlm.nih.gov/pubmed/33504786
http://dx.doi.org/10.1038/s41467-021-20913-1
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author Li, Ting
Chen, Xianjun
Qian, Yajie
Shao, Jiawei
Li, Xie
Liu, Shuning
Zhu, Linyong
Zhao, Yuzheng
Ye, Haifeng
Yang, Yi
author_facet Li, Ting
Chen, Xianjun
Qian, Yajie
Shao, Jiawei
Li, Xie
Liu, Shuning
Zhu, Linyong
Zhao, Yuzheng
Ye, Haifeng
Yang, Yi
author_sort Li, Ting
collection PubMed
description Pulsing cellular dynamics in genetic circuits have been shown to provide critical capabilities to cells in stress response, signaling and development. Despite the fascinating discoveries made in the past few years, the mechanisms and functional capabilities of most pulsing systems remain unclear, and one of the critical challenges is the lack of a technology that allows pulsatile regulation of transgene expression both in vitro and in vivo. Here, we describe the development of a synthetic BRET-based transgene expression (LuminON) system based on a luminescent transcription factor, termed luminGAVPO, by fusing NanoLuc luciferase to the light-switchable transcription factor GAVPO. luminGAVPO allows pulsatile and quantitative activation of transgene expression via both chemogenetic and optogenetic approaches in mammalian cells and mice. Both the pulse amplitude and duration of transgene expression are highly tunable via adjustment of the amount of furimazine. We further demonstrated LuminON-mediated blood-glucose homeostasis in type 1 diabetic mice. We believe that the BRET-based LuminON system with the pulsatile dynamics of transgene expression provides a highly sensitive tool for precise manipulation in biological systems that has strong potential for application in diverse basic biological studies and gene- and cell-based precision therapies in the future.
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spelling pubmed-78409922021-02-08 A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice Li, Ting Chen, Xianjun Qian, Yajie Shao, Jiawei Li, Xie Liu, Shuning Zhu, Linyong Zhao, Yuzheng Ye, Haifeng Yang, Yi Nat Commun Article Pulsing cellular dynamics in genetic circuits have been shown to provide critical capabilities to cells in stress response, signaling and development. Despite the fascinating discoveries made in the past few years, the mechanisms and functional capabilities of most pulsing systems remain unclear, and one of the critical challenges is the lack of a technology that allows pulsatile regulation of transgene expression both in vitro and in vivo. Here, we describe the development of a synthetic BRET-based transgene expression (LuminON) system based on a luminescent transcription factor, termed luminGAVPO, by fusing NanoLuc luciferase to the light-switchable transcription factor GAVPO. luminGAVPO allows pulsatile and quantitative activation of transgene expression via both chemogenetic and optogenetic approaches in mammalian cells and mice. Both the pulse amplitude and duration of transgene expression are highly tunable via adjustment of the amount of furimazine. We further demonstrated LuminON-mediated blood-glucose homeostasis in type 1 diabetic mice. We believe that the BRET-based LuminON system with the pulsatile dynamics of transgene expression provides a highly sensitive tool for precise manipulation in biological systems that has strong potential for application in diverse basic biological studies and gene- and cell-based precision therapies in the future. Nature Publishing Group UK 2021-01-27 /pmc/articles/PMC7840992/ /pubmed/33504786 http://dx.doi.org/10.1038/s41467-021-20913-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Ting
Chen, Xianjun
Qian, Yajie
Shao, Jiawei
Li, Xie
Liu, Shuning
Zhu, Linyong
Zhao, Yuzheng
Ye, Haifeng
Yang, Yi
A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
title A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
title_full A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
title_fullStr A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
title_full_unstemmed A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
title_short A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
title_sort synthetic bret-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840992/
https://www.ncbi.nlm.nih.gov/pubmed/33504786
http://dx.doi.org/10.1038/s41467-021-20913-1
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