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Programmable mammalian translational modulators by CRISPR-associated proteins

Translational modulation based on RNA-binding proteins can be used to construct artificial gene circuits, but RNA-binding proteins capable of regulating translation efficiently and orthogonally remain scarce. Here we report CARTRIDGE (Cas-Responsive Translational Regulation Integratable into Diverse...

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Autores principales: Kawasaki, Shunsuke, Ono, Hiroki, Hirosawa, Moe, Kuwabara, Takeru, Sumi, Shunsuke, Lee, Suji, Woltjen, Knut, Saito, Hirohide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115826/
https://www.ncbi.nlm.nih.gov/pubmed/37076490
http://dx.doi.org/10.1038/s41467-023-37540-7
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author Kawasaki, Shunsuke
Ono, Hiroki
Hirosawa, Moe
Kuwabara, Takeru
Sumi, Shunsuke
Lee, Suji
Woltjen, Knut
Saito, Hirohide
author_facet Kawasaki, Shunsuke
Ono, Hiroki
Hirosawa, Moe
Kuwabara, Takeru
Sumi, Shunsuke
Lee, Suji
Woltjen, Knut
Saito, Hirohide
author_sort Kawasaki, Shunsuke
collection PubMed
description Translational modulation based on RNA-binding proteins can be used to construct artificial gene circuits, but RNA-binding proteins capable of regulating translation efficiently and orthogonally remain scarce. Here we report CARTRIDGE (Cas-Responsive Translational Regulation Integratable into Diverse Gene control) to repurpose Cas proteins as translational modulators in mammalian cells. We demonstrate that a set of Cas proteins efficiently and orthogonally repress or activate the translation of designed mRNAs that contain a Cas-binding RNA motif in the 5’-UTR. By linking multiple Cas-mediated translational modulators, we designed and built artificial circuits like logic gates, cascades, and half-subtractor circuits. Moreover, we show that various CRISPR-related technologies like anti-CRISPR and split-Cas9 platforms could be similarly repurposed to control translation. Coupling Cas-mediated translational and transcriptional regulation enhanced the complexity of synthetic circuits built by only introducing a few additional elements. Collectively, CARTRIDGE has enormous potential as a versatile molecular toolkit for mammalian synthetic biology.
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spelling pubmed-101158262023-04-21 Programmable mammalian translational modulators by CRISPR-associated proteins Kawasaki, Shunsuke Ono, Hiroki Hirosawa, Moe Kuwabara, Takeru Sumi, Shunsuke Lee, Suji Woltjen, Knut Saito, Hirohide Nat Commun Article Translational modulation based on RNA-binding proteins can be used to construct artificial gene circuits, but RNA-binding proteins capable of regulating translation efficiently and orthogonally remain scarce. Here we report CARTRIDGE (Cas-Responsive Translational Regulation Integratable into Diverse Gene control) to repurpose Cas proteins as translational modulators in mammalian cells. We demonstrate that a set of Cas proteins efficiently and orthogonally repress or activate the translation of designed mRNAs that contain a Cas-binding RNA motif in the 5’-UTR. By linking multiple Cas-mediated translational modulators, we designed and built artificial circuits like logic gates, cascades, and half-subtractor circuits. Moreover, we show that various CRISPR-related technologies like anti-CRISPR and split-Cas9 platforms could be similarly repurposed to control translation. Coupling Cas-mediated translational and transcriptional regulation enhanced the complexity of synthetic circuits built by only introducing a few additional elements. Collectively, CARTRIDGE has enormous potential as a versatile molecular toolkit for mammalian synthetic biology. Nature Publishing Group UK 2023-04-19 /pmc/articles/PMC10115826/ /pubmed/37076490 http://dx.doi.org/10.1038/s41467-023-37540-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kawasaki, Shunsuke
Ono, Hiroki
Hirosawa, Moe
Kuwabara, Takeru
Sumi, Shunsuke
Lee, Suji
Woltjen, Knut
Saito, Hirohide
Programmable mammalian translational modulators by CRISPR-associated proteins
title Programmable mammalian translational modulators by CRISPR-associated proteins
title_full Programmable mammalian translational modulators by CRISPR-associated proteins
title_fullStr Programmable mammalian translational modulators by CRISPR-associated proteins
title_full_unstemmed Programmable mammalian translational modulators by CRISPR-associated proteins
title_short Programmable mammalian translational modulators by CRISPR-associated proteins
title_sort programmable mammalian translational modulators by crispr-associated proteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115826/
https://www.ncbi.nlm.nih.gov/pubmed/37076490
http://dx.doi.org/10.1038/s41467-023-37540-7
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