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Engineered systems of inducible anti-repressors for the next generation of biological programming
Traditionally engineered genetic circuits have almost exclusively used naturally occurring transcriptional repressors. Recently, non-natural transcription factors (repressors) have been engineered and employed in synthetic biology with great success. However, transcriptional anti-repressors have lar...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477573/ https://www.ncbi.nlm.nih.gov/pubmed/32895374 http://dx.doi.org/10.1038/s41467-020-18302-1 |
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author | Groseclose, Thomas M. Rondon, Ronald E. Herde, Zachary D. Aldrete, Carlos A. Wilson, Corey J. |
author_facet | Groseclose, Thomas M. Rondon, Ronald E. Herde, Zachary D. Aldrete, Carlos A. Wilson, Corey J. |
author_sort | Groseclose, Thomas M. |
collection | PubMed |
description | Traditionally engineered genetic circuits have almost exclusively used naturally occurring transcriptional repressors. Recently, non-natural transcription factors (repressors) have been engineered and employed in synthetic biology with great success. However, transcriptional anti-repressors have largely been absent with regard to the regulation of genes in engineered genetic circuits. Here, we present a workflow for engineering systems of non-natural anti-repressors. In this study, we create 41 inducible anti-repressors. This collection of transcription factors respond to two distinct ligands, fructose (anti-FruR) or D-ribose (anti-RbsR); and were complemented by 14 additional engineered anti-repressors that respond to the ligand isopropyl β-d-1-thiogalactopyranoside (anti-LacI). In turn, we use this collection of anti-repressors and complementary genetic architectures to confer logical control over gene expression. Here, we achieved all NOT oriented logical controls (i.e., NOT, NOR, NAND, and XNOR). The engineered transcription factors and corresponding series, parallel, and series-parallel genetic architectures represent a nascent anti-repressor based transcriptional programming structure. |
format | Online Article Text |
id | pubmed-7477573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74775732020-09-21 Engineered systems of inducible anti-repressors for the next generation of biological programming Groseclose, Thomas M. Rondon, Ronald E. Herde, Zachary D. Aldrete, Carlos A. Wilson, Corey J. Nat Commun Article Traditionally engineered genetic circuits have almost exclusively used naturally occurring transcriptional repressors. Recently, non-natural transcription factors (repressors) have been engineered and employed in synthetic biology with great success. However, transcriptional anti-repressors have largely been absent with regard to the regulation of genes in engineered genetic circuits. Here, we present a workflow for engineering systems of non-natural anti-repressors. In this study, we create 41 inducible anti-repressors. This collection of transcription factors respond to two distinct ligands, fructose (anti-FruR) or D-ribose (anti-RbsR); and were complemented by 14 additional engineered anti-repressors that respond to the ligand isopropyl β-d-1-thiogalactopyranoside (anti-LacI). In turn, we use this collection of anti-repressors and complementary genetic architectures to confer logical control over gene expression. Here, we achieved all NOT oriented logical controls (i.e., NOT, NOR, NAND, and XNOR). The engineered transcription factors and corresponding series, parallel, and series-parallel genetic architectures represent a nascent anti-repressor based transcriptional programming structure. Nature Publishing Group UK 2020-09-07 /pmc/articles/PMC7477573/ /pubmed/32895374 http://dx.doi.org/10.1038/s41467-020-18302-1 Text en © The Author(s) 2020 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 Groseclose, Thomas M. Rondon, Ronald E. Herde, Zachary D. Aldrete, Carlos A. Wilson, Corey J. Engineered systems of inducible anti-repressors for the next generation of biological programming |
title | Engineered systems of inducible anti-repressors for the next generation of biological programming |
title_full | Engineered systems of inducible anti-repressors for the next generation of biological programming |
title_fullStr | Engineered systems of inducible anti-repressors for the next generation of biological programming |
title_full_unstemmed | Engineered systems of inducible anti-repressors for the next generation of biological programming |
title_short | Engineered systems of inducible anti-repressors for the next generation of biological programming |
title_sort | engineered systems of inducible anti-repressors for the next generation of biological programming |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477573/ https://www.ncbi.nlm.nih.gov/pubmed/32895374 http://dx.doi.org/10.1038/s41467-020-18302-1 |
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