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Tunable Temperature-Sensitive Transcriptional Activation Based on Lambda Repressor
[Image: see text] Temperature is a versatile input signal for the control of engineered cellular functions. Sharp induction of gene expression with heat has been established using bacteria- and phage-derived temperature-sensitive transcriptional repressors with tunable switching temperatures. Howeve...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295150/ https://www.ncbi.nlm.nih.gov/pubmed/35708251 http://dx.doi.org/10.1021/acssynbio.2c00093 |
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author | Xiong, Lealia L. Garrett, Michael A. Buss, Marjorie T. Kornfield, Julia A. Shapiro, Mikhail G. |
author_facet | Xiong, Lealia L. Garrett, Michael A. Buss, Marjorie T. Kornfield, Julia A. Shapiro, Mikhail G. |
author_sort | Xiong, Lealia L. |
collection | PubMed |
description | [Image: see text] Temperature is a versatile input signal for the control of engineered cellular functions. Sharp induction of gene expression with heat has been established using bacteria- and phage-derived temperature-sensitive transcriptional repressors with tunable switching temperatures. However, few temperature-sensitive transcriptional activators have been reported that enable direct gene induction with cooling. Such activators would expand the application space for temperature control. In this technical note, we show that temperature-dependent versions of the Lambda phage repressor CI can serve as tunable cold-actuated transactivators. Natively, CI serves as both a repressor and activator of transcription. Previously, thermolabile mutants of CI, known as the TcI family, were used to repress the cognate promoters PR and PL. We hypothesized that TcI mutants can also serve as temperature-sensitive activators of transcription at CI’s natural PRM promoter, creating cold-inducible operons with a tunable response to temperature. Indeed, we demonstrate temperature-responsive activation by two variants of TcI with set points at 35.5 and 38.5 °C in E. coli. In addition, we show that TcI can serve as both an activator and a repressor of different genes in the same genetic circuit, leading to opposite thermal responses. Transcriptional activation by TcI expands the toolbox for control of cellular function using globally or locally applied thermal inputs. |
format | Online Article Text |
id | pubmed-9295150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92951502022-07-20 Tunable Temperature-Sensitive Transcriptional Activation Based on Lambda Repressor Xiong, Lealia L. Garrett, Michael A. Buss, Marjorie T. Kornfield, Julia A. Shapiro, Mikhail G. ACS Synth Biol [Image: see text] Temperature is a versatile input signal for the control of engineered cellular functions. Sharp induction of gene expression with heat has been established using bacteria- and phage-derived temperature-sensitive transcriptional repressors with tunable switching temperatures. However, few temperature-sensitive transcriptional activators have been reported that enable direct gene induction with cooling. Such activators would expand the application space for temperature control. In this technical note, we show that temperature-dependent versions of the Lambda phage repressor CI can serve as tunable cold-actuated transactivators. Natively, CI serves as both a repressor and activator of transcription. Previously, thermolabile mutants of CI, known as the TcI family, were used to repress the cognate promoters PR and PL. We hypothesized that TcI mutants can also serve as temperature-sensitive activators of transcription at CI’s natural PRM promoter, creating cold-inducible operons with a tunable response to temperature. Indeed, we demonstrate temperature-responsive activation by two variants of TcI with set points at 35.5 and 38.5 °C in E. coli. In addition, we show that TcI can serve as both an activator and a repressor of different genes in the same genetic circuit, leading to opposite thermal responses. Transcriptional activation by TcI expands the toolbox for control of cellular function using globally or locally applied thermal inputs. American Chemical Society 2022-06-16 2022-07-15 /pmc/articles/PMC9295150/ /pubmed/35708251 http://dx.doi.org/10.1021/acssynbio.2c00093 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Xiong, Lealia L. Garrett, Michael A. Buss, Marjorie T. Kornfield, Julia A. Shapiro, Mikhail G. Tunable Temperature-Sensitive Transcriptional Activation Based on Lambda Repressor |
title | Tunable Temperature-Sensitive Transcriptional Activation
Based on Lambda Repressor |
title_full | Tunable Temperature-Sensitive Transcriptional Activation
Based on Lambda Repressor |
title_fullStr | Tunable Temperature-Sensitive Transcriptional Activation
Based on Lambda Repressor |
title_full_unstemmed | Tunable Temperature-Sensitive Transcriptional Activation
Based on Lambda Repressor |
title_short | Tunable Temperature-Sensitive Transcriptional Activation
Based on Lambda Repressor |
title_sort | tunable temperature-sensitive transcriptional activation
based on lambda repressor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295150/ https://www.ncbi.nlm.nih.gov/pubmed/35708251 http://dx.doi.org/10.1021/acssynbio.2c00093 |
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