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Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae

This work describes the development and characterization of a modular synthetic expression system that provides a broad range of adjustable and predictable expression levels in S. cerevisiae. The system works as a fixed-gain transcription amplifier, where the input signal is transferred via a synthe...

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Autores principales: Rantasalo, Anssi, Czeizler, Elena, Virtanen, Riitta, Rousu, Juho, Lähdesmäki, Harri, Penttilä, Merja, Jäntti, Jussi, Mojzita, Dominik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762949/
https://www.ncbi.nlm.nih.gov/pubmed/26901642
http://dx.doi.org/10.1371/journal.pone.0148320
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author Rantasalo, Anssi
Czeizler, Elena
Virtanen, Riitta
Rousu, Juho
Lähdesmäki, Harri
Penttilä, Merja
Jäntti, Jussi
Mojzita, Dominik
author_facet Rantasalo, Anssi
Czeizler, Elena
Virtanen, Riitta
Rousu, Juho
Lähdesmäki, Harri
Penttilä, Merja
Jäntti, Jussi
Mojzita, Dominik
author_sort Rantasalo, Anssi
collection PubMed
description This work describes the development and characterization of a modular synthetic expression system that provides a broad range of adjustable and predictable expression levels in S. cerevisiae. The system works as a fixed-gain transcription amplifier, where the input signal is transferred via a synthetic transcription factor (sTF) onto a synthetic promoter, containing a defined core promoter, generating a transcription output signal. The system activation is based on the bacterial LexA-DNA-binding domain, a set of modified, modular LexA-binding sites and a selection of transcription activation domains. We show both experimentally and computationally that the tuning of the system is achieved through the selection of three separate modules, each of which enables an adjustable output signal: 1) the transcription-activation domain of the sTF, 2) the binding-site modules in the output promoter, and 3) the core promoter modules which define the transcription initiation site in the output promoter. The system has a novel bidirectional architecture that enables generation of compact, yet versatile expression modules for multiple genes with highly diversified expression levels ranging from negligible to very strong using one synthetic transcription factor. In contrast to most existing modular gene expression regulation systems, the present system is independent from externally added compounds. Furthermore, the established system was minimally affected by the several tested growth conditions. These features suggest that it can be highly useful in large scale biotechnology applications.
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spelling pubmed-47629492016-03-07 Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae Rantasalo, Anssi Czeizler, Elena Virtanen, Riitta Rousu, Juho Lähdesmäki, Harri Penttilä, Merja Jäntti, Jussi Mojzita, Dominik PLoS One Research Article This work describes the development and characterization of a modular synthetic expression system that provides a broad range of adjustable and predictable expression levels in S. cerevisiae. The system works as a fixed-gain transcription amplifier, where the input signal is transferred via a synthetic transcription factor (sTF) onto a synthetic promoter, containing a defined core promoter, generating a transcription output signal. The system activation is based on the bacterial LexA-DNA-binding domain, a set of modified, modular LexA-binding sites and a selection of transcription activation domains. We show both experimentally and computationally that the tuning of the system is achieved through the selection of three separate modules, each of which enables an adjustable output signal: 1) the transcription-activation domain of the sTF, 2) the binding-site modules in the output promoter, and 3) the core promoter modules which define the transcription initiation site in the output promoter. The system has a novel bidirectional architecture that enables generation of compact, yet versatile expression modules for multiple genes with highly diversified expression levels ranging from negligible to very strong using one synthetic transcription factor. In contrast to most existing modular gene expression regulation systems, the present system is independent from externally added compounds. Furthermore, the established system was minimally affected by the several tested growth conditions. These features suggest that it can be highly useful in large scale biotechnology applications. Public Library of Science 2016-02-22 /pmc/articles/PMC4762949/ /pubmed/26901642 http://dx.doi.org/10.1371/journal.pone.0148320 Text en © 2016 Rantasalo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rantasalo, Anssi
Czeizler, Elena
Virtanen, Riitta
Rousu, Juho
Lähdesmäki, Harri
Penttilä, Merja
Jäntti, Jussi
Mojzita, Dominik
Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae
title Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae
title_full Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae
title_fullStr Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae
title_full_unstemmed Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae
title_short Synthetic Transcription Amplifier System for Orthogonal Control of Gene Expression in Saccharomyces cerevisiae
title_sort synthetic transcription amplifier system for orthogonal control of gene expression in saccharomyces cerevisiae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762949/
https://www.ncbi.nlm.nih.gov/pubmed/26901642
http://dx.doi.org/10.1371/journal.pone.0148320
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