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Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software

Much is still not understood about how gene regulatory interactions control cell fate decisions in single cells, in part due to the difficulty of directly observing gene regulatory processes in vivo. We introduce here a novel integrated setup consisting of a microfluidic chip and accompanying analys...

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Autores principales: Kaiser, Matthias, Jug, Florian, Julou, Thomas, Deshpande, Siddharth, Pfohl, Thomas, Silander, Olin K., Myers, Gene, van Nimwegen, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768764/
https://www.ncbi.nlm.nih.gov/pubmed/29335514
http://dx.doi.org/10.1038/s41467-017-02505-0
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author Kaiser, Matthias
Jug, Florian
Julou, Thomas
Deshpande, Siddharth
Pfohl, Thomas
Silander, Olin K.
Myers, Gene
van Nimwegen, Erik
author_facet Kaiser, Matthias
Jug, Florian
Julou, Thomas
Deshpande, Siddharth
Pfohl, Thomas
Silander, Olin K.
Myers, Gene
van Nimwegen, Erik
author_sort Kaiser, Matthias
collection PubMed
description Much is still not understood about how gene regulatory interactions control cell fate decisions in single cells, in part due to the difficulty of directly observing gene regulatory processes in vivo. We introduce here a novel integrated setup consisting of a microfluidic chip and accompanying analysis software that enable long-term quantitative tracking of growth and gene expression in single cells. The dual-input Mother Machine (DIMM) chip enables controlled and continuous variation of external conditions, allowing direct observation of gene regulatory responses to changing conditions in single cells. The Mother Machine Analyzer (MoMA) software achieves unprecedented accuracy in segmenting and tracking cells, and streamlines high-throughput curation with a novel leveraged editing procedure. We demonstrate the power of the method by uncovering several novel features of an iconic gene regulatory program: the induction of Escherichia coli’s lac operon in response to a switch from glucose to lactose.
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spelling pubmed-57687642018-01-19 Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software Kaiser, Matthias Jug, Florian Julou, Thomas Deshpande, Siddharth Pfohl, Thomas Silander, Olin K. Myers, Gene van Nimwegen, Erik Nat Commun Article Much is still not understood about how gene regulatory interactions control cell fate decisions in single cells, in part due to the difficulty of directly observing gene regulatory processes in vivo. We introduce here a novel integrated setup consisting of a microfluidic chip and accompanying analysis software that enable long-term quantitative tracking of growth and gene expression in single cells. The dual-input Mother Machine (DIMM) chip enables controlled and continuous variation of external conditions, allowing direct observation of gene regulatory responses to changing conditions in single cells. The Mother Machine Analyzer (MoMA) software achieves unprecedented accuracy in segmenting and tracking cells, and streamlines high-throughput curation with a novel leveraged editing procedure. We demonstrate the power of the method by uncovering several novel features of an iconic gene regulatory program: the induction of Escherichia coli’s lac operon in response to a switch from glucose to lactose. Nature Publishing Group UK 2018-01-15 /pmc/articles/PMC5768764/ /pubmed/29335514 http://dx.doi.org/10.1038/s41467-017-02505-0 Text en © The Author(s) 2018 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
Kaiser, Matthias
Jug, Florian
Julou, Thomas
Deshpande, Siddharth
Pfohl, Thomas
Silander, Olin K.
Myers, Gene
van Nimwegen, Erik
Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
title Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
title_full Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
title_fullStr Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
title_full_unstemmed Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
title_short Monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
title_sort monitoring single-cell gene regulation under dynamically controllable conditions with integrated microfluidics and software
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768764/
https://www.ncbi.nlm.nih.gov/pubmed/29335514
http://dx.doi.org/10.1038/s41467-017-02505-0
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