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A modular open platform for systematic functional studies under physiological conditions

Any profound comprehension of gene function requires detailed information about the subcellular localization, molecular interactions and spatio-temporal dynamics of gene products. We developed a multifunctional integrase (MIN) tag for rapid and versatile genome engineering that serves not only as a...

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Autores principales: Mulholland, Christopher B., Smets, Martha, Schmidtmann, Elisabeth, Leidescher, Susanne, Markaki, Yolanda, Hofweber, Mario, Qin, Weihua, Manzo, Massimiliano, Kremmer, Elisabeth, Thanisch, Katharina, Bauer, Christina, Rombaut, Pascaline, Herzog, Franz, Leonhardt, Heinrich, Bultmann, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787826/
https://www.ncbi.nlm.nih.gov/pubmed/26007658
http://dx.doi.org/10.1093/nar/gkv550
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author Mulholland, Christopher B.
Smets, Martha
Schmidtmann, Elisabeth
Leidescher, Susanne
Markaki, Yolanda
Hofweber, Mario
Qin, Weihua
Manzo, Massimiliano
Kremmer, Elisabeth
Thanisch, Katharina
Bauer, Christina
Rombaut, Pascaline
Herzog, Franz
Leonhardt, Heinrich
Bultmann, Sebastian
author_facet Mulholland, Christopher B.
Smets, Martha
Schmidtmann, Elisabeth
Leidescher, Susanne
Markaki, Yolanda
Hofweber, Mario
Qin, Weihua
Manzo, Massimiliano
Kremmer, Elisabeth
Thanisch, Katharina
Bauer, Christina
Rombaut, Pascaline
Herzog, Franz
Leonhardt, Heinrich
Bultmann, Sebastian
author_sort Mulholland, Christopher B.
collection PubMed
description Any profound comprehension of gene function requires detailed information about the subcellular localization, molecular interactions and spatio-temporal dynamics of gene products. We developed a multifunctional integrase (MIN) tag for rapid and versatile genome engineering that serves not only as a genetic entry site for the Bxb1 integrase but also as a novel epitope tag for standardized detection and precipitation. For the systematic study of epigenetic factors, including Dnmt1, Dnmt3a, Dnmt3b, Tet1, Tet2, Tet3 and Uhrf1, we generated MIN-tagged embryonic stem cell lines and created a toolbox of prefabricated modules that can be integrated via Bxb1-mediated recombination. We used these functional modules to study protein interactions and their spatio-temporal dynamics as well as gene expression and specific mutations during cellular differentiation and in response to external stimuli. Our genome engineering strategy provides a versatile open platform for efficient generation of multiple isogenic cell lines to study gene function under physiological conditions.
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spelling pubmed-47878262016-03-14 A modular open platform for systematic functional studies under physiological conditions Mulholland, Christopher B. Smets, Martha Schmidtmann, Elisabeth Leidescher, Susanne Markaki, Yolanda Hofweber, Mario Qin, Weihua Manzo, Massimiliano Kremmer, Elisabeth Thanisch, Katharina Bauer, Christina Rombaut, Pascaline Herzog, Franz Leonhardt, Heinrich Bultmann, Sebastian Nucleic Acids Res Methods Online Any profound comprehension of gene function requires detailed information about the subcellular localization, molecular interactions and spatio-temporal dynamics of gene products. We developed a multifunctional integrase (MIN) tag for rapid and versatile genome engineering that serves not only as a genetic entry site for the Bxb1 integrase but also as a novel epitope tag for standardized detection and precipitation. For the systematic study of epigenetic factors, including Dnmt1, Dnmt3a, Dnmt3b, Tet1, Tet2, Tet3 and Uhrf1, we generated MIN-tagged embryonic stem cell lines and created a toolbox of prefabricated modules that can be integrated via Bxb1-mediated recombination. We used these functional modules to study protein interactions and their spatio-temporal dynamics as well as gene expression and specific mutations during cellular differentiation and in response to external stimuli. Our genome engineering strategy provides a versatile open platform for efficient generation of multiple isogenic cell lines to study gene function under physiological conditions. Oxford University Press 2015-09-30 2015-05-24 /pmc/articles/PMC4787826/ /pubmed/26007658 http://dx.doi.org/10.1093/nar/gkv550 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Mulholland, Christopher B.
Smets, Martha
Schmidtmann, Elisabeth
Leidescher, Susanne
Markaki, Yolanda
Hofweber, Mario
Qin, Weihua
Manzo, Massimiliano
Kremmer, Elisabeth
Thanisch, Katharina
Bauer, Christina
Rombaut, Pascaline
Herzog, Franz
Leonhardt, Heinrich
Bultmann, Sebastian
A modular open platform for systematic functional studies under physiological conditions
title A modular open platform for systematic functional studies under physiological conditions
title_full A modular open platform for systematic functional studies under physiological conditions
title_fullStr A modular open platform for systematic functional studies under physiological conditions
title_full_unstemmed A modular open platform for systematic functional studies under physiological conditions
title_short A modular open platform for systematic functional studies under physiological conditions
title_sort modular open platform for systematic functional studies under physiological conditions
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787826/
https://www.ncbi.nlm.nih.gov/pubmed/26007658
http://dx.doi.org/10.1093/nar/gkv550
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