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Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens

Gene-centered yeast one-hybrid (Y1H) screens provide a powerful and effective strategy to identify transcription factor (TF)-promoter interactions. While genome-wide TF ORFeome clone collections are increasingly available, screening protocols have limitations inherent to the properties of the enzyma...

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Detalles Bibliográficos
Autores principales: Bonaldi, Katia, Li, Zheng, Kang, S. Earl, Breton, Ghislain, Pruneda-Paz, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737895/
https://www.ncbi.nlm.nih.gov/pubmed/28985361
http://dx.doi.org/10.1093/nar/gkx682
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author Bonaldi, Katia
Li, Zheng
Kang, S. Earl
Breton, Ghislain
Pruneda-Paz, Jose L.
author_facet Bonaldi, Katia
Li, Zheng
Kang, S. Earl
Breton, Ghislain
Pruneda-Paz, Jose L.
author_sort Bonaldi, Katia
collection PubMed
description Gene-centered yeast one-hybrid (Y1H) screens provide a powerful and effective strategy to identify transcription factor (TF)-promoter interactions. While genome-wide TF ORFeome clone collections are increasingly available, screening protocols have limitations inherent to the properties of the enzymatic reaction used to identify interactions and to the procedure required to perform the assay in a high-throughput format. Here, we present the development and validation of a streamlined strategy for quantitative and fully automated gene-centered Y1H screens using a novel cell surface Gaussia luciferase reporter.
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spelling pubmed-57378952018-01-04 Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens Bonaldi, Katia Li, Zheng Kang, S. Earl Breton, Ghislain Pruneda-Paz, Jose L. Nucleic Acids Res Methods Online Gene-centered yeast one-hybrid (Y1H) screens provide a powerful and effective strategy to identify transcription factor (TF)-promoter interactions. While genome-wide TF ORFeome clone collections are increasingly available, screening protocols have limitations inherent to the properties of the enzymatic reaction used to identify interactions and to the procedure required to perform the assay in a high-throughput format. Here, we present the development and validation of a streamlined strategy for quantitative and fully automated gene-centered Y1H screens using a novel cell surface Gaussia luciferase reporter. Oxford University Press 2017-10-13 2017-07-31 /pmc/articles/PMC5737895/ /pubmed/28985361 http://dx.doi.org/10.1093/nar/gkx682 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, 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
Bonaldi, Katia
Li, Zheng
Kang, S. Earl
Breton, Ghislain
Pruneda-Paz, Jose L.
Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
title Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
title_full Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
title_fullStr Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
title_full_unstemmed Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
title_short Novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
title_sort novel cell surface luciferase reporter for high-throughput yeast one-hybrid screens
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737895/
https://www.ncbi.nlm.nih.gov/pubmed/28985361
http://dx.doi.org/10.1093/nar/gkx682
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