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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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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. |
format | Online Article Text |
id | pubmed-5737895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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