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SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics
Transcription factors (TFs) alter gene expression in response to changes in the environment through sequence-specific interactions with the DNA. These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from l...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024299/ https://www.ncbi.nlm.nih.gov/pubmed/27628341 http://dx.doi.org/10.1038/srep33351 |
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author | Chen, Dana Orenstein, Yaron Golodnitsky, Rada Pellach, Michal Avrahami, Dorit Wachtel, Chaim Ovadia-Shochat, Avital Shir-Shapira, Hila Kedmi, Adi Juven-Gershon, Tamar Shamir, Ron Gerber, Doron |
author_facet | Chen, Dana Orenstein, Yaron Golodnitsky, Rada Pellach, Michal Avrahami, Dorit Wachtel, Chaim Ovadia-Shochat, Avital Shir-Shapira, Hila Kedmi, Adi Juven-Gershon, Tamar Shamir, Ron Gerber, Doron |
author_sort | Chen, Dana |
collection | PubMed |
description | Transcription factors (TFs) alter gene expression in response to changes in the environment through sequence-specific interactions with the DNA. These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from limited dynamic range, sequence bias, lack of specificity and limited throughput. We have developed a microfluidic-based device for SELEX Affinity Landscape MAPping (SELMAP) of TF binding, which allows high-throughput measurement of 16 proteins in parallel. We used it to measure the relative affinities of Pho4, AtERF2 and Btd full-length proteins to millions of different DNA binding sites, and detected both high and low-affinity interactions in equilibrium conditions, generating a comprehensive landscape of the relative TF affinities to all possible DNA 6-mers, and even DNA10-mers with increased sequencing depth. Low quantities of both the TFs and DNA oligomers were sufficient for obtaining high-quality results, significantly reducing experimental costs. SELMAP allows in-depth screening of hundreds of TFs, and provides a means for better understanding of the regulatory processes that govern gene expression. |
format | Online Article Text |
id | pubmed-5024299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50242992016-09-20 SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics Chen, Dana Orenstein, Yaron Golodnitsky, Rada Pellach, Michal Avrahami, Dorit Wachtel, Chaim Ovadia-Shochat, Avital Shir-Shapira, Hila Kedmi, Adi Juven-Gershon, Tamar Shamir, Ron Gerber, Doron Sci Rep Article Transcription factors (TFs) alter gene expression in response to changes in the environment through sequence-specific interactions with the DNA. These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from limited dynamic range, sequence bias, lack of specificity and limited throughput. We have developed a microfluidic-based device for SELEX Affinity Landscape MAPping (SELMAP) of TF binding, which allows high-throughput measurement of 16 proteins in parallel. We used it to measure the relative affinities of Pho4, AtERF2 and Btd full-length proteins to millions of different DNA binding sites, and detected both high and low-affinity interactions in equilibrium conditions, generating a comprehensive landscape of the relative TF affinities to all possible DNA 6-mers, and even DNA10-mers with increased sequencing depth. Low quantities of both the TFs and DNA oligomers were sufficient for obtaining high-quality results, significantly reducing experimental costs. SELMAP allows in-depth screening of hundreds of TFs, and provides a means for better understanding of the regulatory processes that govern gene expression. Nature Publishing Group 2016-09-15 /pmc/articles/PMC5024299/ /pubmed/27628341 http://dx.doi.org/10.1038/srep33351 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Dana Orenstein, Yaron Golodnitsky, Rada Pellach, Michal Avrahami, Dorit Wachtel, Chaim Ovadia-Shochat, Avital Shir-Shapira, Hila Kedmi, Adi Juven-Gershon, Tamar Shamir, Ron Gerber, Doron SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
title | SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
title_full | SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
title_fullStr | SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
title_full_unstemmed | SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
title_short | SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
title_sort | selmap - selex affinity landscape mapping of transcription factor binding sites using integrated microfluidics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024299/ https://www.ncbi.nlm.nih.gov/pubmed/27628341 http://dx.doi.org/10.1038/srep33351 |
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