Detecting Differential Transcription Factor Activity from ATAC-Seq Data

Transcription factors are managers of the cellular factory, and key components to many diseases. Many non-coding single nucleotide polymorphisms affect transcription factors, either by directly altering the protein or its functional activity at individual binding sites. Here we first briefly summari...

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Main Authors: Ignacio J. Tripodi, Mary A. Allen, Robin D. Dowell
Format: Article
Language:English
Published: MDPI AG 2018-05-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/23/5/1136
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author Ignacio J. Tripodi
Mary A. Allen
Robin D. Dowell
author_facet Ignacio J. Tripodi
Mary A. Allen
Robin D. Dowell
author_sort Ignacio J. Tripodi
collection DOAJ
description Transcription factors are managers of the cellular factory, and key components to many diseases. Many non-coding single nucleotide polymorphisms affect transcription factors, either by directly altering the protein or its functional activity at individual binding sites. Here we first briefly summarize high-throughput approaches to studying transcription factor activity. We then demonstrate, using published chromatin accessibility data (specifically ATAC-seq), that the genome-wide profile of TF recognition motifs relative to regions of open chromatin can determine the key transcription factor altered by a perturbation. Our method of determining which TFs are altered by a perturbation is simple, is quick to implement, and can be used when biological samples are limited. In the future, we envision that this method could be applied to determine which TFs show altered activity in response to a wide variety of drugs and diseases.
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spelling doaj.art-0f75646673bd4064844333c3f560b2cc2022-12-21T19:33:41ZengMDPI AGMolecules1420-30492018-05-01235113610.3390/molecules23051136molecules23051136Detecting Differential Transcription Factor Activity from ATAC-Seq DataIgnacio J. Tripodi0Mary A. Allen1Robin D. Dowell2Computer Science, University of Colorado, Boulder, CO 80305, USABioFrontiers Institute, University of Colorado, Boulder, CO 80303, USAComputer Science, University of Colorado, Boulder, CO 80305, USATranscription factors are managers of the cellular factory, and key components to many diseases. Many non-coding single nucleotide polymorphisms affect transcription factors, either by directly altering the protein or its functional activity at individual binding sites. Here we first briefly summarize high-throughput approaches to studying transcription factor activity. We then demonstrate, using published chromatin accessibility data (specifically ATAC-seq), that the genome-wide profile of TF recognition motifs relative to regions of open chromatin can determine the key transcription factor altered by a perturbation. Our method of determining which TFs are altered by a perturbation is simple, is quick to implement, and can be used when biological samples are limited. In the future, we envision that this method could be applied to determine which TFs show altered activity in response to a wide variety of drugs and diseases.http://www.mdpi.com/1420-3049/23/5/1136transcription factorperturbationRNA-seqDNase I cleavageATAC-seqopen chromatinmotifDAStk
spellingShingle Ignacio J. Tripodi
Mary A. Allen
Robin D. Dowell
Detecting Differential Transcription Factor Activity from ATAC-Seq Data
Molecules
transcription factor
perturbation
RNA-seq
DNase I cleavage
ATAC-seq
open chromatin
motif
DAStk
title Detecting Differential Transcription Factor Activity from ATAC-Seq Data
title_full Detecting Differential Transcription Factor Activity from ATAC-Seq Data
title_fullStr Detecting Differential Transcription Factor Activity from ATAC-Seq Data
title_full_unstemmed Detecting Differential Transcription Factor Activity from ATAC-Seq Data
title_short Detecting Differential Transcription Factor Activity from ATAC-Seq Data
title_sort detecting differential transcription factor activity from atac seq data
topic transcription factor
perturbation
RNA-seq
DNase I cleavage
ATAC-seq
open chromatin
motif
DAStk
url http://www.mdpi.com/1420-3049/23/5/1136
work_keys_str_mv AT ignaciojtripodi detectingdifferentialtranscriptionfactoractivityfromatacseqdata
AT maryaallen detectingdifferentialtranscriptionfactoractivityfromatacseqdata
AT robinddowell detectingdifferentialtranscriptionfactoractivityfromatacseqdata