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Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs
by
Merrill, Collin B.
, Pabon, Miguel A.
, Montgomery, Austin B.
, Shabalin, Andrey A.
, Rodan, Aylin R.
, Rothenfluh, Adrian
in
Accessibility
/ Animal Genetics and Genomics
/ Animals
/ Annotations
/ Assaying
/ ATAC-seq
/ Binding sites
/ Biomedical and Life Sciences
/ Cellular communication
/ Chromatin
/ Chromatin - genetics
/ Chromatin Immunoprecipitation Sequencing
/ Datasets
/ DNA sequencing
/ Drosophila - genetics
/ Drosophila melanogaster
/ Enhancers
/ Gene expression
/ Gene regulation
/ Genetic aspects
/ Genomes
/ Genomics
/ Health aspects
/ High-Throughput Nucleotide Sequencing
/ Insects
/ Insulin
/ Insulin - pharmacology
/ Life Sciences
/ Methods
/ Microarrays
/ Microbial Genetics and Genomics
/ Next-generation sequencing
/ Nucleotide sequencing
/ Plant Genetics and Genomics
/ Proteomics
/ Reporter gene
/ Ribonucleic acid
/ RNA
/ RNA-seq
/ S2 cells
/ Signal transduction
/ Transposase
/ Transposases - genetics
2022
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Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs
by
Merrill, Collin B.
, Pabon, Miguel A.
, Montgomery, Austin B.
, Shabalin, Andrey A.
, Rodan, Aylin R.
, Rothenfluh, Adrian
in
Accessibility
/ Animal Genetics and Genomics
/ Animals
/ Annotations
/ Assaying
/ ATAC-seq
/ Binding sites
/ Biomedical and Life Sciences
/ Cellular communication
/ Chromatin
/ Chromatin - genetics
/ Chromatin Immunoprecipitation Sequencing
/ Datasets
/ DNA sequencing
/ Drosophila - genetics
/ Drosophila melanogaster
/ Enhancers
/ Gene expression
/ Gene regulation
/ Genetic aspects
/ Genomes
/ Genomics
/ Health aspects
/ High-Throughput Nucleotide Sequencing
/ Insects
/ Insulin
/ Insulin - pharmacology
/ Life Sciences
/ Methods
/ Microarrays
/ Microbial Genetics and Genomics
/ Next-generation sequencing
/ Nucleotide sequencing
/ Plant Genetics and Genomics
/ Proteomics
/ Reporter gene
/ Ribonucleic acid
/ RNA
/ RNA-seq
/ S2 cells
/ Signal transduction
/ Transposase
/ Transposases - genetics
2022
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Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs
by
Merrill, Collin B.
, Pabon, Miguel A.
, Montgomery, Austin B.
, Shabalin, Andrey A.
, Rodan, Aylin R.
, Rothenfluh, Adrian
in
Accessibility
/ Animal Genetics and Genomics
/ Animals
/ Annotations
/ Assaying
/ ATAC-seq
/ Binding sites
/ Biomedical and Life Sciences
/ Cellular communication
/ Chromatin
/ Chromatin - genetics
/ Chromatin Immunoprecipitation Sequencing
/ Datasets
/ DNA sequencing
/ Drosophila - genetics
/ Drosophila melanogaster
/ Enhancers
/ Gene expression
/ Gene regulation
/ Genetic aspects
/ Genomes
/ Genomics
/ Health aspects
/ High-Throughput Nucleotide Sequencing
/ Insects
/ Insulin
/ Insulin - pharmacology
/ Life Sciences
/ Methods
/ Microarrays
/ Microbial Genetics and Genomics
/ Next-generation sequencing
/ Nucleotide sequencing
/ Plant Genetics and Genomics
/ Proteomics
/ Reporter gene
/ Ribonucleic acid
/ RNA
/ RNA-seq
/ S2 cells
/ Signal transduction
/ Transposase
/ Transposases - genetics
2022
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Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs
Journal Article
Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs
2022
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Overview
Background
Gene regulation is critical for proper cellular function. Next-generation sequencing technology has revealed the presence of regulatory networks that regulate gene expression and essential cellular functions. Studies investigating the epigenome have begun to uncover the complex mechanisms regulating transcription. Assay for transposase-accessible chromatin by sequencing (ATAC-seq) is quickly becoming the assay of choice for many epigenomic investigations. However, whether intervention-mediated changes in accessible chromatin determined by ATAC-seq can be harnessed to generate intervention-inducible reporter constructs has not been systematically assayed.
Results
We used the insulin signaling pathway as a model to investigate chromatin regions and gene expression changes using ATAC- and RNA-seq in insulin-treated
Drosophila
S2 cells. We found correlations between ATAC- and RNA-seq data, especially when stratifying differentially-accessible chromatin regions by annotated feature type. In particular, our data demonstrated a weak but significant correlation between chromatin regions annotated to enhancers (1-2 kb from the transcription start site) and downstream gene expression. We cloned candidate enhancer regions upstream of luciferase and demonstrate insulin-inducibility of several of these reporters.
Conclusions
Insulin-induced chromatin accessibility determined by ATAC-seq reveals enhancer regions that drive insulin-inducible reporter gene expression.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
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