Conserved temporal ordering of promoter activation implicates common mechanisms governing the immediate early response across cell types and stimuli
type: CreativeWork
description: The promoters of immediate early genes (IEGs) are rapidly activated in response to an external stimulus. These genes, also known as primary response genes, have been identified in a range of cell types, under diverse extracellular signals and using varying experimental protocols. Genomic dissection on a case-by-case basis has not resulted in a comprehensive catalogue of IEGs. I completed a rigorous meta-analysis of eight genome-wide FANTOM5 CAGE (cap analysis of gene expression) time-course datasets, and it revealed successive waves of promoter activation in IEGs, recapitulating known relationships between cell types and stimuli. I found a set of 57 (42 protein-coding) candidate IEGs possessing promoters that consistently drive a rapid but transient increase in expression following external stimulation. These genes show significant enrichment for known IEGs reported previously, pathways associated with the immediate early response, and include a number of non-coding RNAs with roles in proliferation and differentiation. There was strong conservation of the ordering of activation for these genes, such that 77 pairwise promoter activation orderings were conserved. Leveraging comprehensive CAGE time series data across cell types, I also observed extensive alternative promoter usage by such genes, which is likely to hinder their discovery from previous, smaller-scale studies. The common activation ordering of the core set of early-responding genes I identified may indicate conserved underlying regulatory mechanisms. By contrast, the considerably larger number of transiently activated genes that are specific to each cell type and stimulus illustrates the breadth of the primary response.
abstract: The promoters of immediate early genes (IEGs) are rapidly activated in response to an external stimulus. These genes, also known as primary response genes, have been identified in a range of cell types, under diverse extracellular signals and using varying experimental protocols. Genomic dissection on a case-by-case basis has not resulted in a comprehensive catalogue of IEGs. I completed a rigorous meta-analysis of eight genome-wide FANTOM5 CAGE (cap analysis of gene expression) time-course datasets, and it revealed successive waves of promoter activation in IEGs, recapitulating known relationships between cell types and stimuli. I found a set of 57 (42 protein-coding) candidate IEGs possessing promoters that consistently drive a rapid but transient increase in expression following external stimulation. These genes show significant enrichment for known IEGs reported previously, pathways associated with the immediate early response, and include a number of non-coding RNAs with roles in proliferation and differentiation. There was strong conservation of the ordering of activation for these genes, such that 77 pairwise promoter activation orderings were conserved. Leveraging comprehensive CAGE time series data across cell types, I also observed extensive alternative promoter usage by such genes, which is likely to hinder their discovery from previous, smaller-scale studies. The common activation ordering of the core set of early-responding genes I identified may indicate conserved underlying regulatory mechanisms. By contrast, the considerably larger number of transiently activated genes that are specific to each cell type and stimulus illustrates the breadth of the primary response.
author: Vacca, Annalaura
language: en
keywords: immediate-early genes, IEGs, FANTOM5 project, XBP1
date published: 2019-12-06
date modified: 2026-07-24T02:13:57Z
provider: University of Edinburgh
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: The University of Edinburgh

PropertyValue
property ID: Handle
value: https://hdl.handle.net/1842/36761

PropertyValue
property ID: DOI
value: 10.7488/era/66