Skip to content

A summarizing analysis of Fkh1,2 target genes as indicated by 6 ChIP binding studies and an overexpression and deletion study | https://doi.org/10.1016/j.csbj.2022.03.033

Notifications You must be signed in to change notification settings

barberislab/Forkhead-mediated_regulation

Folders and files

NameName
Last commit message
Last commit date

Latest commit

 

History

4 Commits
 
 
 
 
 
 
 
 
 
 
 
 

Repository files navigation

Unveiling Forkhead-mediated regulation of yeast cell cycle and metabolic networks

This is the code repository for the computational analyses featured in:

Matteo Barberis, Thierry D.G.A. Mondeel, Unveiling Forkhead-mediated regulation of yeast cell cycle and metabolic networks, Computational and Structural Biotechnology Journal, 2022.

See https://doi.org/10.1016/j.csbj.2022.03.033 for the full publication.

Abstract

Transcription factors are regulators of the cell’s genomic landscape. By switching single genes or entire molecular pathways on or off, transcription factors modulate the precise timing of their activation. The Forkhead (Fkh) transcription factors are evolutionarily conserved to regulate organismal physiology and cell division. In addition to molecular biology and biochemical efforts, genome-wide studies have been conducted to characterize the genomic landscape potentially regulated by Forkheads in eukaryotes. Here, we discuss and interpret findings reported in six genome-wide Chromatin ImmunoPrecipitation (ChIP) studies, with a particular focus on ChIP-chip and ChIP-exo. We highlight their power and challenges to address Forkhead-mediated regulation of the cellular landscape in budding yeast. Expression changes of the targets identified in the binding assays are investigated by taking expression data for Forkhead deletion and overexpression into account. Forkheads are revealed as regulators of the metabolic network through which cell cycle dynamics may be temporally coordinated further, in addition to their well-known role as regulators of the gene cluster responsible for cell division.

Keywords: Systems biology; Networks; Transcriptional regulation; Forkhead transcription factors; Cell cycle; Metabolism

Releases

No releases published

Packages

No packages published