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Large-scale genetic perturbations reveal regulatory networks and an abundance of gene-specific repressors.

TitleLarge-scale genetic perturbations reveal regulatory networks and an abundance of gene-specific repressors.
Publication TypeJournal Article
Year of Publication2014
AuthorsKemmeren P, Sameith K, van de Pasch LAL, Benschop JJ, Lenstra TL, Margaritis T, O'Duibhir E, Apweiler E, van Wageningen S, Ko CW, van Heesch S, Kashani MM, Ampatziadis-Michailidis G, Brok MO, Brabers NACH, Miles AJ, Bouwmeester D, van Hooff SR, van Bakel H, Sluiters E, Bakker LV, Snel B, Lijnzaad P, van Leenen D, Koerkamp MJAGroot, Holstege FCP
JournalCell
Volume157
Issue3
Pagination740-52
Date Published2014 Apr 24
ISSN1097-4172
KeywordsGene Deletion, Gene Expression Regulation, Fungal, Gene Knockout Techniques, Gene Regulatory Networks, Genetic Techniques, Saccharomyces cerevisiae, Transcriptome
Abstract

To understand regulatory systems, it would be useful to uniformly determine how different components contribute to the expression of all other genes. We therefore monitored mRNA expression genome-wide, for individual deletions of one-quarter of yeast genes, focusing on (putative) regulators. The resulting genetic perturbation signatures reflect many different properties. These include the architecture of protein complexes and pathways, identification of expression changes compatible with viability, and the varying responsiveness to genetic perturbation. The data are assembled into a genetic perturbation network that shows different connectivities for different classes of regulators. Four feed-forward loop (FFL) types are overrepresented, including incoherent type 2 FFLs that likely represent feedback. Systematic transcription factor classification shows a surprisingly high abundance of gene-specific repressors, suggesting that yeast chromatin is not as generally restrictive to transcription as is often assumed. The data set is useful for studying individual genes and for discovering properties of an entire regulatory system.

DOI10.1016/j.cell.2014.02.054
Alternate JournalCell
PubMed ID24766815
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