Literature DB >> 24766815

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

Patrick Kemmeren1, Katrin Sameith1, Loes A L van de Pasch1, Joris J Benschop1, Tineke L Lenstra1, Thanasis Margaritis1, Eoghan O'Duibhir1, Eva Apweiler1, Sake van Wageningen1, Cheuk W Ko1, Sebastiaan van Heesch1, Mehdi M Kashani1, Giannis Ampatziadis-Michailidis1, Mariel O Brok1, Nathalie A C H Brabers1, Anthony J Miles1, Diane Bouwmeester1, Sander R van Hooff1, Harm van Bakel1, Erik Sluiters1, Linda V Bakker1, Berend Snel2, Philip Lijnzaad1, Dik van Leenen1, Marian J A Groot Koerkamp1, Frank C P Holstege3.   

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.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24766815     DOI: 10.1016/j.cell.2014.02.054

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


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