Issue 1, 2009

Transcriptional control of the quorum sensing response in yeast

Abstract

Quorum sensing is a process of intercellular communication. It allows individual cells to assess population density and to co-ordinate behaviour by secreting and sensing communication molecules. In the yeast Saccharomyces cerevisiae, the communication molecules are the aromatic alcoholstryptophol and phenylethanol, and quorum sensing regulates the transition between the solitary yeast form and the filamentous form. Though it is known that addition of these communication molecules to yeast cultures causes large changes in gene expression, how these changes are orchestrated and whether this system is conserved in related fungal species is still unknown. In this work, by employing an integrated computational approach that makes use of large-scale genomics datasets, such as ChIP-ChIP and expression analysis upon deletion and over-expression of transcriptional factors, we predict CAT8 and MIG1 as key transcriptional regulators that control the differential expression of the genes affected by aromatic alcohol communication. In addition, through a comparative genomic analysis involving 31 fungal species, we show that the S. cerevisiaequorum sensing system is a recent evolutionary innovation and that the genes which are differentially expressed upon treatment with these molecules are distributed across the genome in a highly non-random manner. The identified transcription factors will aid in further unravelling the molecular mechanisms of S. cerevisiaequorum sensing and may facilitate the engineering of regulatory circuits for applications such as the expression of heterologous proteinsviaaromatic alcohols.

Graphical abstract: Transcriptional control of the quorum sensing response in yeast

Supplementary files

Article information

Article type
Paper
Submitted
07 Jul 2009
Accepted
10 Aug 2009
First published
01 Sep 2009

Mol. BioSyst., 2009,6, 134-141

Transcriptional control of the quorum sensing response in yeast

A. Wuster and M. M. Babu, Mol. BioSyst., 2009, 6, 134 DOI: 10.1039/B913579K

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