An incoherent feedforward loop facilitates adaptive tuning of gene expression

Author:

Hong Jungeui12,Brandt Nathan1,Abdul-Rahman Farah1,Yang Ally3,Hughes Tim3,Gresham David1ORCID

Affiliation:

1. Department of Biology, Center for Genomics and Systems Biology, New York University, New York, United States

2. Memorial Sloan Kettering Cancer Center, New York, United States

3. Banting and Best Department of Medical Research, Donnelly Centre, University of Toronto, Toronto, Canada

Abstract

We studied adaptive evolution of gene expression using long-term experimental evolution of Saccharomyces cerevisiae in ammonium-limited chemostats. We found repeated selection for non-synonymous variation in the DNA binding domain of the transcriptional activator, GAT1, which functions with the repressor, DAL80 in an incoherent type-1 feedforward loop (I1-FFL) to control expression of the high affinity ammonium transporter gene, MEP2. Missense mutations in the DNA binding domain of GAT1 reduce its binding to the GATAA consensus sequence. However, we show experimentally, and using mathematical modeling, that decreases in GAT1 binding result in increased expression of MEP2 as a consequence of properties of I1-FFLs. Our results show that I1-FFLs, one of the most commonly occurring network motifs in transcriptional networks, can facilitate adaptive tuning of gene expression through modulation of transcription factor binding affinities. Our findings highlight the importance of gene regulatory architectures in the evolution of gene expression.

Funder

National Science Foundation

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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