Gene duplication and the evolution of ribosomal protein gene regulation in yeast

Coexpression of genes within a functional module can be conserved at great evolutionary distances, whereas the associated regulatory mechanisms can substantially diverge. For example, ribosomal protein (RP) genes are tightly coexpressed in Saccharomyces cerevisiae, but the cis and trans factors asso...

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Main Authors: Regev, Aviv (Contributor), Wapinski, Ilan (Author), Pfiffner, Jenna (Author), French, Courtney (Author), Socha, Amanda (Author), Thompson, Dawn Anne (Author)
Other Authors: Massachusetts Institute of Technology. Department of Biology (Contributor)
Format: Article
Language:English
Published: National Academy of Sciences (U.S.), 2011-03-01T23:06:11Z.
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Online Access:Get fulltext
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100 1 0 |a Regev, Aviv  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Biology  |e contributor 
100 1 0 |a Regev, Aviv  |e contributor 
100 1 0 |a Regev, Aviv  |e contributor 
700 1 0 |a Wapinski, Ilan  |e author 
700 1 0 |a Pfiffner, Jenna  |e author 
700 1 0 |a French, Courtney  |e author 
700 1 0 |a Socha, Amanda  |e author 
700 1 0 |a Thompson, Dawn Anne  |e author 
245 0 0 |a Gene duplication and the evolution of ribosomal protein gene regulation in yeast 
260 |b National Academy of Sciences (U.S.),   |c 2011-03-01T23:06:11Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/61365 
520 |a Coexpression of genes within a functional module can be conserved at great evolutionary distances, whereas the associated regulatory mechanisms can substantially diverge. For example, ribosomal protein (RP) genes are tightly coexpressed in Saccharomyces cerevisiae, but the cis and trans factors associated with them are surprisingly diverged across Ascomycota fungi. Little is known, however, about the functional impact of such changes on actual expression levels or about the selective pressures that affect them. Here, we address this question in the context of the evolution of the regulation of RP gene expression by using a comparative genomics approach together with cross-species functional assays. We show that an activator (Ifh1) and a repressor (Crf1) that control RP gene regulation in normal and stress conditions in S. cerevisiae are derived from the duplication and subsequent specialization of a single ancestral protein. We provide evidence that this regulatory innovation coincides with the duplication of RP genes in a whole-genome duplication (WGD) event and may have been important for tighter control of higher levels of RP transcripts. We find that subsequent loss of the derived repressor led to the loss of a stress-dependent repression of RPs in the fungal pathogen Candida glabrata. Our comparative computational and experimental approach shows how gene duplication can constrain and drive regulatory evolution and provides a general strategy for reconstructing the evolutionary trajectory of gene regulation across species. 
520 |a Alfred P. Sloan Foundation 
520 |a Howard Hughes Medical Institute 
520 |a Burroughs Wellcome Fund 
520 |a National Institutes of Health (U.S.) 
520 |a Broad Institute of MIT and Harvard 
520 |a Human Frontier Science Program (Strasbourg, France) 
546 |a en_US 
655 7 |a Article 
773 |t Proceedings of the National Academy of Sciences of the United States of America. (PNAS)