Antagonistic gene transcripts regulate adaptation to new growth environments

Cells have evolved complex regulatory networks that reorganize gene expression patterns in response to changing environmental conditions. These changes often involve redundant mechanisms that affect various levels of gene expression. Here, we examine the consequences of enhanced mRNA degradation in the galactose utilization network of Saccharomyces cerevisiae. We observe that glucose-induced degradation of GAL1 transcripts provides a transient growth advantage to cells upon addition of glucose. We show that the advantage arises from relief of translational competition between GAL1 transcripts and those of cyclin CLN3, a translationally regulated initiator of cell division. This competition creates a translational bottleneck that balances the production of Gal1p and Cln3p and represents a posttranscriptional control mechanism that enhances the cell's ability to adapt to changes in carbon source. We present evidence that the spatial regulation of GAL1 and CLN3 transcripts is what allows growth to be maintained during fluctuations of glucose availability. Our results provide unique insights into how cells optimize energy use during growth in a dynamic environment.

[1]  G. C. Johnston,et al.  Cell Division in the Yeast Saccharomyces cerevisiae Growing at Different Rates , 1980 .

[2]  Frederick R. Cross,et al.  Positive feedback of G1 cyclins ensures coherent cell cycle entry , 2008, Nature.

[3]  J. Monod,et al.  Genetic regulatory mechanisms in the synthesis of proteins. , 1961, Journal of Molecular Biology.

[4]  M Aldea,et al.  A Set of Vectors with a Tetracycline‐Regulatable Promoter System for Modulated Gene Expression in Saccharomyces cerevisiae , 1997, Yeast.

[5]  L. Alberghina,et al.  Control of the yeast cell cycle by protein synthesis. , 1982, Experimental cell research.

[6]  K. Bloom,et al.  ASH1 mRNA localization in three acts. , 2001, Molecular biology of the cell.

[7]  Eran Segal,et al.  Transient transcriptional responses to stress are generated by opposing effects of mRNA production and degradation , 2008, Molecular systems biology.

[8]  M. Polymenis,et al.  Coupling of cell division to cell growth by translational control of the G1 cyclin CLN3 in yeast. , 1997, Genes & development.

[9]  D. Tzamarias,et al.  A Yeast Catabolic Enzyme Controls Transcriptional Memory , 2007, Current Biology.

[10]  Mike Tyers,et al.  CDK Activity Antagonizes Whi5, an Inhibitor of G1/S Transcription in Yeast , 2004, Cell.

[11]  B. Futcher,et al.  Relationship between the function and the location of G1 cyclins in S. cerevisiae. , 2001, Journal of cell science.

[12]  Alexander van Oudenaarden,et al.  Growth Landscape Formed by Perception and Import of Glucose in Yeast , 2009, Nature.

[13]  M. Bennett,et al.  Metabolic gene regulation in a dynamically changing environment , 2008, Nature.

[14]  J Hasty,et al.  Microfluidics for synthetic biology: from design to execution. , 2011, Methods in enzymology.

[15]  David Botstein,et al.  Transcriptional response of steady-state yeast cultures to transient perturbations in carbon source. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[16]  D. Lohr,et al.  Transcriptional regulation in the yeast GAL gene family: a complex genetic network , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[17]  Curt Wittenberg,et al.  Cln3 Activates G1-Specific Transcription via Phosphorylation of the SBF Bound Repressor Whi5 , 2004, Cell.

[18]  M. Bennett,et al.  Microfluidic devices for measuring gene network dynamics in single cells , 2009, Nature Reviews Genetics.

[19]  I. Scheffler,et al.  Control of mRNA turnover as a mechanism of glucose repression in Saccharomyces cerevisiae. , 1992, The international journal of biochemistry & cell biology.

[20]  Joaquín Moreno,et al.  Genomics and gene transcription kinetics in yeast. , 2007, Trends in genetics : TIG.

[21]  I. Scheffler,et al.  The role of the 5′ untranslated region (UTR) in glucose‐dependent mRNA decay , 2002, Yeast.

[22]  K. Entian,et al.  Multiple transcripts regulate glucose-triggered mRNA decay of the lactate transporter JEN1 from Saccharomyces cerevisiae. , 2005, Biochemical and biophysical research communications.

[23]  S. Moore Kinetic evidence for a critical rate of protein synthesis in the Saccharomyces cerevisiae yeast cell cycle. , 1988, The Journal of biological chemistry.