Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Growth-regulated recruitment of the essential yeast ribosomal protein gene activator Ifh1

Abstract

Regulation of ribosome biogenesis is central to the control of cell growth1. In rapidly growing yeast cells, ribosomal protein (RP) genes account for approximately one-half of all polymerase II transcription-initiation events1, yet these genes are markedly and coordinately downregulated in response to a number of environmental stress conditions2,3,4, or during the transition from fermentation to respiration5. Although several conserved signalling pathways (TOR, RAS/protein kinase A and protein kinase C) impinge upon RP gene transcription1, little is known about how initiation at these genes is controlled. Rap1 (refs 6, 7) and more recently Fhl1 (ref. 8) were shown to bind upstream of many RP genes. Here we show that the essential protein Ifh1 binds to and activates many RP gene promoters under optimal growth conditions in Saccharomyces cerevisiae. Ifh1 is recruited to RP gene promoters through the forkhead-associated domain of Fhl1. Ifh1 binding decreases when RP genes are downregulated either by TOR inhibition or nutrient depletion, and is restored after release from starvation or upon regulated induction of IFH1 expression. These findings indicate a central role for Ifh1 and Fhl1 in RP gene regulation.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Ifh1, Fhl1 and Rap1 binding at RP gene (RPG) promoters, and mRNA levels during logarithmic growth, before the diauxic shift or after TOR inhibition.
Figure 2: Rapamycin-sensitive recruitment of Ifh1 to an ectopic site (GAL7) via the FHA domain of GBD–Fhl1 hybrids.
Figure 3: Ifh1 directly activates RP gene transcription.

Similar content being viewed by others

References

  1. Warner, J. R. The economics of ribosome biosynthesis in yeast. Trends Biochem. Sci. 24, 437–440 (1999)

    Article  CAS  Google Scholar 

  2. Gasch, A. P. et al. Genomic expression programs in the response of yeast cells to environmental changes. Mol. Biol. Cell 11, 4241–4257 (2000)

    Article  CAS  Google Scholar 

  3. Causton, H. C. et al. Remodeling of yeast genome expression in response to environmental changes. Mol. Biol. Cell 12, 323–337 (2001)

    Article  CAS  Google Scholar 

  4. Rep, M., Krantz, M., Thevelein, J. M. & Hohmann, S. The transcriptional response of Saccharomyces cerevisiae to osmotic shock. Hot1p and Msn2p/Msn4p are required for the induction of subsets of high osmolarity glycerol pathway-dependent genes. J. Biol. Chem. 275, 8290–8300 (2000)

    Article  CAS  Google Scholar 

  5. Ju, Q. & Warner, J. R. Ribosome synthesis during the growth cycle of Saccharomyces cerevisiae. Yeast 10, 151–157 (1994)

    Article  CAS  Google Scholar 

  6. Lieb, J. D., Liu, X., Botstein, D. & Brown, P. O. Promoter-specific binding of Rap1 revealed by genome-wide maps of protein-DNA association. Nature Genet. 28, 327–334 (2001)

    Article  CAS  Google Scholar 

  7. Shore, D. RAP1: a protean regulator in yeast. Trends Genet. 10, 408–412 (1994)

    Article  CAS  Google Scholar 

  8. Lee, T. I. et al. Transcriptional regulatory networks in Saccharomyces cerevisiae. Science 298, 799–804 (2002)

    Article  ADS  CAS  Google Scholar 

  9. Hermann-Le Denmat, S., Werner, M., Sentenac, A. & Thuriaux, P. Suppression of yeast RNA polymerase III mutations by FHL1, a gene coding for a fork head protein involved in rRNA processing. Mol. Cell. Biol. 14, 2905–2913 (1994)

    Article  CAS  Google Scholar 

  10. Cherel, I. & Thuriaux, P. The IFH1 gene product interacts with a fork head protein in Saccharomyces cerevisiae. Yeast 11, 261–270 (1995)

    Article  CAS  Google Scholar 

  11. DeRisi, J. L., Iyer, V. R. & Brown, P. O. Exploring the metabolic and genetic control of gene expression on a genomic scale. Science 278, 680–686 (1997)

    Article  ADS  CAS  Google Scholar 

  12. Jacinto, E. & Hall, M. N. Tor signalling in bugs, brain and brawn. Nature Rev. Mol. Cell Biol. 4, 117–126 (2003)

    Article  CAS  Google Scholar 

  13. Cardenas, M. E., Cutler, N. S., Lorenz, M. C., Di Como, C. J. & Heitman, J. The TOR signaling cascade regulates gene expression in response to nutrients. Genes Dev. 13, 3271–3279 (1999)

    Article  CAS  Google Scholar 

  14. Hardwick, J. S., Kuruvilla, F. G., Tong, J. K., Shamji, A. F. & Schreiber, S. L. Rapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins. Proc. Natl Acad. Sci. USA 96, 14866–14870 (1999)

    Article  ADS  CAS  Google Scholar 

  15. Powers, T. & Walter, P. Regulation of ribosome biogenesis by the rapamycin-sensitive TOR-signaling pathway in Saccharomyces cerevisiae. Mol. Biol. Cell 10, 987–1000 (1999)

    Article  CAS  Google Scholar 

  16. Ren, B. et al. Genome-wide location and function of DNA binding proteins. Science 290, 2306–2309 (2000)

    Article  ADS  CAS  Google Scholar 

  17. Harismendy, O. et al. Genome-wide location of yeast RNA polymerase III transcription machinery. EMBO J. 22, 4738–4747 (2003)

    Article  CAS  Google Scholar 

  18. Koranda, M., Schleiffer, A., Endler, L. & Ammerer, G. Forkhead-like transcription factors recruit Ndd1 to the chromatin of G2/M-specific promoters. Nature 406, 94–98 (2000)

    Article  ADS  CAS  Google Scholar 

  19. Jorgensen, P. & Tyers, M. The fork'ed path to mitosis. Genome Biol. 1, R1022.1–1022.4 (2000)

    Article  Google Scholar 

  20. Durocher, D. & Jackson, S. P. The FHA domain. FEBS Lett. 513, 58–66 (2002)

    Article  CAS  Google Scholar 

  21. Klein, C. & Struhl, K. Protein kinase A mediates growth-regulated expression of yeast ribosomal protein genes by modulating RAP1 transcriptional activity. Mol. Cell. Biol. 14, 1920–1928 (1994)

    Article  CAS  Google Scholar 

  22. Mencia, M., Moqtaderi, Z., Geisberg, J. V., Kuras, L. & Struhl, K. Activator-specific recruitment of TFIID and regulation of ribosomal protein genes in yeast. Mol. Cell 9, 823–833 (2002)

    Article  CAS  Google Scholar 

  23. Reid, J. L., Iyer, V. R., Brown, P. O. & Struhl, K. Coordinate regulation of yeast ribosomal protein genes is associated with targeted recruitment of Esa1 histone acetylase. Mol. Cell 6, 1297–1307 (2000)

    Article  CAS  Google Scholar 

  24. Rohde, J. R. & Cardenas, M. E. The tor pathway regulates gene expression by linking nutrient sensing to histone acetylation. Mol. Cell. Biol. 23, 629–635 (2003)

    Article  CAS  Google Scholar 

  25. Jorgensen, P., Nishikawa, J. L., Breitkreutz, B. J. & Tyers, M. Systematic identification of pathways that couple cell growth and division in yeast. Science 297, 395–400 (2002)

    Article  ADS  CAS  Google Scholar 

  26. Marion, R. M. et al. Sfp1 is a stress- and nutrient-sensitive regulator of ribosomal protein gene expression. Proc. Natl Acad. Sci. USA 101, 14315–14322 (2004)

    Article  ADS  CAS  Google Scholar 

  27. Jorgensen, P. et al. A dynamic transcriptional network communicates growth potential to ribosome synthesis and critical cell size. Genes Dev. 18, 2491–2505 (2004)

    Article  CAS  Google Scholar 

  28. Kim, M., Ahn, J. W., Song, K., Paek, K. H. & Pai, H. S. Forkhead-associated domains of the tobacco NtFHA1 transcription activator and the yeast Fhl1 forkhead transcription factor are functionally conserved. J. Biol. Chem. 277, 38781–38790 (2002)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank J. Warner, E. Di Mauro, K. Mizuta, G. Ammerer, P. Thuriaux and M. Tyers for discussions; J. Warner, K. Struhl and M. Tyers for communicating unpublished results; A. Bianchi for comments on the manuscript; members of the Shore laboratory for discussions; P. Descombes, C. Barraclough, C. Delucinge, O. Schaad, P. Soularue and X. Gidrol for help with microarray experiments and analysis; S. Gasser for providing antibodies; and N. Roggli for artwork. This work was supported by the Human Frontier Science Program, the Swiss National Science Foundation, the NCCR program ‘Frontiers in Genetics’ (Swiss National Science Foundation), and the Canton of Geneva.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to David Shore.

Ethics declarations

Competing interests

The authors declare that they have no competing financial interests.

Supplementary information

Supplementary Methods (DOC 66 kb)

Supplementary Table 1

Fhl1-myc and Ifh1-myc binding to intergenic regions in cells untreated, or treated for 90 min with rapamycin. For each experiment, we generated a list of enriched intergenic regions (according to the criteria described in Supplementary Information, Methods) that was sorted according to p-value. For each enriched locus, we indicated the intergenic region identifier, the median log enrichment ratio, the p-value, the ORF(s) under the control of this promoter region on both strands (if applicable) and the Gene Ontology (GO; if applicable) of individual genes except RP genes. (HTM 233 kb)

Supplementary Figure 1

a, Ifh1-myc, Fhl1-myc, and Rap1 protein levels during diauxic shift, rapamycin treatment and re-growth from stationary phase. b, Ifh1-myc binding at RP gene promoters is restored immediately after release from starvation (see Supplementary Information, Methods). (PDF 229 kb)

Supplementary Figure 2

Genome-wide binding of Fhl1-myc and Ifh1-myc to intergenic regions and global (genome-wide) association of Fhl1-myc and Ifh1-myc with RP gene promoters, as measured in the absence of rapamycin and 90 min following rapamycin treatment. (PDF 215 kb)

Supplementary Figure 3

Ifh1 directly activates RP gene transcription. This Figure is a reproduction of Fig. 3a in which individual gene names can be read. (PDF 199 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schawalder, S., Kabani, M., Howald, I. et al. Growth-regulated recruitment of the essential yeast ribosomal protein gene activator Ifh1. Nature 432, 1058–1061 (2004). https://doi.org/10.1038/nature03200

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature03200

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing