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Birth of a metabolic gene cluster in yeast by adaptive gene relocation

Abstract

Although most eukaryotic genomes lack operons, they contain some physical clusters of genes that are related in function despite being unrelated in sequence1,2,3,4,5. How these clusters are formed during evolution is unknown. The DAL cluster is the largest metabolic gene cluster in yeast and consists of six adjacent genes encoding proteins that enable Saccharomyces cerevisiae to use allantoin as a nitrogen source6. We show here that the DAL cluster was assembled, quite recently in evolutionary terms, through a set of genomic rearrangements that happened almost simultaneously. Six of the eight genes involved in allantoin degradation, which were previously scattered around the genome, became relocated to a single subtelomeric site in an ancestor of S. cerevisiae and Saccharomyces castellii. These genomic rearrangements coincided with a biochemical reorganization of the purine degradation pathway, which switched to importing allantoin instead of urate. This change eliminated urate oxidase, one of several oxygen-consuming enzymes that were lost by yeasts that can grow vigorously in anaerobic conditions. The DAL cluster is located in a domain of modified chromatin involving both H2A.Z histone exchange and Hst1-Sum1–mediated histone deacetylation, and it may be a coadapted gene complex formed by epistatic selection.

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Figure 1: The allantoin degradation pathway.
Figure 2: Conservation and disruption of the DAL gene cluster.
Figure 3: Locations of the DAL genes in K. waltii as compared with S. cerevisiae.

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References

  1. Hurst, L.D., Pal, C. & Lercher, M.J. The evolutionary dynamics of eukaryotic gene order. Nat. Rev. Genet. 5, 299–310 (2004).

    Article  CAS  Google Scholar 

  2. Qi, X. et al. A gene cluster for secondary metabolism in oat: implications for the evolution of metabolic diversity in plants. Proc. Natl. Acad. Sci. USA 101, 8233–8238 (2004).

    Article  CAS  Google Scholar 

  3. Lee, J.M. & Sonnhammer, E.L. Genomic gene clustering analysis of pathways in eukaryotes. Genome Res. 13, 875–882 (2003).

    Article  CAS  Google Scholar 

  4. Keller, N.P. & Hohn, T.M. Metabolic pathway gene clusters in filamentous fungi. Fungal Genet. Biol. 21, 17–29 (1997).

    Article  CAS  Google Scholar 

  5. Blumenthal, T. & Gleason, K.S. Caenorhabditis elegans operons: form and function. Nat. Rev. Genet. 4, 112–120 (2003).

    Article  CAS  Google Scholar 

  6. Cooper, T.G. Regulation of allantoin catabolism in Saccharomyces cerevisiae . in The Mycota III: Biochemistry and Molecular Biology (ed. Marzluf, G.A.) 139–169 (Springer, Berlin, 1996).

    Chapter  Google Scholar 

  7. Pal, C. & Hurst, L.D. Evidence for co-evolution of gene order and recombination rate. Nat. Genet. 33, 392–395 (2003).

    Article  CAS  Google Scholar 

  8. Cohen, B.A., Mitra, R.D., Hughes, J.D. & Church, G.M. A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression. Nat. Genet. 26, 183–186 (2000).

    Article  CAS  Google Scholar 

  9. Hurst, L.D., Williams, E.J. & Pal, C. Natural selection promotes the conservation of linkage of co-expressed genes. Trends Genet. 18, 604–606 (2002).

    Article  CAS  Google Scholar 

  10. Hittinger, C.T., Rokas, A. & Carroll, S.B. Parallel inactivation of multiple GAL pathway genes and ecological diversification in yeasts. Proc. Natl. Acad. Sci. USA 101, 14144–14149 (2004).

    Article  CAS  Google Scholar 

  11. Kellis, M., Birren, B.W. & Lander, E.S. Proof and evolutionary analysis of ancient genome duplication in the yeast Saccharomyces cerevisiae . Nature 428, 617–624 (2004).

    Article  CAS  Google Scholar 

  12. Kurtzman, C.P. & Robnett, C.J. Phylogenetic relationships among yeasts of the 'Saccharomyces complex' determined from multigene sequence analyses. FEMS Yeast Res. 3, 417–432 (2003).

    Article  CAS  Google Scholar 

  13. Hartig, A. et al. Differentially regulated malate synthase genes participate in carbon and nitrogen metabolism of S. cerevisiae . Nucleic Acids Res. 20, 5677–5686 (1992).

    Article  CAS  Google Scholar 

  14. LaRue, T.A. & Spencer, J.F. The utilization of purines and pyrimidines by yeasts. Can. J. Microbiol. 14, 79–86 (1968).

    Article  CAS  Google Scholar 

  15. van der Klei, I.J. & Veenhuis, M. Yeast peroxisomes: function and biogenesis of a versatile cell organelle. Trends Microbiol. 5, 502–509 (1997).

    Article  CAS  Google Scholar 

  16. Piskur, J. & Langkjaer, R.B. Yeast genome sequencing: the power of comparative genomics. Mol. Microbiol. 53, 381–389 (2004).

    Article  CAS  Google Scholar 

  17. Deak, T. & Beuchat, L.R. Handbook of Food Spoilage Yeasts (CRC Press, Boca Raton, Florida, USA, 1996).

    Google Scholar 

  18. Kwast, K.E. et al. Genomic analyses of anaerobically induced genes in Saccharomyces cerevisiae: functional roles of Rox1 and other factors in mediating the anoxic response. J. Bacteriol. 184, 250–265 (2002).

    Article  CAS  Google Scholar 

  19. Peoples, M.B. & Gifford, R.M. Regulation of the transport of nitrogen and carbon in higher plants. in Plant Metabolism (eds. Dennis, D.T., Layzell, D.B., Lefebvre, D.D. & Turpin, D.H.) 525–538 (Longman, Singapore, 1997).

    Google Scholar 

  20. Bursell, E. The excretion of nitrogen in insects. Adv. Insect Physiol. 4, 33–67 (1967).

    Article  CAS  Google Scholar 

  21. Nei, M. Modification of linkage intensity by natural selection. Genetics 57, 625–641 (1967).

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Robyr, D. et al. Microarray deacetylation maps determine genome-wide functions for yeast histone deacetylases. Cell 109, 437–446 (2002).

    Article  CAS  Google Scholar 

  23. Meneghini, M.D., Wu, M. & Madhani, H.D. Conserved histone variant H2A.Z protects euchromatin from the ectopic spread of silent heterochromatin. Cell 112, 725–736 (2003).

    Article  CAS  Google Scholar 

  24. Krogan, N.J. et al. A Snf2 family ATPase complex required for recruitment of the histone H2A variant Htz1. Mol. Cell 12, 1565–1576 (2003).

    Article  CAS  Google Scholar 

  25. Robert, F. et al. Global position and recruitment of HATs and HDACs in the yeast genome. Mol. Cell 16, 199–209 (2004).

    Article  CAS  Google Scholar 

  26. Pierce, M. et al. Sum1 and Ndt80 proteins compete for binding to middle sporulation element sequences that control meiotic gene expression. Mol. Cell. Biol. 23, 4814–4825 (2003).

    Article  CAS  Google Scholar 

  27. Kellis, M., Patterson, N., Endrizzi, M., Birren, B. & Lander, E.S. Sequencing and comparison of yeast species to identify genes and regulatory elements. Nature 423, 241–254 (2003).

    Article  CAS  Google Scholar 

  28. Daran-Lapujade, P. et al. Comparative genotyping of the Saccharomyces cerevisiae laboratory strains S288C and CEN.PK113–7D using oligonucleotide microarrays. FEMS Yeast Res. 4, 259–269 (2003).

    Article  CAS  Google Scholar 

  29. Gerton, J.L. et al. Global mapping of meiotic recombination hotspots and coldspots in the yeast Saccharomyces cerevisiae . Proc. Natl. Acad. Sci. USA 97, 11383–11390 (2000).

    Article  CAS  Google Scholar 

  30. Takada, Y. & Tsukiji, N. Peroxisomal localization and activation by bivalent metal ions of ureidoglycolate lyase, the enzyme involved in urate degradation in Candida tropicalis . J. Bacteriol. 169, 2284–2286 (1987).

    Article  CAS  Google Scholar 

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Acknowledgements

We thank D. Scannell, K. Byrne, J. Gordon, G. Conant, N. Khaldi, B. Cusack, L. Rusche, J. Conery and anonymous referees for comments. This study was supported by Science Foundation Ireland.

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Correspondence to Kenneth H Wolfe.

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The authors declare no competing financial interests.

Supplementary information

Supplementary Fig. 1

Organization of the DAL clusters of S. cerevisiae aned S. castellii. (PDF 84 kb)

Supplementary Fig. 2

Locations of DALgenes (red) in species lacking the DAL cluster. (PDF 421 kb)

Supplementary Fig. 3

Phylogenetic trees of Dal4/Fur4 and Dal7/Mls1 sequences. (PDF 40 kb)

Supplementary Fig. 4

The DAL cluster is a meiotic recombination coldspot. (PDF 30 kb)

Supplementary Table 1

Sequence evolution in DAL genes. (PDF 68 kb)

Supplementary Note (PDF 48 kb)

Supplementary Methods (PDF 55 kb)

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Wong, S., Wolfe, K. Birth of a metabolic gene cluster in yeast by adaptive gene relocation. Nat Genet 37, 777–782 (2005). https://doi.org/10.1038/ng1584

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