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:

Role of duplicate genes in genetic robustness against null mutations

Abstract

Deleting a gene in an organism often has little phenotypic effect1,2,3,4,5, owing to two mechanisms of compensation4,5,6,7,8,9,10. The first is the existence of duplicate genes: that is, the loss of function in one copy can be compensated by the other copy or copies. The second mechanism of compensation stems from alternative metabolic pathways, regulatory networks, and so on. The relative importance of the two mechanisms has not been investigated except for a limited study, which suggested that the role of duplicate genes in compensation is negligible10. The availability of fitness data for a nearly complete set of single-gene-deletion mutants of the Saccharomyces cerevisiae genome11 has enabled us to carry out a genome-wide evaluation of the role of duplicate genes in genetic robustness against null mutations. Here we show that there is a significantly higher probability of functional compensation for a duplicate gene than for a singleton, a high correlation between the frequency of compensation and the sequence similarity of two duplicates, and a higher probability of a severe fitness effect when the duplicate copy that is more highly expressed is deleted. We estimate that in S. cerevisiae at least a quarter of those gene deletions that have no phenotype are compensated by duplicate genes.

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: Distributions of fitness (f).
Figure 2: Distribution of mean fitness differences between randomly selected gene pairs (100,000 replicates each with 418 gene pairs) under the YPD growth condition.
Figure 3: Relationship between protein distance and fitness effect of deletion.

Similar content being viewed by others

References

  1. Winzeler, E. A. et al. Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis. Science 285, 901–906 (1999)

    Article  CAS  Google Scholar 

  2. Cadigan, K. M., Grossniklaus, U. & Gehring, W. J. Functional redundancy: the respective roles of the 2 sloppy paired genes in Drosophila segmentation. Proc. Natl Acad. Sci. USA 91, 6324–6328 (1994)

    Article  ADS  CAS  Google Scholar 

  3. Saga, Y., Yagi, T., Ikawa, Y., Sakakura, T. & Aizawa, S. Mice develop normally without tenascin. Genes Dev. 6, 1821–1831 (1992)

    Article  CAS  Google Scholar 

  4. Gibson, T. J. & Spring, J. Genetic redundancy in vertebrates: polyploidy and persistence of genes encoding multidomain proteins. Trends Genet. 14, 46–49 (1998)

    Article  CAS  Google Scholar 

  5. Normanly, J. & Bartel, B. Redundancy as a way of life—IAA metabolism. Curr. Opin. Plant Biol. 2, 207–213 (1999)

    Article  CAS  Google Scholar 

  6. Brookfield, J. F. Y. Can genes be truly redundant? Curr. Biol. 2, 553–554 (1992)

    Article  CAS  Google Scholar 

  7. Nowak, M. A., Boerlijst, M. C., Cooke, J. & Smith, J. M. Evolution of genetic redundancy. Nature 388, 167–171 (1997)

    Article  ADS  CAS  Google Scholar 

  8. Tautz, D. Redundancies, development and the flow of information. BioEssays 14, 263–266 (1992)

    Article  CAS  Google Scholar 

  9. Maslov, S. & Sneppen, K. Specificity and stability in topology of protein networks. Science 296, 910–913 (2002)

    Article  ADS  CAS  Google Scholar 

  10. Wagner, A. Robustness against mutations in genetic networks of yeast. Nature Genet. 24, 355–361 (2000)

    Article  CAS  Google Scholar 

  11. Steinmetz, L. M. et al. Systematic screen for human disease genes in yeast. Nature Genet. 31, 400–404 (2002)

    Article  CAS  Google Scholar 

  12. Seoighe, C. & Wolfe, K. H. Yeast genome evolution in the post-genome era. Curr. Opin. Microbiol. 2, 548–554 (1999)

    Article  CAS  Google Scholar 

  13. Lynch, M. & Conery, J. S. The evolutionary fate and consequences of duplicate genes. Science 290, 1151–1155 (2000)

    Article  ADS  CAS  Google Scholar 

  14. Conant, G. C. & Wagner, A. GenomeHistory: a software tool and its application to fully sequenced genomes. Nucleic Acids Res. 30, 3378–3386 (2002)

    Article  CAS  Google Scholar 

  15. Ohno, S. Evolution by Gene Duplication (Springer, Berlin, 1970)

    Book  Google Scholar 

  16. 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 

  17. Pearson, W. R. & Lipman, D. J. Improved tools for biological sequence analysis. Proc. Natl Acad. Sci. USA 85, 2444–2448 (1988)

    Article  ADS  CAS  Google Scholar 

  18. Kitami, T. & Nadeau, J. H. Biochemical networking contributes more to genetic buffering in human and mouse metabolic pathways than does gene duplication. Nature Genet. 32, 191–194 (2002)

    Article  CAS  Google Scholar 

  19. Giaever, G. et al. Functional profiling of the Saccharomyces cerevisiae genome. Nature 418, 387–391 (2002)

    Article  ADS  CAS  Google Scholar 

  20. Gu, Z., Cavalcanti, A., Chen, F.-C., Bouman, P. & Li, W.-H. Extent of gene duplication in the genomes of Drosophila, nematode, and yeast. Mol. Biol. Evol. 19, 256–262 (2002)

    Article  CAS  Google Scholar 

  21. Thompson, J. D., Higgins, D. G. & Gibson, T. J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22, 4673–4680 (1994)

    Article  CAS  Google Scholar 

  22. Yang, Z. & Nielsen, R. Estimating synonymous and nonsynonymous substitution rates under realistic evolutionary models. Mol. Biol. Evol. 17, 32–43 (2000)

    Article  CAS  Google Scholar 

  23. Holstege, F. C. P. et al. Dissecting the regulatory circuitry of a eukaryotic genome. Cell 95, 717–728 (1998)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank M. Long, T. Oakley, D. Nicolae, K. Thornton, A. Deutschbauer and J. Zhang for discussions and comments. This work was supported by NIH grants to W.H.L and to R.W.D.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Wen-Hsiung Li.

Ethics declarations

Competing interests

The authors declare that they have no competing financial interests.

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gu, Z., Steinmetz, L., Gu, X. et al. Role of duplicate genes in genetic robustness against null mutations. Nature 421, 63–66 (2003). https://doi.org/10.1038/nature01198

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature01198

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