Article

Nature 449, 54-61 (6 September 2007) | doi:10.1038/nature06107; Received 21 March 2007; Accepted 20 July 2007

Natural history and evolutionary principles of gene duplication in fungi

Ilan Wapinski1,2,3, Avi Pfeffer3, Nir Friedman4 & Aviv Regev1,5

  1. Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA
  2. FAS Center for Systems Biology, Harvard University, 7 Divinity Avenue
  3. School of Engineering and Applied Sciences, Harvard University, 33 Oxford Street, Cambridge, Massachusetts 02138, USA
  4. School of Computer Science and Engineering, Hebrew University, Jerusalem 91904, Israel
  5. Department of Biology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA

Correspondence to: Aviv Regev1,5 Correspondence and requests for materials should be addressed to A.R. (Email: aregev@broad.mit.edu).

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Gene duplication and loss is a powerful source of functional innovation. However, the general principles that govern this process are still largely unknown. With the growing number of sequenced genomes, it is now possible to examine these events in a comprehensive and unbiased manner. Here, we develop a procedure that resolves the evolutionary history of all genes in a large group of species. We apply our procedure to seventeen fungal genomes to create a genome-wide catalogue of gene trees that determine precise orthology and paralogy relations across these species. We show that gene duplication and loss is highly constrained by the functional properties and interacting partners of genes. In particular, stress-related genes exhibit many duplications and losses, whereas growth-related genes show selection against such changes. Whole-genome duplication circumvents this constraint and relaxes the dichotomy, resulting in an expanded functional scope of gene duplication. By characterizing the functional fate of duplicate genes we show that duplicated genes rarely diverge with respect to biochemical function, but typically diverge with respect to regulatory control. Surprisingly, paralogous modules of genes rarely arise, even after whole-genome duplication. Rather, gene duplication may drive the modularization of functional networks through specialization, thereby disentangling cellular systems.

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