Abstract
One central, and yet unsolved, question in evolutionary biology is the relationship between the genetic variants segregating within species and the causes of morphological differences between species. The classic neo-darwinian view postulates that species differences result from the accumulation of small-effect changes at multiple loci. However, many examples support the possible role of larger abrupt changes in the expression of developmental genes in morphological evolution1,2,3. Although this evidence might be considered a challenge to a neo-darwinian micromutationist view of evolution, there are currently few examples of the actual genes causing morphological differences between species4,5,6,7,8,9,10. Here we examine the genetic basis of a trichome pattern difference between Drosophila species, previously shown to result from the evolution of a single gene, shavenbaby (svb), probably through cis-regulatory changes6. We first identified three distinct svb enhancers from D. melanogaster driving reporter gene expression in partly overlapping patterns that together recapitulate endogenous svb expression. All three homologous enhancers from D. sechellia drive expression in modified patterns, in a direction consistent with the evolved svb expression pattern. To test the influence of these enhancers on the actual phenotypic difference, we conducted interspecific genetic mapping at a resolution sufficient to recover multiple intragenic recombinants. This functional analysis revealed that independent genetic regions upstream of svb that overlap the three identified enhancers are collectively required to generate the D. sechellia trichome pattern. Our results demonstrate that the accumulation of multiple small-effect changes at a single locus underlies the evolution of a morphological difference between species. These data support the view that alleles of large effect that distinguish species may sometimes reflect the accumulation of multiple mutations of small effect at select genes.
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Acknowledgements
We thank Y. Tao for D. mauritiana stocks and for sharing unpublished data; F. Roch for anti-Min antibody; T. Frankino for help with flies; A. Bassan, P. Valenti, Y. Latapie and S. Plaza for experimental help, discussions and critical reading of the manuscript; and W. Damen and N. Brown for hosting A.P.M. and I.D., respectively, during manuscript revisions. This work was supported by funding from the Association pour la Recherche sur le Cancer (to J.Z.), the Fondation pour la Recherche Médicale (programme équipe 2005), an EMBO Long-Term Fellowship and a BBSRC grant to I.D., a Damon Runyon Cancer Research Foundation Fellowship to V.O., a National Institute of General Medical Sciences National Research Service Award Fellowship to D.G.S., and a NIH grant and a David and Lucile Packard Foundation Fellowship to D.L.S.
Author Contributions The enhancer analysis was designed by A.P.M., I.D., F.P. and D.L.S.; DNA constructs and transgenic flies were made by A.P.M., I.D. and D.G.S.; embryos were stained, examined and photographed by A.P.M., I.D., J.Z., D.G.S., F.P. and D.L.S.; the recombination mapping experiment was designed and performed by D.L.S., V.O. and A.P.M. All authors participated in data analysis and writing of the manuscript.
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McGregor, A., Orgogozo, V., Delon, I. et al. Morphological evolution through multiple cis-regulatory mutations at a single gene. Nature 448, 587–590 (2007). https://doi.org/10.1038/nature05988
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DOI: https://doi.org/10.1038/nature05988