Citation: Mundy NI (2009) Conservation and Convergence of Colour Genetics: MC1R Mutations in brown Cavefish. PLoS Genet 5(2): e1000388. doi:10.1371/journal.pgen.1000388
Editor: Gregory S. Barsh, Stanford University School of Medicine, United States of America
Published: February 20, 2009
Copyright: © 2009 Nicholas Mundy. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The author's work on pigmentation genetics is supported by the Leverhulme Trust and Natural Environment Research Council. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The author has declared that no competing interests exist.
One of the most striking observations in nature is when similar phenotypes appear independently, such as wings in birds and bats, or melanism in moths and mice. These examples of so-called convergent evolution naturally lead us to ponder the question of genetic repeatability, i.e., the extent to which similar phenotypes that evolved in parallel share the same genetic mechanisms. Cave-dwelling organisms provide an attractive system for studying genetic repeatability, since populations in geographically isolated caves often undergo striking convergent evolution in response to the drastically altered environment, with reduced pigmentation and vision being particularly common phenotypes. In a paper recently published in PLoS Genetics , Gross et al. find that different mutations at the same locus, MC1R (Melanocortin-1 receptor), underlie the parallel evolution of reduction of pigmentation in a teleost fish, the Mexican cave tetra Astyanax mexicanus. The MC1R has been widely implicated in the evolution of colouration in birds and mammals, and the current results add to a growing body of literature showing that genetic repeatability in evolution is surprisingly common, although by no means pervasive (e.g., ). A role for MC1R in teleost pigmentation is also interesting in the light of differences in pigmentary biology between homeothermic amniotes (mammals and birds) and other vertebrates.
The authors studied the brown mutation, a recessive mutation in which A. mexicanus have paler skin and eyes than fish from surface-dwelling populations, and found that both the number of melanin-producing pigment cells (melanophores) and their melanin content were decreased in the dorsal skin. Complementation tests had previously shown that the brown mutation was probably at the same locus in several isolated caves in Northeastern Mexico, including Pachón, Yerbaniz/Japonés, Curva, and Piedras. Quantitative trait locus (QTL) mapping on an F2 derived from a surface× Pachón cave brown cross identified a single peak in logarithm of the odds (LOD) score in the genome that contained the MC1R locus based on comparative mapping to zebrafish. The authors found that brown cavefish from Pachón carried an early frameshift in MC1R (Δ24,25), whereas the brown mutation in the Yerbaniz/Japonés population carried a missense alteration, R164C—remarkably, the identical mutation at the homologous MC1R residue in humans causes a loss-of-function mutation that gives rise to red hair and fair skin . In contrast, there were no amino-acid–changing mutations in several other populations, including Curva and Piedras, suggesting that cis-regulatory mutations in MC1R may be involved in these cases. Confirmation that these MC1R mutations have functional consequences came from experiments exploiting gene knockdown technology in zebrafish. Consistent with a hypothesis of reduced or absent MC1R function in the two coding mutations, zebrafish treated with a MC1R morpholino had reduced pigmentation that could be rescued by wild-type Astyanax MC1R, but not by the Δ24,25 or R164C variants.
These results are interesting because, up until now, the sole function of MC1R in fish and other poikilotherms was considered to be short term physiological colour change to match the environment, as in frogs and chameleons . MC1R is a seven-transmembrane G-protein–coupled receptor expressed by melanophores that, when activated by the hormone MSH (melanocyte-stimulating hormone), causes intracellular dispersion of membrane-bound pigment granules (melanosomes) within the melanophore leading to darker colouration. This process is reversed in response to a second hormone, MCH (melanin-concentrating hormone) . The results from A. mexicanus show that MC1R can also function earlier in the pigmentation pathway in teleosts to affect both melanophore number and the amount of melanin in each melanophore. It will be interesting to investigate these novel functions in more detail, including how they relate to other genes involved in pigment cell development in fish .
The comparison with MC1R function in mammals and birds is instructive. In these lineages, pigment cells slowly transfer melanin granules to adjacent keratinocytes using a different set of biochemical and cell biologic pathways, and these cells are termed melanocytes to reflect this difference. Consequently, mammals and birds are unable to change their colour rapidly. Instead, a major function of MC1R in mammals and birds is to act as a switch between synthesis of dark eumelanin and phaeomelanin, a pale or reddish melanin that is apparently absent from teleosts. Thus, evolution of dark/pale colouration has involved MC1R mutations repeatedly not only in birds and mammals , (and probably also reptiles ), but now also in fish , in spite of many differences in mechanistic detail. An interesting difference, however, is that the MC1R variants in cavefish affect eye colour as well as body colour, whereas MC1R effects on eye colour have never been described in birds and mammals. More broadly, although colouration in fish (in contrast to mammals) is determined to a great extent by migration, proliferation, and cell–cell interactions among melanophores and other pigment cells , the present study adds to other reports showing a surprising amount of conservation in genes underlying melanin-based colouration among fish and mammals ,.
What do the results say about the mechanisms of evolution in cave organisms? The evolutionary forces acting on loss-of-function phenotypes such as brown are hotly debated. Potential explanations for the rise in frequency of such phenotypes fall chiefly into three categories: (i) purely neutral, i.e., arising from genetic drift and/or inbreeding; (ii) direct selection for the loss-of-function phenotype, e.g., because of energetic constraints; and (iii) indirect selection on the loss-of-function phenotype arising as a correlated response to selection on a second trait controlled either by pleiotropic action of the same locus or by a closely linked locus. Assessing the relative importance of these mechanisms for brown is made complex but more intriguing by the presence of a second and more dramatic colour phenotype—albinism—which the same lab has shown to be caused by independent mutations in the OCA2 locus . Albinism masks (i.e., is epistatic to) the expression of brown, and wild populations contain differing proportions of albino and brown individuals. The Yerbaniz/Japonés population is fixed for albinism, so it could be that the brown mutation it contains (the R164C variant) has never been expressed, in which case neutral causes would be most likely. In contrast, the Pachón population has a mixture of both phenotypes. The most one can speculate here is that because MC1R and OCA2 are unlinked, it would be surprising if the third mechanism was acting on both loci. From this perspective, it would be interesting to perform population genetic studies in this system to determine the relative importance of genetic drift and selection in loss of colouration and investigate the relative ages of the mutations at the different loci.
- 1. Gross JB, Borowsky R, Tabin CJ (2009) A novel role for Mc1r in the parallel evolution of depigmentation in independent populations of the cavefish Astyanax mexicanus. PLoS Genet 5(1): e1000326. doi:10.1371/journal.pgen.1000326.
- 2. Gompel N, Prud'homme B, Wittkopp PJ, Kassner VA, Carroll SB (2005) Chance caught on the wing: cis-regulatory evolution and the origin of pigment patterns in Drosophila. Nature 433: 481–487.
- 3. Valverde P, Healy E, Jackson I, Rees JL, Thody AJ (1995) Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nat Genet 11: 328–330.
- 4. Bagnara JT (1998) Comparative anatomy and physiology of pigment cells in nonmammalian tissues. In: Nordlund JJ, Boissy RE, Hearing VJ, King RA, Oetting WS, et al., editors. The pigmentary system - physiology and pathophysiology. New York: Oxford University Press. pp. 9–40.
- 5. Kelsh RN (2004) Genetics and evolution of pigment patterns in fish. Pigment Cell Res 17: 326–336.
- 6. Hoekstra HE, Hirschmann RJ, Bundey RA, Insel PA, Crossland JP (2006) A single amino acid mutation contributes to adaptive beach mouse color pattern. Science 313: 101–104.
- 7. Mundy NI, Badcock NS, Hart T, Scribner K, Janssen K, et al. (2004) Conserved genetic basis of a quantitative plumage trait involved in mate choice. Science 303: 1870–1873.
- 8. Rosenblum EB, Hoekstra HE, Nachman MW (2004) Adaptive reptile color variation and the evolution of the Mc1r gene. Evolution 58: 1794–1808.
- 9. Parichy DM (2003) Pigment patterns: fish in stripes and spots. Curr Biol 13: R947–950.
- 10. Miller CT, Beleza S, Pollen AA, Schluter D, Kittles RA, et al. (2007) cis-regulatory changes in Kit ligand expression and parallel evolution of pigmentaiton in sticklebacks and humans. Cell 131: 1179–1189.
- 11. Lamason RL, Mohideen MA, Mest JR, Wong AC, Norton HL, et al. (2005) SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310: 1782–1786.
- 12. Protas ME, Hersey C, Kochanek D, Zhou Y, Wilkens H, et al. (2006) Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism. Nat Genet 38: 107–111.