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 [1], 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., [2]). 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 [3]. 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 [4]. 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) [4]. 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 [5].
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 [6],[7] (and
probably also reptiles [8]), but now also in fish [1], 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 [9], the present
study adds to other reports showing a surprising amount of conservation in genes underlying
melanin-based colouration among fish and mammals [10],[11].
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 [12]. 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.