The guppy (Poecilia reticulata) is an important model organism for studying sexual selection; male guppies have complex and conspicuous pigmentation, and female guppies exhibit preferences for males with specific color spots. Understanding the genetic basis underlying pigmentation variation in the guppy is important for exploring the factors causing the maintenance of color polymorphism in wild populations.
Findings We focused on the melanic black pigmentation of guppies, and examined genetic variations in the melanocortin 1 receptor (MC1R) gene because variation in this gene is known to contribute to polymorphism of melanin pigmentation in several animal species. The complete coding sequence of the guppy MC1R gene was determined, and two different MC1R alleles (963 and 969 bp) were found in wild populations. Ornamental strain guppies with a 963-bp MC1R tended to show less black pigmentation than those with a 969-bp MC1R, although the association between MC1R genotype and black pigmentation disappeared in the F2 offspring.
Conclusions The guppy MC1R gene showed variation in the five wild Trinidadian populations we examined, and these populations also differed in terms of allele frequencies. We identified a significant association between black pigmentation and MC1R genotype in fish obtained from aquarium shops. However, the results from F2 families suggest that there are other genes that modify the effects of the MC1R gene.
Background Pigmentation plays important roles in various aspects of several animal species, including camouflage, warning, thermoregulation, protection from ultraviolet radiation, and courtship display [1]. Therefore, individual variation in pigmentation can be a target of both natural and sexual selection, and thus mutations that change pigmentation influence adaptive evolution. Recently, identification of the genes responsible for pigmentation polymorphism has gained considerable attention in evolutionary biology [2]. The guppy (Poecilia reticulata) exhibits extreme pigmentation polymorphism in the secondary sexual traits of males, which is complex, conspicuous, and manifested as spots, speckles, and lines of various pigmented colors, including black, white, red-orange, yellow and green [3]. These fish also display iridescent structural color [3]. Female guppies show preferences for a specific type of male pigmentation, including orange and black, and various color spots [3]. Although directional selection such as specific female preference is expected to reduce variation in male traits [4], various color spots are maintained as polymorphic traits within populations [3]. Many studies have attempted to explain the maintenance of body color variation in the guppy and have suggested that maintenance of male pigmentation polymorphism is caused by negative frequency-dependent selection [5,6], selection maintaining multiple traits within populations [7], and/or gene flow with divergent selection [8]. Although several evolutionary mechanisms have been proposed, none has been conclusively demonstrated. One of the obstacles to elucidating the evolutionary mechanisms is the lack of information on the genetic basis of pigmentation, since the evolutionary responses to selection for the pigmentation depend largely on how the phenotypes are controlled by genes. For example, the selection force for coloration will be influenced according to whether the genes involved in melanogenesis show multiple pleiotropic effects [9]. Male guppies display many types of color pigment on their bodies. In this study, we particularly focused on a candidate gene that contributes to the polymorphism of black pigmentation. Black pigmentation in guppies plays two distinct roles, namely, in nuptial display and in camouflage. Females from populations with a higher proportion of orange coloration tend to have a stronger preference for orange and black [10]. In contrast, natural selection is predicted to operate against conspicuous black spots in habitats with visually hunting predatory fish (i.e., the so-called "high-predation sites") [11]. Black pigmentation is produced by melanin synthesis, which involves many genes. The coding sequence of one of these genes, melanocortin 1 receptor (MC1R), is reported to contain variations that are associated with melanin pigmentation polymorphism in natural populations in many animals [Reviewed in 2]. Among the pigmentation genes, MC1R plays a crucial role in controlling melanin synthesis [12]. In mammals and birds, high activity of MC1R leads to the synthesis of black eumelanin, whereas low activity leads to reddish pheomelanin, or an absence of melanin synthesis [13,14]. In contrast, fish melanophores contain only eumelanin and are unable to produce pheomelanin [15]. Thus, in guppies, like other fishes, lower activity of MC1R may lead to an absence of black pigmentation. In this study, we focused on MC1R as a candidate gene that contributes to the polymorphism of black pigmentation in guppies. The purpose of this study was to determine the complete coding sequence of guppy MC1R, and to examine whether MC1R polymorphisms are present in wild guppy populations in contrasting habitats. We also examined whether sequence variation in MC1R affect black pigmentation by comparing MC1R genotypes and body color phenotypes.
Results DNA sequencing of guppy MC1R and MC1R polymorphism
We determined the complete coding sequence and partial untranslated regions of the guppy MC1R gene. The complete coding sequence of the guppy MC1R gene contains 969 bp (+), which is predicted to encode a protein of 322 amino acids. The 969-bp guppy MC1R gene has the same length as the MC1R gene of a related species, the platyfish Xiphophorus maculatus (GenBank accession number DQ866828) [21]. To examine whether MC1R polymorphism is present in wild populations, we genotyped 270 individuals sampled from five wild populations in Trinidad. MC1R polymorphism was observed in two of these wild populations: Pitch Lake and Lower Guanapo River (Table 2). We identified two alleles of the guppy MC1R gene differing in length by 6 bp: one allele of 969 bp (+) (GenBank number AB563501); the other of 963 bp (Del) (GenBank number AB563502), which lacks two amino acids (Ser35 and Ser36) in the extracellular region. We determined the sequences using four indel-flanking primers. When we compared the sequences of homo- and heterozygous individuals, we found those from the heterozygotes to be unreadable. We were unable to detect any further alleles in any of the homozygotes examined in this study. Figure 3 shows an amino acid alignment of the extracellular region and the transmembrane region of MC1R that includes the deleted sites. We designated the homozygous genotype of the 963-bp (Del) length morph "Del/Del" and that of the 969-bp (+) length morph "+/+." In the Pitch Lake population, genotype frequencies were in approximate Hardy-Weinberg equilibrium (Table 2). A small non-significant deviation in the +/Del genotype was observed in the Lower Guanapo population (Ho = 0.040 and He = 0.113) (randomization test: p = 0.163).
Figure 3. Amino acid alignment in the extracellular region and the transmembrane region surrounding the deletion sites in MC1R. The sites of the deletion mutation in guppy MC1R are highlighted. Dashes and cross marks indicate sequence identities and insertion/deletion differences, respectively. These sequences are as follows: Platyfish X. maculatus (DQ866828), Tilapia Oreochromis mossambicus (AJ871147), Stickleback Gasterosteus aculeatus (group II contig 348), Tetraodon Tetraodon nigroviridis (AY332238), Medaka Oryzias latipes (scaffold 45), Zebrafish Danio rerio (NM_180970), Chicken Gallus gallus (NM_001031462), Human Homo sapiens (AF326275), and Mouse Mus musculus (NM_008559).
Individuals with the 963-bp (Del) allele were mostly found in Pitch Lake. There was a significant difference in the frequency of the 963-bp (Del) allele among the five wild populations sampled (G = 48.243, df = 4, P < 0.0001). The frequencies of the 963-bp (Del) allele in Pitch Lake (PL) and the Lower Guanapo River (LG) were significantly higher than those in the other three populations (a simultaneous test procedure using the G-test: PL vs. LG, G = 4.822, df = 4, P = 0.306; PL and LG vs. Upper Aripo River, G = 20.1681, df = 4, P < 0.0004).
[bearbeiten]Association between MC1R genotypes and black pigmentation We examined the association between the genotypes of MC1R (+/+, +/Del, and Del/Del) and black pigmentation using the specimens obtained from aquarium shops. The typical black pigmentation of each MC1R genotype is shown in Figure 2. In males, +/+ individuals tended to exhibit a grayish body color and have black traits, whereas the +/Del and Del/Del individuals tended to exhibit a yellowish body color and have no black traits, which suggests that the yellowish pigmentation was highly visible in these individuals because black pigmentation was absent. In females, the +/+ individuals tended to exhibit a grayish body color, whereas the Del/Del individuals tended to exhibit a yellowish color. The +/Del females had phenotypes intermediate between those of +/+ and Del/Del. We found statistically significant differences in the frequencies of different genotypes (+/+:Del/Del, +/+:+/Del, and +/+:+/Del:Del/Del) between different body blackness (Grayish vs. Yellowish) and also in the frequencies of different genotypes (+/+:Del/Del, and +/+:+/Del:Del/Del) between different black traits (Black vs. None) (Table 3) (sequential Bonferroni corrections after Fisher's exact test: P < 0.05).
Association between MC1R genotypes and black pigmentation in F1 and F2 We obtained two F2 families (N = 39) from eight F1 individuals established by crossing two different homozygotes. The composition ratio of genotypes in the F2 individuals deviated from 1:2:1, with the +/Del genotype occurring at a frequency slightly greater than expected (overall ratio: 8:24:7). However, this bias was statistically non-significant (Fisher's exact test: P = 0.2) All of the F1 individuals had grayish body color and black traits. The association between genotype and black pigmentation in the F2 individuals is shown in Table 4. There was no significant association between MC1R genotype and body blackness (Grayish vs. Yellowish) or between MC1R genotype and black trait (Black vs. None) (Fisher's exact test: P > 0.05) (Table 4).
Discussion This study showed that there was MC1R polymorphism both within and among wild guppy populations. We identified two alleles of the MCIR gene that differed in length by 6 bp: 969 bp (+) and 963 bp (Del). The 969-bp (+) guppy MC1R gene is the same length as the MC1R gene of the platyfish, which is a related species. Thus, the 963-bp (Del) guppy MC1R allele may have lost a 6-bp sequence after divergence between the guppy and the platyfish. Although several studies have reported that polymorphism of color-related genes is maintained in wild fish populations [22-24], this is the first study to detect polymorphism in the color-related genes of guppies in the wild. The present study showed that the frequency of the 963-bp (Del) allele of MC1R was higher in the Pitch Lake population than in the other sampled populations. Unlike guppies in the other populations, those in Pitch Lake are exposed to direct sunlight and high water temperatures, and the background color of the sediment in this habitat is black [25]. Similarly, a uniquely colored killifish (Rivulus hartii) with pink and white hue and two mottled darker patches has been reported in the Pitch Lake [26]. The relatively abundant lighter colored fish with +/Del and Del/Del genotypes may therefore be particularly conspicuous in the Pitch Lake environment. MC1R polymorphisms are associated with coloration in approximately half of the investigated species [9,27-35]. These authors mostly suggest that MC1R polymorphism contributes to the adaptation to divergent background colorations for crypsis. For example, in pocket mice (Chaetodipus intermedius), melanic MC1R mutants are found on dark lava fields, whereas light-colored mutants are found on light-colored rocks, suggesting that these variations in MC1R contribute to adaptive camouflage for predator avoidance on different backgrounds [28-30]. On the other hand, in several bird species, it has been reported that MC1R polymorphism is selected by sexual selection [31]. For example, in arctic skuas, females prefer dark males, and also those males having the same color as that of their parents, which contributes to positive assortative mating [32]. At this stage of our study, it is unclear whether the differences in allele frequencies across populations have been caused by random genetic drift and natural selection. To test the hypothesis that the differences are a result of natural or sexual selection, we ideally need to use statistical methods for detecting natural selection. The present results suggest that there is a significant association between MC1R genotype and black pigmentation in the guppies obtained from aquarium shops (Table 3). These results indicate that the deletion of two amino acids in MCIR disturbed both overall grayish body blackness and black traits. MC1R plays crucial roles in controlling melanin synthesis [12]; therefore, by mutating MC1R, it is possible to increase or decrease melanin synthesis. Thus, deletion of two amino acids in the extracellular regions (Figure 3) might affect the affinity of MC1R for its ligands, i.e., MSH and β-defensin. If the affinity for these ligands is decreased, melanin synthesis is disturbed. In this study, most of the Del/Del individuals exhibited less distinct black pigmentation than +/+ individuals, and thus the deletion of two amino acids in MC1R might inhibit black pigment production. However, three of 14 Del/Del individuals had black pigmentation (Table 3), suggesting that other factors are involved in pigmentation. Furthermore, no association between MC1R genotype and black pigmentation could be found in the investigation using F2 individuals (Table 4). However, in this case, it is possible that, owing to an excess of heterozygous (+/Del) individuals, there was an insufficient number of homozygous F2 offspring to enable detection of an association. There are two possible explanations to account for the lack of association between genotypes and phenotypes in the F2 population. First, the variously pigmented guppies found in aquarium fish shops are created by selective breeding. Thus, we cannot fully exclude the possibility that ancestral founders of the strains with white body color had a deletion allele of MC1R that did not affect black pigmentation. However, we used several different strains with white body color, and thus it is seems unlikely that the founders of these different strains simultaneously had a 963-bp (Del) allele of MC1R. Second, the existence of certain other modifier genes may have an effect on black pigmentation. Epistasis may alter the predicted association between genotype and phenotype. For example, in the pathway of melanin synthesis, MC1R activation and inhibition is influenced by melanocortin (e.g. ACTH, MSH, and β-defensin) and ASIP [9]. It is possible that these genes can modify the effects of the MC1R gene on melanin synthesis. In beach mice and flycatchers, pigmentation polymorphism in some populations can be explained by MC1R genotypes; however, in other populations, pigmentation polymorphism cannot be explained by the MC1R genotype, even though these populations exhibit similar pigmentation [33-35]. In addition, in this study, we were only able to obtain F2 individuals from two pairs (two crosses of Del/Del males and +/+ females), and thus there is a possibility that paternal or maternal genotypes affected the relationship between MC1R genotype and black pigmentation. In guppies, melanism may be controlled by multiple genes, which might be the genetic basis for the complex black pigmentation patterns in these fish. Further genetic studies are needed to confirm the relationships between MC1R genotypes and black pigmentation using established commercial strains and wild guppy populations. In the present study, we identified two alleles of the MCIR gene that differ in length, namely, a 969-bp (+) and a 963-bp (Del) allele. MC1R polymorphism is present in wild populations, and we found that allele frequencies were significantly different among the different populations examined. Guppies with a 963-bp (Del) MC1R tend to exhibit less black pigmentation than those with a 969-bp (+) MC1R. Although the results of this study indicate the possibility of an association between MC1R genotype and black pigmentation, results from the study of F2 individuals did not allow us to confirm the link between MC1R genotype and black pigmentation. This suggests that there are other genes that modify the effects of the MC1R gene.
GCD
GGD
DGLZ
DGD
DGF
IGPD
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IGMX
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