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Genomic Diversity and Evolution of the Head Crest in the Rock Pigeon

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Science  01 Mar 2013:
Vol. 339, Issue 6123, pp. 1063-1067
DOI: 10.1126/science.1230422

Coo Coo

Charles Darwin was fascinated by the domestic rock pigeon and used this dramatic example of diversity within a species to communicate his ideas about natural selection. Many derived traits in domestic pigeons converge on ecologically and evolutionarily relevant traits in wild species. Shapiro et al. (p. 1063, published online 31 January; see the cover) sequenced the genome of the domestic rock pigeon (Columba livia), along with those of 36 breeds and two feral accessions and its sister species, the hill pigeon (C. rupestris). The results reveal the underlying genetics of the head crest and suggest that all crested breeds may have originated from a single mutational event.

Abstract

The geographic origins of breeds and the genetic basis of variation within the widely distributed and phenotypically diverse domestic rock pigeon (Columba livia) remain largely unknown. We generated a rock pigeon reference genome and additional genome sequences representing domestic and feral populations. We found evidence for the origins of major breed groups in the Middle East and contributions from a racing breed to North American feral populations. We identified the gene EphB2 as a strong candidate for the derived head crest phenotype shared by numerous breeds, an important trait in mate selection in many avian species. We also found evidence that this trait evolved just once and spread throughout the species, and that the crest originates early in development by the localized molecular reversal of feather bud polarity.

Since the initial domestication of the rock pigeon in Neolithic times (1), breeders have selected striking differences in behavior, vocalizations, skeletal morphology, feather ornaments, colors, and color patterns to establish over 350 breeds (2). In many cases, the number and magnitude of differences among breeds are more characteristic of macroevolutionary changes than of changes within a single species (2, 3). Indeed, Charles Darwin was so fascinated by domestic pigeons that he repeatedly called attention to this dramatic example of diversity within a species to communicate his ideas about natural selection (3, 4).

The genetic architecture for many derived traits in pigeons is probably relatively simple (5, 6), probably more so than that for interspecific trait variation among many wild species, because breeders often focus on qualitative rather than quantitative variation; this increases the chance of identifying genes responsible for differences among breeds. Additionally, several morphological traits show similar patterns of variation in different breeds, making it possible to test whether the same or different genes underlie similar phenotypes. Despite these advantages, the pigeon is underused as a model for the molecular genetic basis of avian variation because of the paucity of genetic and genomic resources for this bird.

We examined genomic diversity, genetic structure, and phylogenetic relationships among domestic breeds and feral populations (free-living birds descended from escaped domestics) of the rock pigeon. The pigeon reference genome was sequenced from a male Danish tumbler with the Illumina HiSeq 2000 platform, and we also resequenced 40 additional Columba livia genomes to 8- to 26-fold coverage (38 individuals from 36 domestic breeds and two feral pigeons) (7). Genome-wide nucleotide diversity in the rock pigeon (π = 3.6 × 10−3) and the mutation rate estimate in the pigeon lineage (1.42 × 10−9 substitutions per site per year ± 2.60 × 10−12 SE) are comparable to those of other avian species (8, 9). The observed heterozygosity indicates a large effective population size for the rock pigeon of Ne ≈ 521,000; demographic inferences based on the allele frequency spectrum indicate that, aside from a very recent bottleneck, Ne has been remarkably stable over the past 1.5 million generations (7).

Patterns of linkage disequilibrium (LD) are indicative of haplotype sizes and genome-wide recombination rates and inform decisions about genetic mapping strategies. Using genotype data from the 40 resequenced C. livia genomes, we found that mean "useful LD" (10) (coefficient of determination, r2 > 0.3) decays in 2.2 kb (fig. S10J). This suggests that we should expect little LD between typical pairs of genes in an analysis across breeds; thus, the pigeon is well suited for association-mapping strategies.

We leveraged our whole-genome data to determine breed relationships, using 1.48 million variable loci. A neighbor-joining tree rooted on C. rupestris, the sister species of C. livia (11), yielded several well-supported groups (Fig. 1 and fig. S16). Notably, the two feral pigeons grouped with the wattle and homer breeds (Fig. 1, pink branches), supporting the idea that escaped racing homers are probably major contributors to feral populations (12). As with many domesticated species, pigeon evolution is probably not exclusively linear or hierarchical (12). We therefore examined genetic structure among breeds by analyzing 3950 loci with ADMIXTURE (13) and found a best model fit at K = 1 (a single population, where K is the number of assumed ancestral populations). However, higher values of K can also be biologically informative (figs. S17 to S20). Our analysis includes some of the oldest lineages of domestic pigeons and breeds that were not exported from the Middle East until the late 19th or early 20th centuries (14), providing information about likely geographic origins of breeds and their exchange along ancient trade routes (7).

Fig. 1

Relationships among rock pigeons and the hill pigeon C. rupestris. A consensus neighbor-joining tree based on 1.48 million genomic SNPs and 1000 bootstrap replicates (see fig. S16 for bootstrap support) is shown. Branches are colored according to traditional breed groups (12) and/or geographic affinities: orange, toy breeds; brown, pouters and utility breeds; light blue, Indian and Iranian breeds; green, tumblers and highflyers; pink, homers and wattle breeds; red, Mediterranean and owl breeds; black, voice characteristics (14). Bold red lettering indicates breeds with the head crest phenotype. Scale bar, Euclidean distance. [Photo credits: T. Hellmann (domestic breeds) and M. V. Shreeram (C. rupestris)]

Derived traits in domesticated birds tend to evolve along a predictable temporal trajectory, with color variation appearing in the earliest stages of domestication, followed by plumage and structural (skeletal and soft tissue) variation, and finally behavioral differences (2). One of the genetically simplest derived traits of pigeons is the head crest. Head crests are common ornaments in many bird species (2) and are important display structures in mate selection (15). In pigeons, head crests consist of neck and occipital feathers with reversed growth polarity, so that the feathers grow toward the top of the head instead of down the neck. Crests can be as small and simple as a peak of feathers or as elaborate as the hood of the Jacobin, which envelops the head (Fig. 2A). Classical genetics experiments suggest that the head crest segregates as a simple Mendelian recessive trait (6, 14). Moreover, previous studies suggest that the same locus controls the presence of a crest in numerous breeds, either with alternative alleles at this locus or additional modifier loci controlling the extent of crest development (6, 14).

Fig. 2

EphB2 is associated with the derived head crest phenotype. (A) Head crests are variable among breeds (left to right: Indian fantail, Old German owl, Old Dutch capuchin, Jacobin). (B) FST between crested and uncrested pigeons, with maximum value for individual SNPs plotted for nonoverlapping 100-kb windows across the genome. Red star, window with the highest score. Dashed red line, top 1% of scores. (C) Genome-wide VAAST scan. Each dot represents a single gene. Red star, gene with the highest score. Dashed red line, genome-wide significance cutoff. (D) Magnification of scaffold 612 in shaded region of (B) and (C). Black trace, maximum FST between crested and uncrested birds over a 300-SNP window. Red trace, unstandardized cross-population extended haplotype homozygosity (XP-EHH); higher values are evidence of selection (see fig. S21, genome-wide plot). Dashed vertical line, position of the lone genome-wide significant VAAST hit. Green bar, the 27.4-kb haplotype shared by all crested birds, includes only the EphB2 gene. Blue bars, gene predictions on + and – DNA strands. (E) The cr mutation induces a charge-changing amino acid substitution; black bar, highly conserved DLAARN motif of catalytic loop. (F) Genotypes of 159 birds from 79 breeds at the cr locus are perfectly associated with the crest phenotype under a recessive model. (G) Network diagram of the minimal 11-kb haplotype shared by all resequenced rock pigeons with the cr mutation (also see fig. S23). Many haplotypes contain the + allele (blue), but only one contains the cr SNP (red). The sizes of the circles are proportional to the number of chromosomes containing a haplotype. Line segments represent single-nucleotide differences. [Jacobin photo credit: T. Hellmann]

We resequenced eight individuals with head crests to directly test whether the same mutation controls crest development in different breeds. We sorted genomic variants from birds with and without head crests into separate bins and calculated allele frequency differentiation (FST) across the genome (Fig. 2B). We identified a region of high differentiation between crested and uncrested birds in the pigeon ortholog of Ephrin receptor B2 (EphB2; FST = 0.94, top hit genome-wide; fig. S22A) (Fig. 2D). The role of EphB2 in feather growth is not known, but it plays important roles in tissue patterning and morphogenesis and is a member of a receptor tyrosine kinase family that mediates development of the feather cytoskeleton (16, 17). All eight crested birds were homozygous for a T nucleotide at scaffold 612, position 596613 (hereafter, the cr allele), whereas uncrested birds were heterozygous (n = 3) or homozygous (n = 30, including the uncrested outgroup C. rupestris) for the putatively ancestral C nucleotide (the + allele). These results were consistent with the known simple recessive architecture of the trait and implicated a common polymorphism associated with head crest development in multiple breeds with different genetic histories (Fig. 1). This trend extended well beyond our resequencing panel: We genotyped an additional 61 crested birds from 22 breeds and 69 uncrested birds from 57 breeds, and found a perfect association between cr/cr genotype and the crest phenotype (Fig. 2F). By treating the genomes of crested and uncrested birds as separate populations, we also found suggestive evidence for positive selection around the cr allele using cross-population extended haplotype homozygosity analysis (Fig. 2D and figs. S21 and S22B).

We then used the Variant Annotation, Analysis, and Search Tool [VAAST (18)] to investigate the pigeon genomes for additional coding changes associated with the head crest phenotype. This identified one gene with genome-wide significance: EphB2, and specifically the cr single-nucleotide polymorphism (SNP) (Pgenome = 2.0 × 10−8) (Fig. 2, C and D). The cr allele has a predicted charge-changing arginine (basic) to cysteine (polar uncharged) transition in the catalytic loop of the intracellular tyrosine kinase domain of EphB2 (Fig. 2E). This amino acid position is invariant among other vertebrates, suggesting strong purifying selection for conserved protein function. The same DLAARN to DLAACN motif change we observe in EphB2 is sufficient to abrogate kinase activity in human and mouse orthologs of the protein tyrosine kinase ZAP-70, and in both mammals and pigeons the mutant phenotypes are inherited recessively (19). Hence, the pigeon cr mutation probably abrogates kinase activity in EphB2 and disrupts downstream signal propagation, consistent with the high VAAST score for this gene. EphB2 is therefore a convincing candidate for the cr locus of classical pigeon genetics (57, 14).

In several wild and domesticated species, the repeated evolution of a derived trait has occurred by selection on the same gene, possibly owing to the repeated selection on the same allele or haplotype (2022). Similarly, the cr SNP is part of a 27.4-kb haplotype that is shared by all crested pigeons, suggesting that the mutation occurred just once and spread to multiple breeds by introgression among domestic breeds, or was selected repeatedly from a standing variant in wild rock pigeons (Fig. 2G and fig. S23; the core haplotype containing the cr mutation is reduced to 11 kb when uncrested heterozygotes are included). The only gene present in the shared cr haplotype is EphB2 (Fig. 2D, green bar), although at this time we cannot rule out the presence of regulatory variants that might alter the expression of another gene. Crested members of the toy, fantail, Iranian, Jacobin, and owl breed groups are not more closely related to each other than to uncrested breeds (Fig. 1). Nevertheless, members of these groups had head crests hundreds of years ago (14), so some of these introgression events must have occurred in the distant past. Breeds with a wide variety of crest phenotypes share the same derived allele; therefore, allelic variation at the cr locus alone does not control all aspects of crest development (14). Other genetic and developmental factors beyond this locus must contribute to variation in crest morphology, akin to the presumed complex genetic architecture of species-level divergence in feather ornaments (2).

In crested pigeons, feather placode polarity and bud outgrowth are inverted during embryogenesis (Fig. 3). Expression of EphB2 is not polarized in early placodes (fig. S26), so the effects of the cr mutation on feather polarity are probably exerted earlier in development. Why might the crest phenotype be limited to the head and neck? In Naked neck chicken mutants, regionalized production of retinoic acid allows uniform up-regulation of Bmp7 expression to change skin phenotypes in the neck but not the body (23). Similarly, the head crests of several chicken breeds, in which feathers are elongated but do not have a reversed growth trajectory as in pigeons, are localized to the top of the head, probably due to ectopic expression of Hox positional cues (24). Together these examples provide evidence for regionalization of the developing head and neck skin in the chicken. We propose that analogous mechanisms might underlie skin regionalization in the pigeon and allow cr to change feather polarity in the occiput and neck, but not elsewhere.

Fig. 3

Feather bud polarity is reversed in the cr mutant. (A and B) Expression of the feather structural gene Ctnnb1 reveals the direction of outgrowth of early feather buds. St., Hamburger-Hamilton embryonic stage. (A) Neck and occipital head expression of Ctnnb1 in an embryo of the uncrested racing homer. Feather buds point downward along the contour of the head and neck (arrowheads). (B) Occipital feather buds point upward in the equivalent region of the crested English trumpeter, indicating morphological reversal of feather orientation. (C and D) Expression of the polarity marker EphA4 was assayed at an earlier developmental stage to test whether feather placodes, the ectodermal thickenings that give rise to feather buds, are also reversed. (C) Polarity marker EphA4 is expressed posteriorly (arrowheads) in feather placodes of the racing homer. (D) The polarity of placodes is reversed in the English trumpeter. Expression of EphB2 in the skin is weak and unpolarized at this stage in both morphs (fig. S26).

Our study of domestic rock pigeons illustrates how combining comparative genomics and population-based analyses forwards our understanding of genetic relationships and the genomic basis of traits. Many of the traits that vary among pigeon breeds also vary among wild species of birds and other animals (2, 25); thus, pigeons are a model for identifying the genetic basis of variation in traits of general interest. Moreover, variation in many traits in domestic pigeons, including the head crest phenotype described here, is constructive rather than regressive: Breeds derived from the ancestral rock pigeon possess traits that the ancestor does not have. Although adaptive regressive traits are important, the genetic basis of constructive traits in vertebrates remains comparatively poorly understood. The domestic pigeon is thus a promising model with which to explore the genetic architecture of derived, constructive phenotypes in a bird that is amenable to genetic, genomic, and developmental investigation.

Supplementary Materials

www.sciencemag.org/cgi/content/full/science.1230422/DC1

Materials and Methods

Supplementary Text

Figs. S1 to S27

Tables S1 to S28

References (2672)

References and Notes

  1. See the supplementary materials on Science Online.
  2. Acknowledgments: We thank the University of Washington Burke Museum for the C. rupestris tissue sample (UWBM 59803); J. Oldham, K. Wright, the Utah Pigeon Club, the National Pigeon Association, and A. and H. O. Christiansen for domestic pigeon samples; D. Clayton for feral samples; and D. Clayton, M. Horvath, D. Kingsley, R. Nielsen, and W. Warren for discussion and comments. Supported by a Burroughs Wellcome Fund Career Award in the Biomedical Sciences, NSF CAREER DEB-1149160, University of Utah Research Foundation (M.D.S.); NIH training grant T32GM007464 (S.A.S.); NIH training grant T32HD07491 (E.T.D.); an NSF EDEN internship (A.I.V.); NIH/NHGRI R01HG004694 and NIH ARRA GO RC2HG005619 (M.Y.); and the Danish National Research Foundation (M.T.P.G. and E.W.). We acknowledge a computer time allocation from the Center for High Performance Computing at the University of Utah. This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under accession no. AKCR00000000 (the first version described here is AKCR01000000; raw reads, SRA052637); RNA-seq data for annotation, accession no. GSE39333; and raw reads for resequenced genomes, accession no. SRA054391.
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