The genetics of ray pattern variation in Caenorhabditis briggsae
© Baird et al; licensee BioMed Central Ltd. 2005
Received: 20 October 2004
Accepted: 05 January 2005
Published: 05 January 2005
How does intraspecific variation relate to macroevolutionary change in morphology? This question can be addressed in species in which derived characters are present but not fixed. In rhabditid nematodes, the arrangement of the nine bilateral pairs of peripheral sense organs (rays) in tails of males is often the most highly divergent character between species. The development of ray pattern involves inputs from hometic gene expression patterns, TGFβ signalling, Wnt signalling, and other genetic pathways. In Caenorhabditis briggsae, strain-specific variation in ray pattern has provided an entrée into the evolution of ray pattern. Some strains were fixed for a derived pattern. Other strains were more plastic and exhibited derived and ancestral patterns at equal frequencies.
Recombinant inbred lines (RILs) constructed from crosses between the variant C. briggsae AF16 and HK104 strains exhibited a wide range of phenotypes including some that were more extreme than either parental strain. Transgressive segregation was significantly associated with allelic variation in the C. briggsae homolog of abdominal B, Cb-egl-5. At least two genes that affected different elements of ray pattern, ray position and ray fusion, were linked to a second gene, mip-1. Consistent with this, the segregation of ray position and ray fusion phenotypes were only partially correlated in the RILs.
The evolution of ray pattern has involved allelic variation at multiple loci. Some of these loci impact the specification of ray identities and simultaneously affect multiple ray pattern elements. Others impact individual characters and are not constrained by covariance with other ray pattern elements. Among the genetic pathways that may be involved in ray pattern evolution is specification of anteroposterior positional information by homeotic genes.
A fundamental problem of morphological evolution is how does microevolution relate to macroevolution . Are variation and selection within species sufficient to account for genetic divergence between species? One approach to this problem has been comparative developmental genetic studies in closely related species. This approach is complicated by developmental redundancy and cryptic variation [2–4]. Developmental redundancy occurs in species pairs in which similar adult morphologies are attained through distinct developmental processes. For example, in the nematodes Caenorhabditis elegans and Oscheius tipulae, cells in the vulval equivalence group that do not participate in vulval development are eliminated through fusion with the multinucleated syncytial epidermis [5–8]. In Pristionchus pacificus, that same outcome is achieved through apoptosis . Cryptic variation occurs in species pairs in which the same developmental process is regulated through divergent genetic mechanisms. For example, Drosophila melanogaster and D. simulans have similar numbers and patterns of bristles. Hybrids have fewer bristles than either parental species [10, 11]. Thus, the conserved bristle phenotypes of D. melanogaster and D. simulans mask cryptic variation in the genetic regulation of bristle pattern.
Another approach has been the study of morphological variation within species. In the butterfly Bicyclus anynana, expression patterns of distalless (dll), engrailed (en), and spalt (sal) coincide with eyespot coloration patterns [12, 13]. Moreover, allelic variation in distalless has been associated with size variation in eyespots . Thus, evolution of eyespot patterns may have resulted from selection for variant alleles of dll, en, and sal. Consistent with this model, conservation of the expression patterns of these genes in developing eyespots has been demonstrated in multiple butterfly species . Developmental variation also has been characterized in several nematode species. For example, variant patterns of cell division in the ventral epidermis have been described in C. elegans, C. briggsae, and O. tipulae .
Another promising model for microevolutionary studies of morphological evolution is ray pattern variation in rhabditid nematodes. The rays are male-specific peripheral sense organs that mediate mating behavior [15–17]. In most rhabditid species there are nine bilateral pairs of rays embedded within the copulatory bursa of the tail . The pattern of rays; their anteroposterior placement and the dorsoventral position of their sensory endings, generally are constant within species but often are the most divergent character between species . Ray pattern in adult males is determined by cell contacts that form between ray structural cells and the surrounding cells of the lateral epidermis in L4 larvae [19, 20]. These contacts in turn are determined by the specification of 'ray identities' . In Caenorhabditis elegans, ray identities are specified through the integration of several regulatory inputs including: positional information from homeotic genes [22–26]; TGF-beta-like signalling [27–29]; Wnt signalling ; and ephrin/semaphorin signalling .
The ray pattern of Caenorhabditis briggsae differs from that of C. elegans in the placement of ray 3 [31, 32]. In C. elegans males, ray 3 is located at the cloaca and is separate from from all other rays. In the canonical C. briggsae ray pattern, ray 3 is located in a posterior cluster of rays 3–6 and frequently is fused with ray 4. The C. elegans ray pattern is shared with several other Caenorhabditis species and is ancestral to the Elegans-group , a monophyletic clade that includes C. briggsae [34–36]. The C. briggsae ray pattern is mimicked by several C. elegans mutations including mutations in homeotic genes or in genes that regulate homeotic gene expression patterns [21, 22, 26, 37, 38]. Thus, the derived C. briggsae ray pattern may have arisen through changes in the specification of anteroposterior positional identities. It now is possible to address this hypothesis as variant C. briggsae strains that express an ancestral ray pattern at high frequencies have been identified . In this paper, the segregation of ray pattern phenotypes in crosses between C. briggsae strains is described.
The elements of ray pattern
The derived ray pattern of C. briggsae entails the posterior displacement of ray 3 from a position level with the cloaca to the post-cloacal cluster of rays 4 – 6 and the frequent fusion of ray 3 with ray 4 [31, 32, 34]. This ray pattern is exhibited in nearly all males of C. briggsae strains AF16 and VT847 . Ray pattern in C. briggsae strains HK104, HK105, and PB800 is more variable. These strains exhibit the derived and ancestral ray patterns at approximately equal frequencies .
Segregation of C. briggsae ray pattern phenotypes
Several RILs exhibited ancestral or derived phenotypes at frequencies more extreme than either parental strain (Figure 2a). This was true for both the position of ray 3 and for fusions of rays 3 and 4. For ray 3 position, one quarter of the RILs exhibited phenotypes more extreme than either parental strain. For ray fusions, half of the RILs were more extreme than the parental strains. Such transgressive segregation is best explained through the presence, in both AF16 and HK104, of alleles at some loci that promoted ancestral character states and alleles at other loci that promoted derived character states. The high frequency of RILs with extreme phenotypes indicated that both parental strains likely were fixed for antagonistic alleles at multiple loci.
A relatively strong correlation was observed between variation in the position of ray 3 and its fusion with ray 4 (r = 0.797; Figure 2a). This correlation was highly significant (p = 2.5 × 10-23). This was expected as rays 3 and 4 could not have fused unless they were adjacent to each other  and because the placement of rays and fusion between rays have been considered to be pleiotropic phenotypes derivative of the specification of ray identities [19, 22–25, 27–30]. If anything, it was surprising that the correlation was not stronger. Based on the observed correlation coefficient, approximately one third of the variation in ray fusion frequency was independent of variation in the position of ray 3. This was readily apparent when the frequency distributions of these two ray pattern elements were compared (Figure 2b). The frequency distribution for the placement of ray 3 was highly skewed toward the derived phenotype. The frequency distribution for fusions of rays 3 and 4 was much broader and was only slightly skewed. The differences in the shapes of these distributions were significant (Kolmgorov-Smirnov, D = 0.4396, p < 0.001).
Neither the frequency distribution for the placement of ray 3 nor that for the fusion of ray3 to ray 4 were normal (p = 0.00 and p = 0.03, respectively; Figure 2b). The frequency distribution for the placement of ray 3 was highly skewed toward the derived phenotype. This result was inconsistent with the placement of ray 3 being governed strictly by additive affects. More likely, the placement of ray 3 was regulated by epistasis. Twentynine per cent of RILs exhibited the most extreme phenotype (Figure 2b). Fixation of derived alleles at as few as two major-effect genes could have been sufficient to ensure a posterior localization of ray 3 at this frequency. The frequency distribution for fusions of rays 3 and 4 was very broad and and only slightly skewed. This was consistent with ray fusion being a complex character with inputs from multiple developmental processes. At least one of these processes was shared with ray positioning; rays 3 and 4 could not have fused if they were not adjacent.
Association of ray pattern with allelic variation in homeotic genes
Cosegregation of Cb-egl-5 with ray pattern phenotypes.
6.2 × 10-4
4.2 × 10-5
mip-1 marker-assisted introgression
The segregation of phenotypes in the RILs indicated that multiple major-effect and additive loci were involved in ray pattern variation in C. briggsae. Because a high density recombination map for C. briggsae has not yet been constructed, it is not possible to identify these loci through QTL analyses. However, a limited number of mutations with visible phenotypes have been mapped to C. briggsae chromosomes [B. Gupta, pers. comm., ]. These mutations all were generated in an AF16 background. One such mutation defines the gene mip-1. mip-1 very likely is the C. briggsae homolog of C. elegans unc-22 [D. Baillie, pers. comm.]. In C. elegans, unc-22 is located on chromosome IV and is linked to several genes known to regulate homeotic gene expression patterns, e.g. lin-49 which encodes a bromodomain protein thought to be involved in chromatin remodeling . mip-1 marker-assisted introgression was used to determine if any genes linked to it were involved in ray pattern variation in C. briggsae.
Comparison of mip-1 introgressed lines.
p values for reciprocal chi-squared tests1
9.6 × 10-30
3.3 × 10-54
6.5 × 10-32
5.3 × 10-46
7.9 × 10-4
1.2 × 10-5
2.2 × 10-7
2.8 × 10-6
2.3 × 10-9
1.3 × 10-4
6.9 × 10-4
1.5 × 10-5
3.6 × 10-4
3.2 × 10-4
1.32 × 10-29
6.4 × 10-53
8.3 × 10-30
1.65 × 10-36
5.3 × 10-3
3.1 × 10-3
9.8 × 10-6
3.1 × 10-5
4.74 × 10-6
9.37 × 10-7
1.33 × 10-16
1.59 × 10-6
Ray pattern in C. briggsae varies with respect to the placement of ray 3 and fusions of ray 3 to ray 4. Ancestral states for these characters in the Elegans-group of Caenorhabditis are an anterior location, level with the cloaca, and the absence of ray fusions . Derived states are a posterior location, clustered with rays 4 through 6, and fusion of rays 3 and 4. An unexpected result was the incomplete correlation between the position or ray 3 and its fusion with ray 4. In C. elegans, mutations that alter ray position have been accompanied by ray fusion. For this reason, ray position and ray fusion were thought to be pleiotropic phenotypes that arose from the specification of ray identities [19, 22–25, 30]. Because of this, it was expected that ray pattern evolution would involve changes in suites of covariant characters rather than independent modification of individual ray pattern elements. However, only two-thirds of variation in ray fusion resulted from variation in ray position (r2 = 0.635). Moreover, evidence for a gene affecting only ray fusion was obtained from comparisons of ray patterns exhibited by the mip-1 introgressed strains. Hence, variation in ray pattern evolution is not wholey constrained by the specification of ray identities and other ray pattern elements, such as neurotransmitter usage, also may vary independently. A similar pattern of partial constraint and flexibility has been observed for variation in eyespots size in the butterfly Bicyclus anynana .
Two haplotypes of C. briggsae have been described  and variation in ray pattern follows haplotype structure . Strains in haplotype 1, including AF16, exhibit almost exclusively a derived ray pattern. Strains in haplotype 2, including HK104, exhibit derived and ancestral ray patterns at equal frequencies. One interpretation of these results is that full expression of the derived ray pattern never became fixed within haplotype 2. However, a C. briggsae-like ray pattern also has been reported for C. clavopapillata , another species within the Elegans-group. C. clavopapillata has not been observed since its first description and some authors have considered it and C. briggsae to be synonymous . If C. clavopapillata is distinct from C. briggsae, the posterior position of ray 3 and its frequent fusion with ray 4 may be ancestral for these two species. This would make the C. elegans-like ray pattern in haplotype 2 an atavistic character. It should be possible to discriminate between these two models either through the characterization of additional C. briggsae strains or through the redescription and molecular characterization of C. clavopapillata.
Regardless of their evolutionary history, haplotypes 1 and 2 provided an entrée to the genetics of morphological variation of ray pattern in C. briggsae. The relatively slight difference between the AF16 and HK104 phenotypes hid a wealth of genetic variation. This was evident in the nearly continuous variation exhibited in RILs for both the position of ray 3 and its fusion with ray 4. This variation included many RILs with phenotypes more extreme than either parental strain. Such transgressive segregation is common in both plants and animals and is thought to arise through fluctuating selection and/or through stabilizing selection at minor QTL when directional selection at major QTL overshoots a phenotypic optimum . The transgressive segregation of ray pattern phenotypes may have resulted from selection on homeotic gene expression patterns. In C. elegans, ray 3 precursor cells are born at the junction of the mab-5 and egl-5 expression domains [23, 47]. These homeotic genes are required for the specification of positional identities in the posterior body and tail regions, respectively [47, 48] and some mutations in them cause the C. elegans ray pattern to phenocopy that of C. briggsae [22, 26]. We have demonstrated a significant transgressive association between allelic variation at Cb-egl-5 and variation in ray pattern. As Cb-egl-5 and Cb-mab-5 are closely linked, variation in either or both of these genes may be responsible for the observed association. Alternatively, linkage to Cb-egl-5 may be coincidental, and ray pattern variation in C. briggsae may not result from variation in homeotic gene expression patterns. The best test of these alternative models will be the high resolution mapping of the allelic variants responsible for ray pattern variation.
Loci not linked to the homeotic gene cluster also must be involved in ray pattern variation. Direct evidence for this was obtained from the mip-1 marker assisted introgression studies. The C. elegans homolog of mip-1, unc-22, is not linked to the the homeotic gene cluster and linkage of mip-1 to Cb-egl-5 and Cb-mab-5 is unlikely. There appear to be at least two loci that affect ray pattern linked to mip-1. One of these affected both the placement of ray 3 and its fusion with ray 4. The other affected only ray fusion. These associations were not transgressive, i.e. the allelic variants linked to mip-1 antagonized the allelic variants linked to Cb-egl-5. If the transgressive segregation linked to Cb-egl-5 does result from allelic variation in one or more homeotic genes, then the antagonistic variation linked to mip-1 may be in genes that regulate homeotic gene expression patterns. A direct test of this hypothesis is possible. Several genes required for proper regulation of homeotic gene expression patterns have been identified in C. elegans [25, 26, 37, 38, 49]. C. briggsae homologs of these genes could be tested for association with ray pattern variation in the RILs. Ideally, these tests would be integrated into a genome wide screen for variant loci with effects on ray pattern. This will require the enhancement of genetic resources available for C. briggsae.
Ray pattern in Caenorhabditis provides a powerful model for the study of morphological evolution. Macroevolutionary comparisons between species and microevolutionary analyses of variation within species are possible. Augmenting these approaches is a detailed understanding of the genetic and cellular basis of ray pattern development in C. elegans. In C. briggsae, intraspecific variants have been characterized that affect the expression of ancestral and derived ray patterns. These variants have a complex genetic basis involving multiple genes. Some of these genes exhibit transgenic segregation, some affect all of elements of ray pattern, and some that affect only a subset of ray pattern elements. At least one gene that affects ray pattern variation in C. briggsae is linked to the homeotic gene cluster. Thus, ray pattern variation may result from altered expression patterns of homeotic genes. Further characterizations of the genetics of ray pattern variation will test this model and will address interactions between different genes that impact ray pattern in C. briggsae.
Strains and strain maintenance
C. briggsae strains AF16, and HK104 are available from the Caenorhabditis Genetics Center . These strains were maintained on agar plates seeded with E. coli strain OP50. Recombinant inbred lines (RIL) were constructed starting with HK104 males mated to sperm-depleted AF16 hermaphrodites . Each RIL was initiated with a single F2 hermaphrodite and propagated through F11, one hermaphrodite per generation.
Ray pattern phenotypes were scored using differential interference contrast optics at a magnification of 400× . Right and left sides were scored independently . Microscopic images of worms anethesized in 0.2% sodium azide were digitally captured using a Spot Camera and Software (Diagnostic Instruments, Inc., Sterling Heights MI).
Forward and reverse primers for PCR amplifications Cb-egl-5, CAGGGAGCGGACAACTTCAAAGG and GGACACAGCCCAGGATTAGCGAC, respectively, were designed based on genome sequence data from C. briggsae strain AF16 . Amplification products were size fractionated by electrophoresis through 1% agarose.
Pearson's product moment correlation cofficients between ray pattern elements in RILs and Wilcoxon nonparametric tests of the association between Cb-egl-5 allelic variation with ray pattern variation were determined online at . Frequency distributions of the segregation of ray 3 positional and fusion phenotypes were compared using the Kolmogorov-Smirnov tests as implemented at . Ray pattern phenotypes of mip-1 introgressed strains were compared using reciprocal chi-squared tests using Excel v10.1.0 (Microsoft, Inc., Redman WA).
SEB: Planned and supervised all research activities. Participated in construction and genotyping of RILs. Reviewed all statistical analyses. Wrote manuscript.
CRD: Constructed, genotyped, and characterized ray pattern phenotypes of RILs. Statistical analyses of the segregation of ray pattern phenotypes and association of Cb-egl-5 variation with ray pattern variation. Reviewed manuscript.
JCB: Constructed and characterized phenotypes of mip-1-assisted introgressed lines. Statistical analyses of ray pattern phenotypes of mip-1 introgressed lines. Reviewed manuscript.
recombinant inbred line
quantitative trait loci
- dll :
- en :
- sal :
We thank R. Miller for sharing with us his unpublished data and J. Puglise and the reivewers of this manuscript for many helpful comments. This work was supported by NIH R15GM65847.
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