The combined effect of two mutations that alter serially homologous color pattern elements on the fore and hindwings of a butterfly
© Monteiro et al; licensee BioMed Central Ltd. 2007
Received: 15 December 2006
Accepted: 11 May 2007
Published: 11 May 2007
The ability for serially homologous structures to acquire a separate identity has been primarily investigated for structures dependent on Hox gene input but is still incompletely understood in other systems. The fore and hindwings of butterflies are serially homologous structures as are the serially homologous eyespots that can decorate each of these wings. Eyespots can vary in number between fore and hindwings of the same individual and mutations of large effect can control the total number of eyespots that each of the wings displays. Here we investigate the genetics of a new spontaneous color pattern mutation, Missing, that alters eyespot number in the nymphalid butterfly, Bicyclus anynana. We further test the interaction of Missing with a previously described mutation, Spotty, describe the developmental stage affected by Missing, and test whether Missing is a mutant variant of the gene Distal-less via a linkage association study.
Missing removes or greatly reduces the size of two of the hindwing eyespots from the row of seven eyespots, with no detectable effect on the rest of the wing pattern. Offspring carrying a single Missing allele display intermediate sized eyespots at these positions. Spotty has the opposite effect of Missing, i.e., it introduces two extra eyespots in homologous wing positions to those affected by Missing, but on the forewing. When Missing is combined with Spotty the size of the two forewing eyespots decreases but the size of the hindwing spots stays the same, suggesting that these two mutations have a combined effect on the forewing such that Missing reduces eyespot size when in the presence of a Spotty mutant allele, but that Spotty has no effect on the hindwing. Missing prevents the complete differentiation of two of the eyespot foci on the hindwing. We found no evidence for any linkage between the Distal-less and Missing genes.
The spontaneous mutation Missing controls the differentiation of the signaling centers of a subset of the serial homologous eyespots present on both the fore and the hindwing in a dose-dependent fashion. The effect of Missing on the forewing, however, is only observed when the mutation Spotty introduces additional eyespots on this wing. Spotty, on the other hand, controls the differentiation of eyespot centers only on the forewing. Spotty, unlike Missing, may be under Ubx gene regulation, since it affects a subset of eyespots on only one of the serially homologous wings.
Modularity of body plans, and of serially repeated structures is widespread in the animal kingdom . Examples of modular structures include vertebrae , teeth , limbs , digits , arthropod body segments , C. elegans terminal rays , insect fore and hindwings [8–10], and butterfly eyespot patterns [11–13]. One of the key questions driving research in the field of modularity is to understand how such modules acquire the ability to differentiate into more or less distinct structures [14–16]. This differentiation and specialization of repeated body parts has, in the case of arthropod's body segments, increased through evolutionary time  presumably facilitating the radiation of these organisms into different environments.
The two pairs of wings on a butterfly are serially repeated structures, as are several of the pattern elements present within each wing . Pattern elements such as eyespots, for instance, can occur in each of the wing subdivisions, the wing cells, delineated by veins. Nijhout  proposed that the diversity of butterfly color patterns seen today results from the presence or absence, or through the modification of the size, shape, color or position of these serially homologous pattern elements within each wing cell. While the Hox gene, Ultrabithorax (Ubx), appears to be responsible for allowing the hindwing to acquire different wing patterns from the forewing , the genes and mechanisms by which particular serially homologous elements within each wing can acquire a separate identity from the other elements, however, are still unknown. Here we analyze the phenotypic effects of two spontaneous mutations, Missing and Spotty that affect the development of two serially homologous eyespots independently of the remaining eyespots on the wings.
The nymphalid butterfly Bicyclus anynana normally displays two marginal eyespots on both the dorsal and ventral sides of the forewing and seven eyespots on the ventral hindwing. Spontaneous [19, 20] and X-ray induced mutations  can alter the number of eyespots that appear on the wings surfaces, producing substantial departures from the wild type pattern. The spontaneous mutation Spotty was previously shown to be a single segregating factor of codominant effect . Spotty homozygotes have two extra eyespots on both the ventral and dorsal surfaces on the forewings of B. anynana. These extra eyespots occur in wing cells between those carrying the wildtype anterior and posterior eyespots. Spotty heterozygotes have either reduced sizes for both extra eyespots, or have one of the eyespots missing and the other eyespot present but reduced in size. This mutation, despite only having been analyzed in a qualitative fashion, appears to show a very localized effect in controlling the eyespot developmental program in a subset of the wing cells. Missing is a new spontaneous mutation that has a very similar phenotype to another x-ray induced mutation, 3+4, previously described . Contrary to Spotty, this mutation removes two eyespots from the hindwing, but the wing cells affected by Missing are homologous to those affected by Spotty on the forewing.
Here we investigate the phenotypic effects of Missing when crossed with either Missing, wildtype, or Spotty in order to describe the mutation in homozygote and in heterozygote condition and also to investigate whether Missing and Spotty, which when in isolation only seem to affect the hindwing or forewing pattern, respectively, show any interaction when placed together in the same individual. We additionally test whether during the imaginal disc stage the Distal-less and Engrailed transcription factors are absent from the centers of the hindwing eyespots that don't develop in adults of the Missing stock. We select one of these genes, Distal-less, as a possible target of the Missing mutation, and test whether this candidate gene is associated to the Missing phenotype by means of a linkage association study.
Extreme missing individuals have low fitness
The effect of Missing on the hindwing
The effect of Missing on the hindwing.
Cross type (df = 2)
Sex (df = 1)
Family (df = 19)
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hw eye 2
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hw eye 6
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The effect of Spotty on the forewing
The effect of the Spotty mutation on the forewing was previously described by Brakefield and French , who concluded that this mutant had a codominant effect relative to Wildtype. Spotty homozygotes display two well-developed eyespots in positions 3 and 4 on the forewing, and heterozygotes display two intermediate sized eyespots at these positions, or sometimes a single smaller eyespot at either position 3 or position 4.
The effect of Missing on the forewing
The effect of Spotty on the hindwing
The effect of Spotty on the hindwing.
Cross type (df = 1)
Sex (df = 1)
Family (df = 8)
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The combined effects of Spotty and Missing on the forewing and on the hindwing
The effect of Missing on the forewing in a Spotty background.
Cross type (df = 1)
Sex (df = 1)
Family (df = 6)
fw eye 2
fw eye 3
fw eye 4
fw eye 5
The effect of Spotty on the hindwing in a Missing background.
Cross type (df = 1)
Sex (df = 1)
Family (df = 8)
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hw eye 2
hw eye 3
hw eye 4
hw eye 5
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We identified an informative SNP (C/A) in a recognition sequence for the Bse NI restriction enzyme (NCCAGT) in the Dll 5'UTR fragment analyzed for the four grandparents. The wildtype grandparent was homozygous CCCAGT and the Bse NI enzyme cut the amplified PCR fragment into two fragments, 451 bp and 239 bp long, respectively. The Missing grandparent was homozygous CCAAGT and thus was not cut by the Bse NI enzyme. The F1 male parent was an expected heterozygote (CCCAGT/CCAAGT) and had the expected heterozygote restriction pattern; whereas the Missing female that was crossed with the F1 male had a similar genotype as the Missing grandmother, and was not cut by the restriction enzyme.
We tested two hypotheses: 1) If the Dll polymorphism is linked to the Missing mutation then we expect to find the majority of backcross individuals with the smallest or with absent eyespots to be homozygote for the CCAAGT genotype and display the "no-cut" pattern; and the majority of the individuals with the largest eyespots to display the "heterozygote-cut" restriction pattern on the gel. 2) On the other hand if the Dll polymorphism is not linked to the Missing mutation then we expect approximately 50% of backcross individuals with the smallest eyespots to have the "no-cut" pattern, and 50% to have the "heterozygote-cut" pattern. The same frequencies will be expected for the individuals with the largest eyespots.
From the 15 individuals that were genotyped with the smallest eyespots (0.06 mm average diameter ± 0.02 mm SE) we obtained 7 individuals (2 females and 5 males) that were not cut by the enzyme, and 8 individuals (4 females and 4 males) that were cut by the enzyme. From the 15 individuals that were genotyped with the largest eyespots (0.51 mm average diameter ± 0.03 mm SE), 10 individuals (2 females and 8 males) were not cut by the enzyme, and 5 individuals (3 females and 2 males) were cut by the enzyme. These results clearly support the hypothesis of no linkage between Dll and Missing genes.
The series of crosses clearly show that Missing, is a co-dominant mutation that has the dramatic effect of removing or reducing the size of two eyespots on the hindwing when in homozygote and heterozygote condition, respectively. Missing has the additional effect of reducing the size of the eyespots present in a homologous position on the forewing. The subtle effect of the Missing mutation on the forewing is not easily observed by eye and was only borne out because of the detailed quantitative approach used here. Spotty, on the other hand, is a mutation that introduces two eyespots on the forewing, and has no effect on the size of the homologous eyespots on the hindwing.
Selector genes such as Ubx, that are expressed only on the hindwings of insects, including butterflies, have been shown to affect the size of eyespots on the hindwing relative to their homologous counterparts on the forewing . Ubx-dependent eyespot size changes in the butterfly Junonia (Precis) coenia involve quantitative changes both in the signaling component as well as in the response components of the eyespot differentiation mechanism . From our analysis it appears that the qualitative effect of the Spotty allele on eyespot number is also regulated in a Hox gene-dependent fashion. Spotty is selectively expressed in the forewing, but not in the hindwing, indicating that a putative hindwing repressor (such as Ubx) modulates the effect of this allele. On the other hand, the Missing allele appears to exert its action on the eyespot developmental program in a Ubx gene-independent fashion. Missing will affect the size of homologous eyespots in both forewing and hindwings simultaneously.
It still remains to be determined whether these two mutations are genetically linked, perhaps representing alleles of the same gene. Crosses performed between Missing and Spotty individuals, followed by backcrosses to Missing, Wildype, or Spotty, were performed in order to try and analyze the shape of the backcross distributions. The shape of these distributions would indicate the likely linkage status of the Missing and Spotty genes. If the distributions had a clear two-peaked shape, this would indicate likely linkage, and the presence of two main genotypic classes (M/S and M/M for backcrosses to Missing for instance). If, on the other hand, the distributions were more normally distributed, i.e, reflecting the sum of four normal distributions, each representing a genotypic class, centered around different mean values (M/M, +/+; M/M, S/+; +/M, +/+; and +/M, S/+), then this would indicate that Missing and Spotty were found either on different linkage groups, or in the same linkage group but far apart. Unfortunately, there were two major complications to the successful completion of these analyses. First, the backcross distribution of Missing/Spotty hybrids crossed to Missing produced a skewed distribution against the zero eyespot diameter along the x-axis, where a series of Missing-like individuals were clustered. These skewed distributions cannot be readily analyzed with standard mixture models. Second, there was a strong family effect in that while some families produced a strong two-peaked distribution, other families didn't.
The immunohistochemistry showed that the Missing mutation, similarly to the 3+4 mutation previously described , affects the complete differentiation of the group of signaling cells at the center of the future eyespots. The focal cells, marked by the domains of Dll and en expression, are either a small cluster or do not differentiate at all, and as a result, there is no signaling during the pupal stage of eyespot differentiation, no visible white pupil, and no color rings of scales on the adult wing.
Distal-less is known to be one of the first genes to be expressed in the eyespot pupils during the fifth instar larval wing disc stage [23–25]. In Drosophila, this gene is also the first gene to be expressed in the future position of the ventral appendages of the fly. It acts as a selector gene that works in a fairly context-independent fashion since its ectopic activation in the leg disk of Drosophila results in a complete leg duplication . Because of these similarities we decided to test whether a putative mutation in the regulatory region of this gene may be causing the Missing phenotype. The association study concluded that the Missing mutation is not linked to Distal-less. Alternative genes to test would include Notch, also shown to be expressed in the larval wing disc, in the eyespot foci, and recently shown to be expressed slightly earlier in development in these cells relative to Distal-less , or other genes involved in the focus differentiation pathway, but putatively already acting downstream of Dll and Notch (reviewed in [20, 27]). Given that we are looking for a single gene mutation, a more sensible approach to identify this gene in the future may be to take a positional mapping study, with markers positioned all along the genome, until a candidate genomic regions is found to be associated with the mutation. Progress in the development of genomic tools for Bicyclus may allow this to be done in the near future .
We described the phenotypic effects of two mutations that affect the development of two of the serial homologous eyespots present in both fore and hindwings of B. anynana. Both mutations have a co-dominant effect relative to their wild-type alleles. These mutations, however, differ in the way that they interact with putative selector genes, previously shown to influence both the signal and the response components of the eyespot developmental mechanism in homologous eyespots positioned either on the fore or on the hindwings. Spotty targets eyespots only on the forewing and, therefore, may be under Ubx gene regulation, whereas Missing has a Ubx-gene independent effect, and reduces the size of eyespots on both fore and hindwing. Both these mutation are acting quite early in the eyespot development pathway by affecting the differentiation of the central group of cells, the focus, responsible for early pupal signaling and differentiation of the concentric rings of colored scales in an eyespot [29, 30].
These two mutations highlight the ability of genes of large effect to affect subsets of serially homologous structures and give them a separate identity from the rest. It is still unclear, however, whether the ancestral condition for these serial homologues is that of separately controlled units, regulated by genes such as Spotty and Missing that have very discrete affects on eyespot development brought together to form a complete row of eyespots, or whether, on the other hand, eyespots appeared as a cohesive unit of similarly looking structures, one per wing cell, resembling the proposed Nymphalid Groundplan , that gradually gained separate regulatory control by the appearance of genes such as Spotty and Missing. Phylogenetic comparative methods may eventually be able to shed light on this question.
Summary of all the crosses performed between Spotty (S), Missing (M), and Wildtype (Wt) individuals.
# of offspring
Spotty (male) crosses:
S male (PmABC2) × Wt female (PfA2)
S male (PmABC3) × Wt female (PfA3)
S male (PmABC7) × Wt female (PfB7)
S-Wt hybrid male (PmB72) × Wt female (Pf72)
S-Wt hybrid male (PmB73) × M female (PfB73)
Wild type (male) crosses:
Wt male (PmDE2) × S female (PfD2)
Wt male (PmDE3) × S female (PfD3)
Wt male (PmDE3) × M female (PfE3)
Wt male × Wt female
Wt male × Wt female
Wt male × Wt female
Wt male × Wt female
Wt male × Wt female
Missing (male) crosses
M male (Pm1) × M female (Pf1)
M male (Pm4) × M female (Pf4)
M male (Pm6) × M female (Pf6)
M male (Pm7) × M female (Pf7)
M male (Pm11) × M female (Pf11)
M male (Pm14) × M female (Pf14)
M male (Pm15) × M female (Pf15)
M male (Pm16) × M female (Pf16)
M male (Pm18) × M female (Pf18)
M male (Pm20) × M female (Pf20)
M male (Pm21) × M female (Pf21)
M male (Pm22) × M female (Pf22)
M male (PmFGH2) × Wt female (PfF2)
M male (PmFGH3) × Wt female (PfF3)
M male (PmFGH4) × Wt female (PfF4)
M male (PmFGH5) × Wt female (PfF5)
M-Wt hybrid male (PmF51) × M female (PfF51)
M-Wt hybrid male (PmF52) × M female (PfF52)
M-Wt hybrid male (PmF55) × M female (PfF55)
M male (PmFGH2) × S female (PfG2)
M male (PmFGH3) × S female (PfG3)
M male (PmFGH5) × S female (PfG5)
M-S hybrid male (PmG27) × Wt female (PfG27)
M-S hybrid male (PmG28) × Wt female (PfG28)
M-S hybrid male (PmG51) × Wt female (PfG51)
M-S hybrid male (PmG56) × Wt female (PfG56)
M-S hybrid male (PmG59) × Wt female (PfG59)
M-S hybrid male (PmG511) × Wt female (PfG511)
M-S hybrid male (PmG112) × Wt female (PfG512)
M-S hybrid male (PmG55) × S female (PfG55)
M-S hybrid male (PmG33) × M female (PfG33)
M-S hybrid male (PmG35) × M female (PfG35)
M-S hybrid male (PmG36) × M female (PfG36)
M-S hybrid male (PmG53) × M female (PfG53)
M-S hybrid male (PmG54) × M female (PfG54)
M-S hybrid male (PmG57) × M female (PfG57)
M-S hybrid male (PmG58) × M female (PfG58)
M-S hybrid male (PmG513) × M female (PfG513)
M-S hybrid male (PmG514) × M female (PfG514)
M-S hybrid male (PmG515) × M female (PfG515)
The ventral pattern of forewings and hindwings was quantified by measuring the diameter of the black discs of all eyespots present on the ventral side of fore and hindwings along an axis parallel to the wing veins. Diameter measurements were done using the Tiff files in Object Image 1.62 . Data were later transferred to MS Excel version X.
Analyses of variance for eyespot size were performed by asking whether there was a significant size difference for any of the forewing or hindwing eyespots (analyzed individually) between offspring from different types of cross (Missing × Wildtype, Wildtype × Wildtype, etc). Cross type was used as a fixed factor. For all analyses sex was also used as a fixed factor, since males are usually smaller than females and also have smaller eyespots, and family was coded as a random factor, nested within cross type. Analyses were done using SPSS version 11 for the Macintosh. Regression analyses were done in Excel version X for the Macintosh. Graphics were done is SPSS and in Excel.
Late fifth instar larval wings of Missing individuals were stained according to the protocol described in  with antibodies targeting Distal-less (a gift from Grace Boekhoff-Falk ) and Engrailed (antibody 4F11, a gift from Nipam Patel ).
An additional cross was performed between a Wildtype male and a Missing female, followed by a backcross of a single F1 male offspring to another Missing female. The bodies of these individuals were separated from the wings, placed in 2 ml screw cap vials filled with 100% ethanol, and stored at -70°C. Hindwings for all the backcross progeny were photographed, and the diameter of eyespots at positions 3 and 4 was measured and averaged for each individual. DNA was extracted from the four parents, and a 690 bp 5'UTR fragment, from the previously cloned Distal-less (Dll) gene  was amplified with the following two primers: Dll-NF1 (5'-CGCGAGTTGGTTGTGTCGGGTTACCTCGGA-3') and Dll-R6 (5'-CGTGGAAACACAGCATCACTATCACA-3'). PCR amplification conditions were 5 min at 94°, followed by 35 cycles of 40 sec at 94°C, 40 sec at 57°C, and 60 sec at 72°C. The amplification ended with a 5 min final extension period at 72°C. The PCR product was inserted into pGEM-T vector (Promega) and cloned in E. coli JM109 cells. Five clones were sequenced from each of the four parents and the sequences were screened for the presence of an informative polymorphic marker, i.e, a marker with two alleles and with a different allele, ideally in homozygote condition, present in the Missing and Wildtype grandparents. This marker should also be easily genotyped by means of an enzymatic essay where homozygote and heterozygote individuals can be differentiated by their restriction-digest banding pattern. The backcross generation was genotyped by first extracting DNA from the most extreme 15 individuals from each of the two ends of the eyespot size distribution. The same Dll fragment was amplified via PCR from these individuals, purified using a Quiagen PCR purification column, and then digested overnight with BseNI (BsrI) restriction enzyme following the manufacture's directions (Fermentas). Digested DNA was run on a 1.5% agarose gel, photographed, and the genotype was assayed from the restriction pattern.
We thank Daniel Gaile for statistical advice; Els Schlattman, Bert de Winter, Niels Wurzer, and Dennis Pietras for plant husbandry; Nipam Patel and Grace Boekhoff-Falk for the anti-En and anti-Dll antibodies, respectively; Human Frontier Science Program award RG0058 for financial support to AM and HJP; and NSF award IBN-0316283 for financial support to BC, LCS, LV, and ABV.
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