The MITF protein is a member of the MYC family of basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factors and is most closely related to the TFE3, TFEC, and TFEB proteins. In the mouse, MITF is required for the development of several different cell types, including the retinal pigment epithelial (RPE) cells of the eye. In Mitf mutant mice, the presumptive RPE cells hyperproliferate, abnormally express the retinal transcriptional regulator Pax6, and form an ectopic neural retina. Here we report the structure of the Mitf gene in Drosophila and demonstrate expression during embryonic development and in the eye-antennal imaginal disc. In vitro, transcriptional regulation by Drosophila Mitf, like its mouse counterpart, is modified by the Eyeless (Drosophila Pax6) transcription factor. In vivo, targeted expression of wild-type or dominant-negative Drosophila Mitf results in developmental abnormalities reminiscent of Mitf function in mouse eye development. Our results suggest that the Mitf gene is the original member of the Mitf-Tfe subfamily of bHLH-Zip proteins and that its developmental function is at least partially conserved between vertebrates and invertebrates. These findings further support the common origin of the vertebrate and invertebrate eyes.
EYE development in both vertebrates and invertebrates involves precise patterning and cell fate decisions that require the activities of several evolutionarily conserved transcription factors. Among these, the Pax6 gene provides a striking example (Quiringet al. 1994; Halderet al. 1995). The DNA-binding domains of Pax6 (paired box and homeodomain) are highly conserved through evolution and mutations in the gene affect eye development in species as diverse as humans, mice, and Drosophila (reviewed in Gehring and Ikeo 1999). In addition to Pax6, other genes expressed and/or required during early eye development are conserved between flies and vertebrates, including the transcription factors sine oculis, optix, eyes absent, and dachshund (reviewed in Wawersik and Maas 2000). Genetic, molecular, and biochemical investigations suggest that some of these nuclear factors assemble into transcriptional complexes and form a specific hierarchy involved in the establishment of a “retinal” fate. Studies performed in mammalian systems suggest that some of these regulatory relationships are conserved (reviewed in Wawersik and Maas 2000). Thus, early aspects of retinal development in both vertebrates and invertebrates may be regulated by a conserved set of transcription factors.
An important regulator of early eye development in the mouse is the microphthalmia-associated transcription factor (Mitf). The Mitf gene is a member of the MYC supergene family of basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factors (Hodgkinsonet al. 1993; Hugheset al. 1993) and can regulate target gene transcription through the canonical CANNTG E-box sequence (Hemesathet al. 1994). Mitf function is required not only during eye development but also in different cell types, including melanocytes, osteoclasts, and mast cells (reviewed in Moore 1995). Mitf has been shown to regulate genes controlling pigment synthesis, such as tyrosinase, tyrosinase-related protein-1 and -2 (reviewed by Goding 2000), osteoclast-specific genes, such as TRAP (Luchinet al. 2000) and cathepsin-K (Motyckovaet al. 2001), and mouse mast cell proteases (Kitamuraet al. 2000). Although the role of this gene during eye development has been characterized, no tissue-specific targets of Mitf have been identified.
The lack of Mitf function during mouse eye development results in reduced eye size or microphthalmia in the adult animal. In mouse embryos homozygous for loss-of-function mutations at the locus (such as Mitfmi-vga9 and Mitf mi-eyless-white), formation of the optic vesicle and cup occurs at the expected stage. However, the partitioning of the eye tissue into neural retina and retinal pigment epithelium (RPE) is disturbed, leading to the transformation of regions of the RPE into stratified neural retina; mutant RPE cells hyperproliferate and acquire columnar shapes as compared with the cuboidal shape observed in wild-type and form cells, which express neuroretinal marker genes (Nguyen and Arnheiter 2000). Thus, Mitf appears to play a role in the establishment of the RPE within the presumptive eye region.
Recently, it was shown that Mitf interacts with Pax6 in vitro, resulting in transcriptional inhibition (Planqueet al. 2001). The significance of these effects to in vivo gene function is unknown. During eye development the Mitf and Pax6 genes are initially expressed across the entire optic vesicle (including both presumptive retina and RPE regions) and are then restricted in expression such that Pax6 is expressed in neuroretinal cells while Mitf is restricted to RPE cells (Boraet al. 1998; Nakayamaet al. 1998; Nguyen and Arnheiter 2000). These expression patterns suggest that the transcriptional inhibition observed in vitro may be involved in determining neural vs. nonneural fate.
Here we report the identification of the Drosophila Mitf (Dmel/Mitf) gene and show that transcriptional activation by Drosophila Mitf is inhibited by Pax6 in vitro, similarly to the vertebrate proteins. Expression of Dmel/ Mitf in the developing fly eye raises the possibility that it is yet another conserved component in the genetic control of early eye development in fly and vertebrates. Moreover, its expression in the peripodial membrane, a tissue that is continuous with and overlies the presumtive retinal epithelium, suggests that peripodial and RPE tissue may be evolutionarily related. Targeted expression of wild-type and dominant-negative Mitf confirms a likely role for the gene in the development of eye-antennal disc derivatives. This evidence lends further support to the proposal that vertebrate and invertebrate eyes share a common origin.
MATERIALS AND METHODS
Dmel/Mitf genomic structure: The Drosophila melanogaster genome sequence (Adamset al. 2000) was available in GenBank through the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov) and was searched using tBLASTn (Altschulet al. 1990). Using the bHLH domain of the mouse Mitf gene, a Drosophila genomic region was identified (within clone AE003163) that showed considerable homology to the mouse Mitf sequence. By using the resulting Drosophila genomic region in a further blast search, several cDNA clones were identified. The Berkeley Drosophila Genome Project cDNA clones LP03467 and LD45277 showed considerable identity to the genomic sequences and were obtained and sequenced in full. Clone LD45277 turned out to be a full-size clone, which included a 5′ ATG with a continuous open reading frame as well as the poly(A) tail of a mature mRNA. The other cDNA clone (LP03467) was a chimeric clone containing the 5′ part of Mitf and a totally unrelated cDNA. By blasting the full-length LD45277 cDNA against the Drosophila genome, the structure of the Drosophila Mitf gene was reconstructed; the 5′ exon 1 was discovered on genomic clone AE003846, which encodes the first 153 nucleotides of the cDNA. This exon had been annotated as a possible open reading frame and had received the identification number CG17469. Clone AE003846 had been assigned to the chromosome 4 region 102E-F, while genomic clone AE003163, which contains the rest of the Dmel/Mitf coding region, has yet to be assigned a chromosomal location. On the basis of this, we presume that the Dmel/Mitf gene is located on chromosome 4.
Cotransfection studies: The full-length Drosophila Mitf cDNA as well as the Mitf EA mutant version were cloned into the pCDNA3.1 eukaryotic expression vector. In MitfEA, the negatively charged glutamic acid (E) within the basic region is changed to a neutral alanine (A). The mutation was created using mutagenic primers and a two-step PCR approach (Hoet al. 1989). The clone was then ligated into the BglII-XhoI-digested pcDNA3.1 vector. The reporter construct MBpluc contains six tandem M boxes (generously donated by Kenji Kasai); each M box contains an E box, which Mitf can bind to and from which it can activate transcription. For performing the assay, 293 cells were grown to 80% confluency (as judged by eye) in six-well plates in Dulbecco's Modified Eagle's Medium (DMEM) with fetal BSA but without antibiotics. Before transfection, the BSA was washed off using DMEM and the cells were then transfected using LipoFectamin-PLUS (Invitrogen, San Diego) according to manufacturer's instructions. Each pool of DNA was transfected in triplicate and the luciferase activity assayed using the Promega dual luciferase kit on a Wallac Victor2 luminometer (Perkin-Elmer Life Sciences), 12 hr after transfection. For normalizing the assay, a cytomegalovirus-driven Renilla luciferase was used. A total of 800 ng of each DNA was used and, where appropriate, empty pCDNA3.1 vector was used to bring the total amount of DNA to equal levels.
Expression analysis: Embryonic in situ hybridization was carried out with two different probes, a full-size probe made from the cDNA clone LD45277 and a shorter probe that lacks an MfeI fragment containing the basic helix-loop-helix leucine zipper domains. The latter probe was used to prevent false signals due to cross-reactions with other mRNAs coding bHLH-Zip proteins. The probe was labeled using the Boehringer Mannheim (Indianapolis) DIG RNA labeling kit according to instructions. Whole-mount in situs on embryos were performed according to Brody et al. (2002). Both probes resulted in the same expression pattern. Imaginal disc in situ hybridizations were also carried out with both probes, and no difference was seen between the two probes. The sense probe was used as a negative control and did not show any specific staining in either embryos or discs.
In vivo expression studies: A pUAS-MitfWT construct was generated by introducing the BglII-XhoI fragment of the LD45277 cDNA clone into BglII-XhoI-digested pUAST vector DNA (Brand and Perrimon 1993). For pUAS-Mitf EA, cloning into pUAST was at the NotI-XhoI sites and the Mitf sequence was mutagenized as described above (see Cotransfection studies). Transgenic lines carrying these constructs were generated by P-element transformation. Expression was achieved using the Gal4/UAS system (Brand and Perrimon 1993) by crossing Gal4 driver lines to flies carrying pUAS-Mitf WT or pUAS-Mitf EA transgenes as described in the results. Immunostaining with mouse monoclonal anti-ELAV Ab (Iowa Developmental Hybridoma Bank) was carried out using standard protocols (Wolff 2000). Few adult escapers were also observed in the cross to the ey-gal4 driver. These flies displayed eye phenotypes consistent with the effects seen in the developing discs, i.e., reduced eyes (pUAS-Mitf WT) and split or enlarged eyes (pUAS-MitfEA).
Sequence and genomic structure of the Drosophila Mitf gene: The Drosophila Mitf gene was identified by comparing the mouse Mitf amino acid sequence (bHLH domain) to the D. melanogaster genome sequence (Adamset al. 2000) translated in all six reading frames using tBLASTn (Altschulet al. 1990). The structure of the Drosophila Mitf gene is shown in Figure 1A. The gene covers at least 5.5 kb of genomic sequence. However, the total genomic size could not be determined due to a gap in the sequence in the intron between exons 1 and 2 (Figure 1A). At the adjacent ends of the two clones (A0E03846 and AE003164) are repetitive elements, which, when aligned, show an extensive sequence overlap. However, the end sequences of the two clones do not allow perfect alignment and all attempts at closing the gap using PCR have so far failed. The Dmel/Mitf gene is composed of nine exons, at least one of which is alternatively spliced (exon 4) as judged from comparing the two cDNA clones LP03467 and LD45277. Alternative splicing is a feature previously demonstrated to be both common and important for the mouse Mitf gene (Hallssonet al. 2000) as well as for other members of the mouse Mitf-Tfe family (Romanet al. 1991). The alternatively spliced isoforms (a and b) of Dmel/ Mitf maintain the same open reading frame and can therefore give rise to protein products that differ only in the first 19 amino acids of exon 4 (Figure 1A). No functional domains have been identified in this part of the protein and currently it is not clear if these splice forms represent functionally important alternative mRNAs.
By aligning the cDNA of Drosophila Mitf with mouse Mitf and considering the splice junctions, it can be seen that three of eight splice junctions present in the Drosophila cDNA are conserved between the two species. One of these is the splice junction between exons 2 and 3 in Drosophila (corresponding to exons 1B and 2 in the mouse counterpart). The other conserved junctions are between exons 6 and 7 and 7 and 8, which in both organisms contain the highly conserved basic and HLH domains (Figure 1A).
Conservation of the functional domains of the Mitf protein: The Dmel/Mitf gene encodes a 729-amino-acid protein, all exons included. This is considerably longer than the 525 amino acids encoded by the A form of the mouse Mitf gene, the longest known mouse form. Although overall amino acid homology is only 31%, certain domains of the protein have considerably higher conservation. As expected, the greatest amino acid homology between mouse and Drosophila is found in the bHLH-Zip domain. In both cases the basic domain is contained within exons 6 and 7; of 19 amino acids in this region, 17 are conserved between the two species. The 2 amino acids that differ are conservative substitutions: glutamate (at position 202) in the mouse vs. aspartate in Drosophila and leucine (at position 211) in the mouse vs. methionine in Drosophila (Figure 1B). The first helix of the HLH domain is completely conserved while in the loop 8 of 14 amino acids are conserved. A striking difference between the two proteins is the length of the loop. The mouse loop is 14 amino acids while in Dmel/Mitf it is 20 amino acids long. The second helix contains 16 amino acids and, of those, 11 are conserved between the two species. Interestingly, the leucine zipper of Dmel/Mitf consists of only two leucines while the mouse zipper is generally considered to consist of four. A possible explanation for this difference might be that the longer zipper evolved in vertebrates to increase the specificity of protein-protein interactions as more dimerization partners such as the related Tfe proteins became available. Although multiple differences exist between the Dmel/Mitf genes in D. melanogaster and D. pseudoobscura (data not shown), the bHLH-Zip domains are highly similar in the two species (Figure 1B). Comparing Drosophila Mitf to known homologs in other vertebrate species leads to the same conclusion as little diversity is found in the bHLH region of the protein. Species as diverse as humans and zebrafish show almost total conservation of the bHLH domains (Figure 1B).
Additional small regions of conservation are present outside the bHLH-Zip region. A block of amino acids at the amino terminus of the Dmel/Mitf protein shows considerable homology to the mouse A form, the splice version proposed to be the most ancient of the different Mitf transcripts in the mouse, also referred to as the eye-specific form (Amaeet al. 1998; Figure 1C). Included in this region is a glutamine-rich domain. Although no functional importance has been assigned to this portion of the protein, the conservation of the second splice junction supports the idea that this exon is conserved and may be relevant for normal protein function. A block of conserved amino acids is found in Drosophila exon 3 and shows homology to mouse exon 2A (Figure 1C). Of the first 30 amino acids of this exon, 17 are identical in the two proteins and 7 additional amino acids represent conservative substitutions. No particular function has been assigned to this region of the protein. The Dmel/Mitf counterpart to mouse serine 73, an amino acid shown to be phosphorylated by mitogen-activated protein (MAP) kinases in response to extracellular signals, is conserved. Furthermore, serine amino acids corresponding to both Ser298 and Ser409 are conserved even though not much conservation is found surrounding these amino acids (not shown). Close to the C terminus of the protein (25 amino acids from the end of mouse Mitf and 50 amino acids from the end of Dmel/Mitf) is a stretch of 6 conserved amino acids (DPLLSS). The function of these amino acids has not been determined. Finally, a short stretch of amino acids of Dmel/Mitf (DDIFDDIL) is remarkably similar to the DDVIDEII sequence, which in the TFE3 protein has been suggested to play a role in transcriptional activation (Beckmannet al. 1990). Although the similarity of these regions suggests functional importance, aligning the two regions creates a big gap in the overall alignment of Drosophila and mouse MITF proteins and thus decreases the overall homology of the alignment. Conservation of a domain may be more important than conservation of its exact location in the protein.
Dmel/Mitf functions as a transcriptional activator: Cotransfection experiments were performed to determine if the Drosophila Mitf gene can activate gene expression from promoter elements known to be regulated by the mouse and human Mitf genes. The wild-type Dmel/Mitf cDNA and a mutant version of Dmel/Mitf were cloned into the eukaryotic expression vector pCDNA3.1. The mutant version, MitfEA (arrow in Figure 1B, labeled EA), changes the most conserved amino acid within the DNA-binding domain. This amino acid is known to be essential for the DNA-binding ability of the related Tfeb protein and, since bHLH proteins are known to bind DNA as dimers, this mutation is thought to result in a dominant-negative protein (Fisheret al. 1993).
The constructs were cotransfected into 293T human embryonic kidney cells together with a reporter construct containing six tandem M boxes. The M box is an 11-bp sequence that contains an E box; the mouse Mitf protein is known to bind to and activate gene expression from this site. As can be seen from Figure 2A, the wild-type Drosophila Mitf construct is able to activate gene expression sevenfold compared to the empty vector, while the mutant version is unable to activate gene expression. Thus, clearly, the Drosophila MITF protein can activate gene expression from this regulatory element, just as the vertebrate factors do. Also, when the Mitf EA mutant version and wild-type Mitf constructs are cotransfected with the reporter, less activation is observed (Figure 2B), as would be expected if the EA mutant version acts in a dominant-negative fashion by interfering with DNA binding of the normal protein.
In cotransfection assays, the mouse MITF and PAX6 proteins interact and mutually inhibit transcription activation (Planqueet al. 2001). To test if this was also true for the Drosophila MITF and PAX6 (Eyeless) proteins, expression constructs containing the two genes were cotransfected into 293T cells together with the 6xM-box reporter construct and p300. As shown in Figure 2B, the presence of the ey gene interferes with the transcription activation potential of the Dmel/Mitf gene. We conclude that the function of Dmel/Mitf as a transcription activator is conserved between vertebrates and invertebrates, as is its potential interaction with Eyeless/Pax6.
Dmel/Mitf is expressed in the embryo and in the eye-antennal imaginal disc: To determine the expression pattern of Dmel/Mitf during Drosophila development, in situ hybridizations were carried out on embryos and eye-antennal imaginal discs. Two different probes were used, one representing the full-length cDNA and another lacking the bHLH-Zip region. The in situs revealed strong Dmel/Mitf expression in the precellular stages of embryonic development (Figure 3), representing maternally deposited Mitf message. As cellularization progresses, the amount of Mitf message decreases and is considerably reduced by gastrulation. During embryonic stages 9–11 expression is very low or undetectable. Expression then reappears by early stage 12 in the gut and stays high until stage 15, at which time the probe can no longer penetrate the embryo due to cuticular formation. Strong expression is seen in the epithelium of the midgut and hindgut, even though the possibility cannot be excluded that the signal is in the thin layer of visceral mesoderm surrounding the gut epithelium. No signal was detected using the sense control probe.
In the eye-antennal imaginal disc, Dmel/Mitf shows a dynamic pattern of expression during the second and third larval stages (L2 and L3). In L2 discs, Dmel/Mitf transcripts were detected throughout the eye region (Figure 4A). In L3 discs, Dmel/Mitf expression was restricted to two distinct domains. One expression domain lies between the eye and antennal regions (Figure 4B). The second domain (Figure 4C) is located in the region of the morphogenetic furrow (MF), where cells of the disc proper layer stop dividing and a subset commit to a neuronal fate. Posterior to the MF, cells do not divide and neurons differentiate into photoreceptors; anterior to the MF, cells are uncommitted and proliferating. In this second domain, Dmel/Mitf is expressed in the peripodial membrane, i.e., the cell layer that overlies the disc proper (inset in Figure 4C).
Expression of dominant-negative Dmel/Mitf in the larval disc interferes with eye development: To investigate the potential role of Dmel/Mitf in fly eye development, we expressed the wild-type (Mitf WT) or dominant-negative (MitfEA) forms in the developing eye-antennal disc. As expression of endogenous Dmel/Mitf appears to be restricted to the peripodial layer, we tested two Gal4 drivers to activate expression from UAS transgenes. The c311 driver (Gibson and Schubiger 2000; data not shown) expresses throughout the peripodial layer of the eye-antennal disc at the L2 stage and is still expressed in the peripodial membrane over the antennal region, but not the eye region, in late L3. The ey-Gal4 (Hazeletet al. 1998; Kenyonet al. 2003) driver expresses throughout the disc proper and peripodial cell layers until mid L2. Thereafter, expression is progressively lost from the antennal region and becomes restricted to the peripodial and disc proper layers of the eye region. In L3, ey-Gal4 expression decreases in the peripodial layer but continues to be robustly expressed in the disc proper. Both drivers are also expressed in other larval tissues. Expression of Drosophila MitfWT or MitfEA under the peripodial driver resulted in early larval lethality likely due to expression in tissues other than the imaginal discs. Larvae expressing Drosophila MitfWT or MitfEA under ey-Gal4 control most often died later and could be analyzed at the L3 stage. Expression of MitfWT resulted in eye-antennal discs with smaller eye regions but generally normal or nearly normal antennal regions. Neuronal morphogenesis, as detected by expression of the neural marker ELAV, was always reduced and occasionally absent (compare disc in Figure 5B to wild type in Figure 5A). On the contrary, the eye regions of discs expressing the MitfEA mutant protein were enlarged as compared to wild type and the developing photoreceptor field appeared correspondingly expanded (compare disc in Figure 5C to wild type in Figure 5A).
Here we describe the identification and initial characterization of Dmel/Mitf, the Drosophila homolog of the vertebrate bHLH-Zip transcription factor gene Mitf. Like its vertebrate counterpart, Dmel/Mitf can activate a known Mitf reporter in vitro and this transcriptional activation is sensitive to regulation by Eyeless/Pax6. Targeted expression of wild-type or dominant-negative forms of Dmel/Mitf results in opposite effects on the development of the eye-disc region and suggests that Mitf's role in eye development is at least partially conserved between fly and vertebrates. We discuss below the implications of this conservation at the molecular and developmental levels.
Conservation of Mitf at the DNA and protein levels: Despite extensive genome-wide searches for basic-helix-loop-helix proteins in the Drosophila genome, no Mitf or Mitf-related genes were found in previous analyses (Mooreet al. 2000; Peyrefitteet al. 2001). This suggests that the Dmel/Mitf gene described here is the only family member found in the Drosophila genome. This is in sharp contrast to vertebrate genomes, which, in addition to Mitf, contain the three other closely related genes Tfeb, Tfe3, and TfeC (discussed below). Furthermore, the zebrafish genome contains two Mitf genes (nacre/Mitfa and Mitfb; Lister et al. 1999, 2001) in addition to a presumed unknown number of Tfe genes. Other fish species, including Xiphophorus, Fugu rubripes, and Tetraodon nigroviridis, also contain two Mitf genes in their genomes, suggesting a gene duplication event in teleost fish after their separation from the bird/mammalian lineage (Altschmiedet al. 2002). Studies on Mitf function should therefore be greatly simplified in Drosophila as compared to studies in vertebrate species.
Within the MYC supergene family of basic bHLH-Zip transcription factors, the Mitf gene is most closely related to the Tfeb, Tfec, and Tfe3 genes. Together these four proteins form the Mitf-Tfe subfamily of bHLH-Zip proteins. All four proteins share almost identical basic regions and very similar HLH and Zip regions; the sequence is quite divergent outside these domains. It is likely that the Mitf gene is most closely related to the ancestral form of the Mitf-Tfe family of proteins since there are more similarities between Dmel/Mitf and the mouse Mitf genes than between Dmel/Mitf and any of the three Tfe genes (arrows in Figure 1B). For example, the mouse Tfec and Mitf genes differ at two positions in the helix 1 domain (YNINY in Tfec vs. FNIND in Mitf) whereas the mouse and fly Mitf genes are identical. Similarly, the mouse Mitf and Tfe3 genes are different in one position in the basic domain (LLKE in Tfe3 vs. LAKE in Mitf) and the Mitf and Tfeb genes are different in one position in helix 1 (LGML in Tfeb vs. LGTL in Mitf). All these residues are conserved in the mouse and fly Mitf genes, suggesting that the Mitf gene is the common ancestor and that the Tfe3, Tfeb, and Tfec genes arose from the ancestral gene after the separation of the vertebrate and invertebrate lineages.
The Drosophila Mitf protein is considerably larger than its vertebrate counterpart. In addition to the highly conserved bHLH-Zip domains, several other conserved regions were identified, suggesting that they represent regions of functional importance. These include a glutamine-rich region at the amino terminus, an amphipathic helical region with a transcription activation function, and a stretch of six amino acids at the carboxy end. In addition, a serine amino acid—which in the mouse MITF protein is phosphorylated by the MAP kinase pathway (Hemesathet al. 1998; Wuet al. 2000)—is also conserved in Dmel/Mitf. Thus, regulation of Dmel/Mitf function may involve phosphorylation at this site.
Significant differences also exist between vertebrate and fly Mitf. Most notably, in the mouse, an additional first exon (1M) codes for 11 amino acids and is included in a melanocyte-specific form of the Mitf mRNA, the M form. We have not been able to find sequences corresponding to exon 1M near the Dmel/Mitf gene. If we assume that the order of exons in the gene is conserved between mouse and Drosophila, then exon 1M would be situated between exons 2 and 3. However, the intron between exons 2 and 3 in Drosophila is only 51 nucleotides long and does not include an ATG. This lack of conservation is not unexpected. Vertebrate melanocytes originate from the neural crest, a cell lineage with no counterpart in Drosophila. Although the Drosophila eye does contain pigment cells, these arise from the eye-antennal epithelium and their pigment granules (ommochromes and drosopterins) are chemically distinct from the melanosomes (melanins) of vertebrates. Hence, fly pigment cells are not evolutionarily related to melanocytes. In this respect, exon 1M may reflect an evolutionary modification of the ancestral Mitf gene that arose specifically in the vertebrate lineage. Consistent with that, none of the related Tfe genes have an M-like exon, suggesting that this exon arose after the Tfe genes had arisen from the ancestral Mitf gene. Although the recently characterized Mitf gene of the ascidian Halocynthia roretzi is expressed in pigment lineage blastomeres, it does not appear to contain sequences that resemble exon 1M (Yajimaet al. 2003). Interestingly, the ascidian Mitf gene is expressed maternally, like its Drosophila counterpart.
RPE vs. peripodial epithelia—a case of common ancestry? The Mitf gene is expressed in the mouse eye during the optic vesicle and optic cup stages of eye development and is required for the normal formation and maintenance of the RPE. The RPE is a single layer of cuboidal cells, which basally displays numerous infoldings while apically abundant microvilli enclose and interdigitate with rod outer segments (Braekevelt and Hollenberg 1970; Braekevelt 1988, 1990). In Mitfmi/mi mutant mice, the RPE apical microvilli are absent and elongated rod outer segments do not develop (Bumstedet al. 2001). During development, the retina and RPE cell layers are closely juxtaposed and recent evidence supports an early role for the RPE in morphogenesis of the neural retina. Genetic ablation of the RPE cells early during eye formation prevents lamination of the retina, and later ablation results in loss of laminar organization (Raymond and Jackson 1995). In addition, factors secreted by the RPE have been shown to positively influence the development and maintenance of normal retinal morphology (Gauret al. 1992; Sheedloet al. 1992; Sheedlo and Turner 1998; Jablonskiet al. 2000). Thus, the RPE is thought to be a source of signaling molecules that lead to proper patterning and maintenance of the vertebrate retina.
The Drosophila eye, albeit structurally very different from the mouse eye, also develops from a bilayered epithelial structure. The progenitor epithelium that gives rise to the adult fly eye and associated head cuticle consists of a flattened sac with a columnar “disc proper” cell layer (from which the retina develops) and a noncolumnar “peripodial” cell layer (from which mostly cuticle, or epidermis, will form). Until recently the peripodial cell layer was not thought to be directly involved in retinal morphogenesis and it does not in fact contribute directly to any part of the adult eye (as mentioned above, these cells give rise to head cuticle). However, two groups (Choet al. 2000; Gibson and Schubiger 2000) have recently shown that peripodial cells are in fact required for proper development of the retina. In addition, Schubiger and colleagues (Gibson and Schubiger 2001; Gibsonet al. 2002) have shown that cellular projections, named “transluminal” projections, extend from one layer to the other and provide a mechanism for direct interactions between these two layers. Thus, it is now thought that signaling occurs between cells of peripodial and disc proper layers and that these interactions are essential for proper retinal development. The expression of Dmel/Mitf in the peripodial cell layer, specifically in the portion of the peripodial membrane that overlooks the site of photoreceptor neuron formation (MF), suggests that Mitf may be involved in this process.
To investigate the potential role of Dmel/Mitf in eye development, we expressed the wild type and dominant-negative Mitf EA mutant in the developing eye-antennal disc. Discs expressing wild-type Dmel/Mitf were variably reduced in size and neuronal morphogenesis was always reduced and occasionally absent. On the contrary, discs expressing the Mitf EA mutant version were larger than wild-type discs and the developing photoreceptor field appeared correspondingly expanded. The striking effect on disc size likely reflects changes in proliferation, whereas the variation in neuronal field size may be secondary to this or result from effects on primordia formation (cuticle/peripodial vs. eye) within the epithelium. As vertebrate Mitf has been implicated in proliferation and RPE specification (Nguyen and Arnheiter 2000), our observations strongly suggest significant conservation of Mitf's role in eye development. Further investigation of Dmel/Mitf function awaits the generation of Dmel/Mitf mutant alleles and better peripodial-specific drivers. Nonetheless, the similarities we have uncovered between the peripodial membrane of the fly eye-antennal disc and the RPE of the vertebrate optic vesicle/cup are very intriguing. The expression of Mitf in both epithelia raises the possibility that these tissues are evolutionarily related. In such a scenario, the ancestral tissue from which the eye eventually formed may have already displayed a partition into two fields: a nonneural Mitf+/Pax6– field and a neural Mitf–/Pax6+ field. Moreover, development of these two fields may have already involved inductive events between juxtaposed cell layers. Parallel investigations of Mitf function in mouse and fly will provide useful insights in evaluating these hypotheses.
Decene for assistance with fly genetics and immunostaining, the Bloomington Drosophila Stock Center for fly stocks, and the Iowa Developmental Hybridoma Bank for antibodies. This work was supported by a grant from the Icelandic Research Council, the Helga Jonsdottir and Sigurlidi Kristjansson Memorial Fund, the University of Iceland Science Fund (E.S. and J.H.H.), The Ruth and Milton Steinbach Fund (F.P.), and the Massachusetts Lyons Eye Research Fund (F.P.). F.P. is a recipient of the Research to Prevent Blindness Career Development Award and National Institutes of Health grant R01 EY13167 from the National Eye Institute.
Sequence data from this article have been deposited with the EMBL/GenBank Data Libraries under accession no. AY271259.
Communicating editor: C. A. Kozak
- Received July 23, 2003.
- Accepted January 20, 2004.
- Copyright © 2004 by the Genetics Society of America