Fgf-dependent otic induction requires competence provided by Foxi1 and Dlx3b
BMC Developmental Biology volume 7, Article number: 5 (2007)
The inner ear arises from a specialized set of cells, the otic placode, that forms at the lateral edge of the neural plate adjacent to the hindbrain. Previous studies indicated that fibroblast growth factors (Fgfs) are required for otic induction; in zebrafish, loss of both Fgf3 and Fgf8 results in total ablation of otic tissue. Furthermore, gain-of-function studies suggested that Fgf signaling is not only necessary but also sufficient for otic induction, although the amount of induced ectopic otic tissue reported after misexpression of fgf3 or fgf8 varies among different studies. We previously suggested that Foxi1 and Dlx3b may provide competence to form the ear because loss of both foxi1 and dlx3b results in ablation of all otic tissue even in the presence of a fully functional Fgf signaling pathway.
Using a transgenic line that allows us to misexpress fgf8 under the control of the zebrafish temperature-inducible hsp70 promoter, we readdressed the role of Fgf signaling and otic competence during placode induction. We find that misexpression of fgf8 fails to induce formation of ectopic otic vesicles outside of the endogenous ear field and has different consequences depending upon the developmental stage. Overexpression of fgf8 from 1-cell to midgastrula stages leads to formation of no or small otic vesicles, respectively. Overexpression of fgf8 at these stages never leads to ectopic expression of foxi1 or dlx3b, contrary to previous studies that indicated that foxi1 is activated by Fgf signaling. Consistent with our results we find that pharmacological inhibition of Fgf signaling has no effect on foxi1 or dlx3b expression, but instead, Bmp signaling activates foxi1, directly and dlx3b, indirectly. In contrast to early activation of fgf8, fgf8 overexpression at the end of gastrulation, when otic induction begins, leads to much larger otic vesicles. We further show that application of a low dose of retinoic acid that does not perturb patterning of the anterior neural plate leads to expansion of foxi1 and to a massive Fgf-dependent otic induction.
These results provide further support for the hypothesis that Foxi1 and Dlx3b provide competence for cells to respond to Fgf and form an otic placode.
The vertebrate inner ear provides auditory and vestibular functions and develops from the otic placode, a transient thickening of head ectoderm adjacent to the developing hindbrain. In zebrafish the otic placode cavitates to form the otic vesicle also known as the otocyst, an epithelial structure with sharply defined borders, which later gives rise to the inner ear including its neurons and structural elements [1–4].
Studies in various species suggest that otic placode formation is a multi-step process. Cranial placodes, including the otic placode, arise from a common region, the preplacodal domain that extends around the anterior neural plate border. Formation of the preplacodal domain represents the earliest stage of placode induction and is regulated by multiple signaling pathways including Bmp, Wnt and Fgf [5–7]. Subsequently, Fgf signals from the adjacent hindbrain and underlying mesoderm induce cells within the preplacodal domain to form the otic placode (reviewed in [3, 8–10]). In zebrafish, Fgf3 and Fgf8 have been implicated as having overlapping functions in otic placode induction [11–13]. Both genes are expressed in the future hindbrain by late gastrula stages, and fgf3 is also expressed at this stage in the underlying mesendoderm. Loss of either fgf3 or fgf8 leads to a reduction in ear size and loss of both fgf3 and fgf8 together results in near or total ablation of otic tissue. In mouse, Fgf3 and Fgf10 act as redundant signals during otic induction [14, 15]. Fgf3 is expressed in the hindbrain region that abuts the preotic domain, whereas Fgf10 is expressed in the mesoderm beneath it; loss of both Fgf3 and Fgf10 results in complete ablation of otic development [14, 15]. Furthermore, Fgf8 has been shown to play a critical role upstream of the FGF signaling cascade required for otic induction in this species . In chick, Fgf3, Fgf8 and Fgf19 and in amphibians, Fgf2 and Fgf3 have been implicated in otic induction [16–20].
Misexpression studies indicate that Fgf signaling is not only necessary but also sufficient for otic induction [11, 13, 21–25]. However, the region where ectopic otic structures formed was inconsistent in these studies, ranging from limited induction in the region surrounding the endogenous ear [13, 21, 22] to widespread ectopic otic induction at the expense of other sensory organs [23–25]. Infection of chick embryonic hindbrain and surface ectoderm with an Fgf3-expression virus vector at early somite stages results in an enlarged otocyst and ectopic otic vesicles just anterior and posterior to the normal otic vesicle . Furthermore, implantation of beads coated with FGF8 or FGF2 close to the developing placode in the chick embryo at early segmentation stages produces a similar result . An enlarged otic placode and enlarged otic vesicle have also been reported in zebrafish after overexpression of Fgf8 by mRNA injections at the 2-cell stage and after implantation of FGF8-coated beads at shield stage . In contrast, injection of 8-cell stage zebrafish embryos with plasmid DNA containing fgf3 or fgf8 under the control of a constitutive promoter leads to early variegated misexpression of Fgf3 or Fgf8 and ectopic otic induction all around the anterior neural plate border at the expense of other sensory organs [23, 24]. Similar results were obtained in Medaka after misexpression of Fgf8 under the control of an artificial heat shock promoter at midgastrula stages . Treatment of zebrafish embryos with retinoic acid greatly expands the hindbrain expression domains of fgf3 and fgf8 and leads to Fgf-dependent formation of ectopic, supernumerary otic vesicles abutting the anterior neural plate .
Transplantation experiments suggest that competence of naive ectoderm to form an otic placode is initially widespread but becomes restricted to a region adjacent to the hindbrain by late gastrula or early neurula stages (reviewed in [26, 27]). We previously proposed that Foxi1 and Dlx3b may provide the molecular basis for this competence to form an ear . Expression of the homeobox gene, dlx3b, is initiated at the beginning of gastrulation on the future ventral side of the embryo and together with dlx4b, is restricted in late gastrula stage embryos to a stripe corresponding to cells of the future neural plate border. Expression of both genes is subsequently further restricted to cells of the future olfactory and otic placodes by the beginning of somitogenesis [29–32]. Knockdown of dlx3b and dlx4b together causes severe loss of otic tissue even in the presence of functional Fgf signaling, consistent with them playing a role to specify the competence of cells to form the ear [33, 34]. Expression of the forkhead winged helix transcription factor, foxi1, is initiated prior to gastrulation in the future ventral half of the embryo and is progressively restricted to bilateral regions including the preotic domain at late gastrula stages [35–37]. Disruption of foxi1 leads to severe defects in otic placode formation and highly variable ear phenotypes [36, 37] suggesting that foxi1 may also influence otic competence. Loss of both Dlx3b and Foxi1 together ablates all indications of otic induction even in the presence of a fully functional Fgf signaling pathway [24, 28]. BMP signaling may regulate early expression of both dlx3b and foxi1 because dlx3b is not expressed in bmp2b mutant embryos and overexpression of the Bmp-binding antagonist noggin by mRNA injection completely abolishes foxi1 expression [38, 39]. In addition to BMP, Fgf signaling has also been implicated as a regulator of foxi1, although the published results are inconsistent [23, 39, 40]; Phillips et al.  report that localized misexpression of fgf3 or fgf8 can induce high-level expression of foxi1 in the anterior head region, whereas Fürthauer et al.  and Kudoh et al.  show that Fgf signaling represses foxi1 expression.
Here we show that Fgf signaling has different consequences for otic induction depending upon the developmental stage. Due to its repression of non-neural ventral fate before and during gastrulation, Fgf activity early in development leads to ablation or reduction of otic tissue which is foreshadowed by the loss or reduction of dlx3b and foxi1, respectively. We demonstrate that neither dlx3b nor foxi1 is activated by Fgf signaling, but rather BMP signaling regulates dlx3b indirectly and foxi1 directly. Later at the end of gastrulation, however, activation of the Fgf signaling pathway leads to Dlx3b and Foxi1 dependent formation of ectopic otic tissue. Our results support the hypothesis that Foxi1 and Dlx3b provide competence for cells to respond to Fgf signaling and form an otic placode.
Misexpression of fgf8induces ectopic otic tissue within the normal otic field
It was recently shown that Fgf signaling is not only necessary but also sufficient for otic induction. Several studies showed that gain of Fgf function results in expanded or ectopic otic induction, however, the location and extent of this effect was inconsistent among the studies [13, 21–25]. Differences in the time during development that Fgf signaling was increased in these various studies might explain these inconsistencies.
To control the time of Fgf signaling precisely, we generated a stable transgenic line that allows us to express fgf8 uniformly under the control of the zebrafish temperature-inducible hsp70 promoter. We tested the reliability of the line by monitoring fgf8 expression in transgenic animals before and after heat shock at the end of gastrulation and at midsegmentation stages. Without heat shock, all embryos from a cross between heterozygous hsp:fgf8 and wild-type fish show the endogenous pattern of fgf8 expression. Following a 30 minute heat shock at either developmental stage, we observe strong and ubiquitous expression of fgf8 in 50% of the progeny. Expression levels of fgf8 under these conditions are very high and, thus, mask endogenous fgf8 expression (additional file 1). Ectopic fgf8 mRNA is gradually lost within approximately 180 minutes of its onset, indicating that heat shock leads to strong overexpression of fgf8 for a relatively short period of time (additional file 1).
Using this line and fgf8 mRNA injections, we subsequently examined the consequences of fgf8 misexpression at various times during development as indicated by, starmaker (stm) that is expressed throughout the otic vesicle epithelium from early vesicle stages. Overexpression of fgf8 by mRNA injection at the 1-cell to 2-cell stage leads to severe dorsalization and expansion of the neural plate at the expense of epidermal and preplacodal ectoderm; hence, embryos display severe reduction (32%) or complete loss (68%) of otic tissue (Fig. 1A,B and data not shown). Misexpression of fgf8 upon heat shock from late blastula through gastrula stages also causes dorsalization, and embryos show a reduction in the size of the otic vesicle (Fig. 1C,D,E). The size of the otic vesicle that forms is correlated with the time at which fgf8 is overexpressed. A very small vesicle forms after fgf8 misexpression before gastrulation, whereas later misexpression of fgf8 leads to larger otic vesicles. Larger than normal otic vesicles are produced after overexpression of fgf8 at the end of gastrulation or during early segmentation stages (Fig. 1F,G), and misexpression at the later time also frequently resulted in duplicated otic vesicles (data not shown). Misexpression of fgf8 at even later stages, such as the 8-somite stage, either has no effect on otic vesicle size or produces slightly smaller otic vesicles, presumably due to patterning defects (Fig. 1H). Although fgf8 misexpression during gastrulation appears to increase the number of cells fated for otic development, as evidenced by the increase in otic vesicle size, in no case did we observe signs of ectopic otic tissue outside of the normal ear field, that is, outside the field of cells that normally express the putative otic competence factors, dlx3b and foxi1. We also did not observe formation of ectopic otic vesicles at the expense of other sensory organs. Our results suggest that the ability of ubiquitously expressed Fgf8 to act as an ear inducing factor is restricted to times between the end of gastrulation and early segmentation and to the region where the ear normally forms.
Misexpression of fgf8 affects the expression of foxi1 and dlx3b
We and others recently showed that loss of both Foxi1 and Dlx3b together ablates all indications of otic induction even in the presence of a fully functional Fgf signaling pathway [24, 28]. Because both transcription factors are already expressed by gastrulation stages, we hypothesized that otic vesicle loss or reduction after fgf8 overexpression might be due to compromised expression of foxi1 and/or dlx3b. To test this hypothesis, we induced misexpression of fgf8 at various times and then fixed embryos at late gastrulation stages when Fgf-dependent otic induction begins. Overexpression of fgf8 by mRNA injection at the 1-cell stage, which prevents otic vesicle formation, frequently (90%) leads to embryos showing a complete loss of foxi1 and dlx3b (Fig. 2A,B,F,G). Misexpression of fgf8 at late blastula or early gastrulation stages, which results in smaller otic vesicles at later stages, causes reduced expression of both foxi1 and dlx3b, showing again a strong correlation between the onset of fgf8 overexpression and the size of the foxi1 and dlx3b expression domains (Fig. 2C,D,F,H,I).
The effect of Fgf8 on Foxi1 and Dlx3b expression is probably due to its early role in dorsoventral patterning. It was recently shown that the balance between Fgf and Bmp signaling regulates dorsoventral patterning of the zebrafish embryo into prospective neural and epidermal domains [39–41]. Furthermore, recent results suggest that Fgf induced activation of MAP kinase is able to interfere with Bmp signaling by phosphorylation of specific residues in the linker region of Smad1, leading to Smad1 inactivation [42, 43]. We find that after overexpression of fgf8, the reduced foxi1 and dlx3b expression domains still overlap p63, an epidermal marker, and are complementary to sox3, a neural marker (data not shown). This indicates that ectopic activation of Fgf signaling at late blastula or early gastrulation stages is still able to activate neural fate at the expense of epidermal fate, hence reducing the size of the foxi1 and dlx3b expression domains. Additionally, foxi1 or dlx3b are not expressed ectopically as can happen after localized Fgf misexpression .
To provide further insight into the role of Fgf8 signaling in Foxi1 and Dlx3b patterning, we treated wild-type embryos from late blastula stages until the end of gastrulation with SU5402, a specific inhibitor of the tyrosine kinase activity of all Fgf receptors . We find that SU5402, at a concentration of 40 μM, blocks expression of the Fgf-dependent gene, sprouty4, (data not shown) indicating that inhibition is complete. Nevertheless, expression of both foxi1 and dlx3b is unaffected by the inhibitor (Fig. 2E,J). These results show that Fgf signaling is able to repress foxi1 and dlx3b expression but is not required for their initial activation.
Early Bmp signaling activates foxi1 directly and dlx3bindirectly
Our fgf8 overexpression studies showed that foxi1 and dlx3b are negatively regulated in dorsal ectoderm by Fgf signaling, raising the possibility that Bmp signaling might activate these genes in the ventral ectoderm. In support of this idea, we find that neither foxi1 nor dlx3b is expressed in bmp2b mutants (data not shown) and their expression is strongly reduced in bmp7 mutants (Fig. 3A,B,F,G). We also observe the same phenotype after knockdown of the ventralizing transcriptional repressors, Vox and Vent, by antisense morpholino oligonucleotides (Fig. 3C,H). Furthermore, overexpression of Bmp2b by mRNA injection expands expression of foxi1 and dlx3b at the expense of anterior neural plate (Fig. 3D,E,I,J).
To learn whether foxi1 and dlx3b are direct transcriptional targets of Bmp, we injected embryos at late blastula stages (sphere) with Bmp2a protein and raised them in cycloheximide (CHX), a protein synthesis inhibitor. As a positive control, we examined expression of vent, a direct target of Bmp signaling [45, 46]. As expected, vent is ectopically expressed after Bmp2a protein injection (Fig. 4I,J). Control or BSA-injected embryos treated with CHX have arrested gastrulation movements and do not exhibit vent expression (Fig. 4K). In CHX-treated embryos injected with Bmp2a protein, however, gastrulation movements are still blocked but vent expression is restored indicating that Bmp2a protein is sufficient for vent expression and de novo protein synthesis is not required (Fig. 4L). Both foxi1 and dlx3b behave similarly to vent with ectopic or missing expression after Bmp2a protein injection or CHX treatment, respectively (Fig. 4A–C, E–G). However, after Bmp2a protein injection and CHX treatment, foxi1 expression is restored, like vent, whereas dlx3b expression is not (Fig. 4D,H). Thus, our results suggest that Bmp signaling activates both foxi1 and dlx3b expression. Furthermore, as early as sphere stage, foxi1, but not dlx3b, acts as a direct transcriptional target of the Bmp signaling pathway.
Misexpression of fgf8at late gastrulation stages leads to expanded induction of otic markers within the preotic field
To understand how overexpression of fgf8 at the end of gastrulation or early segmentation stages leads to the formation of much larger otic vesicles, we examined early markers of otic induction. First, to learn whether all cells receive the ectopic Fgf signal, we examined expression of two Fgf reporter genes, erm and pea3, members of the ETS family of transcription factors [47, 48]. We find that within 90 minutes after a 30 minute heat shock at the end of gastrulation or during early segmentation stages, essentially all cells of the transgenic embryo respond to the ubiquitous Fgf signal whereas non-transgenic siblings are unaffected (Fig. 5B,C,H,H and data not shown). Expression of foxi1 that is restricted to two bilateral domains at this stage is again reduced, whereas dlx3b expression surrounding the anterior neural plate is unchanged (Fig. 5D,J and data not shown). This indicates that foxi1 but not dlx3b is presumably still under the control of Bmp signaling that is attenuated by the anti-Bmp activity of elevated Fgf8 in heat shocked transgenic embryos. In contrast to the reduced foxi1 expression, we find that expression of the early preotic marker, pax8, a paired box homeodomain gene, is expanded but only within the preotic region (Fig. 5E,K). In wild-type embryos at the one-somite stage, double labeling with both foxi1 and pax8 shows that preotic, Fgf-dependent pax8 is expressed only in part of the foxi1 expression domain [11–13, 36]. After exposure of the entire foxi1-positive domain to fgf8 in transgenic embryos, Foxi1 protein, present prior to the heat shock, presumably persists and supports the observed expanded pax8 expression. Because preotic pax8 expression depends completely on Foxi1, and foxi1 expression is restricted to two bilateral domains but is not expressed in other regions of the preplacodal domain at the end of gastrulation where we observe expanded pax8, we also examined expression of pax2a, another early marker of otic fate. pax2a expression depends partially on foxi1 and partially on dlx3b that is expressed in a stripe corresponding to cells of the future neural plate border, which presumably represents the entire preplacodal domain . As with pax8, we detect expanded pax2a expression but again only in the preotic region of heat shocked, transgenic embryos (Fig. 5F,L). Examination of sox9a expression , a third early otic marker, yields identical results with upregulation of sox9a only in the preotic region but not in other regions of the preplacodal domain of transgenic embryos (additional file 2C, F). Together, these results show that cells only in the preotic region are competent to embark upon the path towards otic fate even if Fgf signaling is strongly activated throughout the entire embryo.
Ectopic otic cells undergo normal ear development
Because the expression domains of pax8 and pax2a are expanded in the preotic region in the transgenic embryos, we examined whether these cells undergo normal development. We find that many more cells contribute to the otic placode in heat shocked, transgenic animals than in non-transgenic siblings (Fig. 6A,E). Nevertheless, the otic vesicle subsequently forms with no overt morphological differences other than its increased size. Both transgenic and non-transgenic embryos form two otolith seedlings and no size difference can be observed after three days of development (Fig. 6B,F and additional file 3). Moreover, patterning of the otic vesicle developed normally as indicated by fgf8, hmx3 and follistatin that demarcate anteroposterior domains, by dlx3b, otx1 and wnt4 in dorsoventral domains and by pax2a that highlights mediolateral domains at 24 h (Fig. 6C,D,G,H and data not shown).
Foxi1 and Dlx3b both participate in expanded otic induction
Because ectopic expression of pax8 and pax2a, in response to overexpression of fgf8, is confined to the preotic region and overlaps with the expression domain of foxi1 but not dlx3b, it is possible that ectopic induction depends exclusively on Foxi1. We recently showed that depletion of Foxi1 or Dlx3b alone results in formation of a reduced otic vesicle and that removal of both factors leads to complete failure of otic specification . We thus examined the response of embryos to fgf8 overexpression in the absence of either Dlx3b or Foxi1. We find that overexpression of fgf8 at the end of gastrulation rescues the small otic vesicle generated by compromised Dlx3b function (Fig. 7A,B,E,F). Surprisingly however, we also detected partial rescue by misexpression of fgf8 in embryos depleted of Foxi1 (Fig. 7C,G). Consistent with our previous results , we are unable to detect any sign of otic specification after loss of both factors, Foxi1 and Dlx3b, even if Fgf signaling is significantly increased (Fig. 7D,H). Taken together, our results show that either Foxi1 or Dlx3b is required for cells to be competent to respond to Fgf8 signaling and subsequently form the ear. Loss of either Foxi1 or Dlx3b can be partially compensated by an increase in Fgf signaling, but removal of both leads to complete loss of otic fate.
Ectopic foxi1provides competence for ectopic Fgf-dependent otic induction
To examine whether Foxi1 expression is sufficient for cells to be competent to adopt an otic fate, we used several different approaches. Misexpression of foxi1 by mRNA or plasmid injections at the 1- to 2-cell stage in hsp:fgf8 embryos or transplantation of foxi1 positive cells into hsp:fgf8 host embryos followed by heat shock at late gastrulation stages were inconclusive (data not shown). Instead, we used retinoic acid (RA) treatment to expand the foxi1 expression domain. Application of high doses of RA (1 μM) results in expansion of the hindbrain expression domains of fgf3 and fgf8 throughout the anterior neural plate and massive, Fgf-dependent expansion of the pax8 expression domain . We find that a much lower concentration of RA (20 nM) is sufficient to expand pax8 expression around the anterior border of the neural plate (Fig. 8A,E). Embryos treated with 20nM RA show no change in otx2, fgf3, fgf8 or sox9a expression, indicating that this RA concentration does not posteriorize the anterior neural plate or expand posterior expression domains (Fig. 8 and additional file 2). Consistent with this, RA treated wild-type embryos show no loss of anterior structures but develop enlarged otic vesicles at 1 and 2 days of development (unpublished results). At the end of gastrulation, dlx3b expression in RA treated embryos is indistinguishable from untreated embryos (data not shown), whereas the foxi1 expression domain is greatly expanded. We find that foxi1 is no longer limited to the two bilateral domains but instead expands into the entire preplacodal domain similar to the dlx3b stripe surrounding the anterior neural plate (Fig. 8B,F,). In wild-type embryos, pax8 expression depends upon Fgf signaling [11–13], as confirmed by use of fgf3, fgf8 double mutants (Fig. 8C). In fgf3, fgf8 double mutants treated with RA, pax8 expression is greatly reduced, although we find some residual anterior expression (Fig. 8G), suggesting that a remaining Fgf (perhaps Fgf24, Fgf17a or Ff17b; [49–51]) may provide inductive signaling for pax8 expression in this region. In foxi1 mutants preotic pax8 expression is completely abolished, whereas in RA treated foxi1 mutants pax8 expression is largely gone, although surprisingly we find some residual expression at the anterior end (Fig. 8D,H). Depletion of Dlx3b and Dlx4b by morpholino injections in RA-treated foxi1 mutants did not further reduce pax8 expression and we also could not detect any ectopic expression of the three known members of the zebrafish Foxi class genes, foxi2, foxi3a and foxi3b (data not shown). The persistence of some residual pax8 expression in RA treated foxi1 mutant embryos indicates that additional genes might be involved in otic induction in the presence of RA. However taken together, our results show that most of the ectopic otic induction in RA treated embryos is due to the presence of ectopic Foxi1.
The competence of preotic cells to respond to Fgf-signaling is acquired at the end of gastrulation
Numerous loss of function and gain of function studies have led to the conclusion that Fgf signaling is necessary and sufficient for induction of the otic placode, although not all cells are competent to respond to the inductive signal. Our results add several pieces of evidence in support of our hypothesis  that competence results from expression of Foxi1 or Dlx3b transcription factors: 1) Cells become competent shortly after they start expressing the factors (Fig. 1). 2) Expanding the domain of Fgf signaling extends otic fate to cells that express the factors but normally see only low levels of signal (Fig. 6), but not to cells that never express the factors (Fig. 5). 3) Cells that ectopically express Foxi1 acquire competence (Fig. 8), whereas 4) cells that lose both factors lose competence (Figs. 1, 2, 3), even when Fgf signaling is elevated (Fig. 7).
Our results further show that there is only a relatively short time window for otic induction, between the end of gastrulation and early segmentation stages. Misexpression of fgf8 only within this period leads to formation of enlarged otocysts whereas overexpression earlier or later results in smaller or unchanged otic vesicles (Fig. 1). Smaller otic vesicles after misexpression of fgf8 up to midgastrulation stages is presumably due to the effects of Fgf signaling on dorsoventral patterning that subsequently affects expression of the Foxi1 and Dlx3b expression domains. Fgf and Bmp signals antagonistically control dorsoventral patterning of the embryo during gastrulation and are necessary to establish prospective neural and epidermal domains [39–41]. Consistent with this interpretation, we see that ectopic Fgf signaling leads to an expanded neural domain and a reduced epidermal domain (Fig. 2). The reduction in size of the epidermal domain results in smaller Foxi1 and Dlx3b expression domains, and, hence, reduced numbers of cells that are competent to form the ear (Fig. 9).
Foxi1 and Fgf signaling act together to regulate pax8expression
Transplantation experiments suggest that competence of naive ectoderm to form an otic placode is initially widespread during early gastrulation stages but becomes subsequently restricted to a relatively small area abutting the hindbrain at early segmentation stages [26, 27]. The expression patterns of the foxi1 and dlx3b genes show similar progressive restrictions during early development consistent with the proposed roles of Foxi1 and Dlx3b proteins as the molecular regulators of otic competence . Expression of both foxi1 and dlx3b is initiated prior to or at the beginning of gastrulation throughout the future ventral side of the embryo. Subsequently foxi1 expression is restricted to bilateral domains at the lateral edges of the hindbrain while dlx3b is restricted to a stripe of cells corresponding to the future neural plate border, including the preotic domain [29–32, 36, 37, 52]. Depletion of foxi1 or dlx3b leads to loss of otic tissue and the combined loss of both, Dlx3b and Foxi1, ablates all indications of otic induction even in the presence of a functional Fgf signaling pathway [24, 28, 33, 34]. The changes in foxi1 and dlx3b expression after misexpression of fgf8 up to midgastrulation stages (Fig. 2) foreshadows the loss of otic tissue, providing further evidence that these genes are required within the preotic region for otic induction. We never observe ectopic expression of foxi1 or dlx3b after misexpression of fgf8 and further demonstrate that foxi1 and dlx3b are positively regulated by Bmp signaling but not Fgf signaling (Fig. 2, 3).
These results contrast with a recent study that reported ectopic expression of foxi1 after Fgf misexpression . The conflicting results are presumably due to differences in the methods used to obtain ectopic Fgf signaling. Phillips et al.  injected 8-cell stage embryos with plasmid DNA encoding Fgf3 or Fgf8 under the control of a constitutive promoter. This leads to early variegated misexpression  of Fgf3 or Fgf8. With this technique, embryos exhibited some moderate dorsalization, but by co-labeling for neural markers and Fgf expression, the authors ensured that the analyzed embryos had only scattered patches of Fgf expressing cells and no overt signs of dorsalization. However, even with no overt signs of dorsalization, patchy activation of Fgf signaling during gastrulation creates local dorsalizing centers that subsequently alter gastrulation movements resulting in the formation of a partial secondary axis . Use of our hsp:fgf8 transgenic line also changes dorsoventral identity but due to strong, uniform expression of fgf8 throughout the entire embryo, all cells are exposed to the same level of Fgf signaling. Consequently, no local dorsalizing center is created and no partial secondary axis is generated. Furthermore, strong but relatively brief activation of the Fgf signaling pathway in the hsp:fgf8 transgenic line presumably reveals the immediate, direct consequences of ectopic Fgf signaling, whereas prolonged activation is known to affect dorsal ventral patterning, resulting in secondary effects.
Additional support for our interpretation is provided by the complementary expression patterns of Fgfs and foxi1. In zebrafish, fgf3, fgf8, fgf17b and fgf24 are all expressed in a dorsoventral gradient in the margin that later forms the germring of the gastrulating embryo, with highest levels on the dorsal side [39, 51, 54, 55]. In contrast, foxi1 and dlx3b are strongly expressed on the ventral side. Expression of the downstream targets of Fgf signaling, sprouty2 and sprouty4, is limited to the margin , indicating that Fgf signaling normally does not extend significantly into the ventral part of the embryo.
Our findings have profound consequences for the placement of foxi1 in the genetic pathway regulating otic development. Expression of foxi1 in the preotic region has been considered the earliest marker of otic induction [10, 56], but we show that foxi1 expression does not depend on Fgf signaling, the inducer of otic fate. Consistent with our previous model , we propose instead that Foxi1 (competence) and Fgf signaling (induction) represent two independent pathways that act in concert to activate pax8, which therefore is one of the earliest indicator of otic induction (Fig. 9).
Otic competence within the preplacodal region
Misexpression of fgf8 at the end of gastrulation leads to ectopic otic induction in a Foxi1 and Dlx3b dependent manner, but only within the preotic region. Treatment of wild-type embryos with RA, however, extends otic induction outside the normal preotic region to include the entire preplacodal domain that gives rise to all the cranial placodes. We show that most but not all of this ectopic otic induction is due to the misexpression of foxi1. Although misexpression of foxi1 promotes otic induction, the presence of Foxi1 and Dlx3b in non-neural cells alone is insufficient to initiate otic fate in response to Fgf signaling. During gastrulation, foxi1 and dlx3b are co-expressed in cells on the ventral side of the embryo, but we never observe pax8 expression in these cells even when Fgf is ectopically expressed in this region (data are not shown). However, at these stages the preplacodal domain, which represents the earliest stage of placode induction and which is required for otic induction [5, 7], has not yet been established. Strong ventral Bmp activity could be responsible for this limitation; a recent study suggests that attenuation of Bmp signaling is required for formation of the preplacodal region .
Our results show that not only fgf3 and fgf8 can act as otic inducers; we still detect some otic induction in fgf3, fgf8 double mutants treated with RA (Fig. 8). Candidates for this ectopic otic induction in the absence of fgf3 and fgf8 include fgf17a, fgf17b and fgf24 that are expressed at the anterior end of the embryo at bud stage [50, 51, 57].
Taken together our results reconcile the conflicting reports of ectopic otic induction after misexpression of Fgf. Irrespective of the species, a region abutting the hindbrain is competent to adopt the otic fate by the end of gastrulation and until early segmentation stages. In zebrafish, this region of competence is defined by Foxi1 and Dlx3b whereas in other species, the network upstream of Pax8 is still unknown. In chick, no Foxi1 genes have been reported and in mouse Foxi1 is expressed only very late during otic development, which might explain why disruption of Foxi1 causes only a mild otic phenotype without affecting early patterning or morphogenesis [58, 59]. Recent analysis of mouse Foxi class genes has revealed that Foxi2 and Foxi3 are expressed in the preotic region during otic induction ; thus these factors may provide otic competence in mouse similar to Foxi1 in zebrafish. At least one example of such a switch in function between orthologous genes in zebrafish and tetrapods has already been described  supporting the notion that a genetic network similar to what we have proposed for zebrafish  may regulate ear development in all vertebrates.
Embryos, obtained from the University of Oregon zebrafish facility, were produced using standard procedures  and were staged according to standard criteria  or by hours post fertilization at 28°C (h). The wild-type line used was AB. The mutant lines, acerebellarti282a, a strong hypomorphic allele of fgf8, snailhousety68a, a temperature-sensitive allele of bmp7, hearsay, a presumptive null allele of foxi1 and liat2414, a hypomorphic allele of fgf3, have been described previously [33, 64–66] and we refer to the homozygous mutants as fgf8, bmp7, foxi1 and fgf3, respectively. bmp7 embryos and their siblings were raised at 33°C .
To generate the hsp70:fgf8 construct, DNA fragments containing the zebrafish temperature-inducible hsp70 promoter  and the fgf8 gene  were cloned into the CS2+ vector . Preparation of the DNA construct for injection followed previous methods . Injected, putative founder fish (F0) were crossed inter se and their progeny (F1) were screened by PCR using hsp70 (5' CCC CGA CGA GGT GTT TAT TCG CTC 3') and fgf8 (5' CGG GGA CTG AAT GGT TAC CTG AGC 3') primers with the following PCR conditions: 3 minutes at 94°C; 35X (30 seconds at 94°C, 1 minute at 65°C, 1 minute at 72°C); 8 minutes at 72°C. For heat shock treatment, embryos still in their chorions were incubated in 37–39°C embryo medium in a 1.5 ml tube (20 embryos per tube) for 30 minutes in a heating block.
In situ hybridization, mRNA synthesis and microinjections
cDNA probes that detect the following genes were used: dlx3b ; erm ; fgf8 ; foxi ; otx1 ; otx2 ; pax8 ; pea3 ; stm ; vent ; cldna ; pax2a . Probe synthesis and single or double color in situ hybridization was performed essentially as previously described [75–77]. We purified the in vitro synthesized mRNA and probes using an RNeasy mini column (Qiagen GmbH). In vitro mRNA synthesis was performed using an SP6 RNA synthesis kit (Ambion). mRNAs were injected into all blastomeres of embryos at the 1-cell to 2-cell stage. RNA concentrations used for injections were: fgf8 (80 pg) and bmp2b (50 pg). Exogenous Bmp activity was provided by injection of mature, heterodimeric Bmp-2a (R&D Systems, 111-BM). At sphere stage (4 h), 6–8 μl of 200 ng/μl Bmp-2a (in PBS, 0.1% BSA, with phenol red added) was injected into the center of the blastoderm. More than 20 embryos were examined in each injection experiment.
Morpholinos (MOs) and pharmacological treatments
The dlx3b-MO, foxi1-MO vent-MO and vox-MO have been previously described [33, 34, 78]. For pharmacological treatments, the following stock solutions were made and stored at -80°C: 1 mM all-trans retinoic acid (RA; Sigma) in DMSO; 40 mM SU5402 (Calbiochem) in DMSO; 100 mg/ml cycloheximide (CHX; AG Scientific Inc., # 1189) in Ethanol. For embryo treatments, dilutions of these chemicals were made in embryo medium as follows: retinoic acid: 20 nM; SU5402: 40 μM; cycloheximide: 10-4M. Prior to gastrulation embryos were removed from their chorions and transferred into petri dishes containing the treatment solution, except for SU5402 treatments that were done in smaller volumes in glass vials. For control treatments, sibling embryos were incubated in corresponding dilutions of DMSO or Ethanol. CHX-treated embryos were fixed when control siblings reached 85–100% epiboly. All incubations were conducted in the dark.
Noden DM, van de Water TR: The developing ear: tissue orgins and interactions. The Biology of Change in Otolaryngology. Edited by: Ruben RJ,van de Water TR, Rubel EW. 1986, Amsterdam: Elsevier, 15-46.
Couly GF, Coltey PM, Le Douarin NM: The triple origin of skull in higher vertebrates: a study in quail-chick chimeras. Development. 1993, 117: 409-429.
Fritzsch BF, Barald KF, Lomax MI: Early embryology of the vertebrate ear. Development of the Auditory System. Edited by: Rubel EW, Popper AN, Fay RR. 1997, New York Springer Verlag, 80-145.
Barald KF, Kelley MW: From placode to polarization: New wrinkles in the development of the inner ear. Development. 2004, 131: 4119-30. 10.1242/dev.01339.
Streit A: Early development of the cranial sensory nervous system: from a common field to individual placodes. Dev Biol. 2004, 276: 1-15. 10.1016/j.ydbio.2004.08.037.
Litsiou A, Hanson S, Streit A: A balance of FGF, BMP and WNT signalling positions the future placode territory in thehead. Development. 2005, 132: 4051-62. 10.1242/dev.01964.
Martin K, Groves AK: Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otic placode induction. Development. 2006, 133: 877-87. 10.1242/dev.02267.
Torres M, Giráldez F: The development of the vertebrate inner ear. Mech Dev. 1998, 71: 5-21. 10.1016/S0925-4773(97)00155-X.
Whitfield TT, Riley BB, Chiang M-Y, Phillips B: Development of the zebrafish inner ear. Dev Dyn. 2002, 223: 427-458. 10.1002/dvdy.10073.
Brown ST, Martin K, Groves AK: Molecular basis of innerear induction. Curr Top Dev Biol. 2003, 57: 115-49.
Phillips BT, Bolding K, Riley BB: Zebrafish fgf3 and fgf8 encode redundant functions requiredfor otic placode induction. Dev Biol. 2001, 235: 351-365. 10.1006/dbio.2001.0297.
Maroon H, Walshe J, Mahmood R, Kiefer P, Dickson C, Mason I: Fgf3 and Fgf8 are required together for formation of the otic placode and vesicle. Development. 2002, 129: 2099-2108.
Léger S, Brand M: Fgf8 and Fgf3 are required for zebrafish ear placode induction, maintenance and inner ear patterning. Mech Dev. 2002, 119: 91-108. 10.1016/S0925-4773(02)00343-X.
Wright TJ, Mansour SL: Fgf3 and Fgf10 are required for mouse otic placode induction. Development. 2003, 130: 3379-3390. 10.1242/dev.00555.
Alvarez Y, Alonso MT, Vendrell V, Zelarayan LC, Chamero P, Theil T, Bösel MR, Shigeaki K, Maconochie M, Riethmacher D, Schimmang T: Requirements for FGF3 and FGF10 during inner ear formation. Development. 2003, 130: 6329-6338. 10.1242/dev.00881.
Ladher RK, Wright TJ, Moon AM, Mansour SL, Schoenwolf GC: FGF8 initiates inner ear induction in chick and mouse. Genes Dev. 2005, 19: 603-13. 10.1101/gad.1273605.
Mahmood R, Kiefer P, Guthrie S, Dickson C, Mason I: Multiple roles for FGF-3 during cranial neural development in the chicken. Development. 1995, 121: 1399-410.
Ladher RK, Anakwe KU, Gurney AL, Schoenwolf GC, Francis-West PH: Identification of synergistic signals initiating inner ear development. Science. 2000, 290: 1965-7. 10.1126/science.290.5498.1965.
Song J, Slack JM: Spatial and temporal expression of basic fibroblast growth factor (FGF-2) mRNA and protein in early Xenopus development. Mech Dev. 1994, 48: 141-51. 10.1016/0925-4773(94)90055-8.
Lombardo A, Isaacs HV, Slack JM: Expression and functions of FGF-3 in Xenopus development. Int J Dev Biol. 1998, 42: 1101-7.
Vendrell V, Carnicero E, Giraldez F, Alonso MT, Schimmang T: Induction of inner ear fate by FGF3. Development. 2000, 127: 2011-9.
Adamska M, Herbrand H, Adamski M, Kruger M, Braun T, Bober E: FGFs control the patterning of the inner ear but are not able to induce the full ear program. Mech Dev. 2001, 109 (2): 303-13. 10.1016/S0925-4773(01)00550-0.
Phillips BT, Storch MK, Lekven AC, Riley BB: A direct role for Fgf but not Wnt in otic placode induction. Development. 2004, 131: 923-931. 10.1242/dev.00978.
Solomon KS, Kwak SJ, Fritz A: Genetic interactions underlying otic placode induction and formation. Devel Dyn. 2004, 230: 419-433. 10.1002/dvdy.20067.
Bajoghli B, Aghaallaei N, Heimbucher T, Czer ny T: An artificial promoter construct for heat-inducible misexpression during fish embryogenesis. Dev Biol. 2004, 271: 416-30. 10.1016/j.ydbio.2004.04.006.
Baker CVH, Bronner-Frasier M: Vertebrate cranial placodes. I. Embryonic induction. Dev Biol. 2001, 232: 1-61. 10.1006/dbio.2001.0156.
Noramly S, Grainger RM: Determination of the embryonic inner ear. J Neurobiol. 2002, 53: 100-28. 10.1002/neu.10131.
Hans S, Liu D, Westerfield M: Pax8 and Pax2a function synergistically in otic specification, downstream of the Foxi1 and Dlx3b transcription factors. Development. 2004, 131: 5091-102. 10.1242/dev.01346.
Akimenko MA, Ekker M, Wegner J, Lin W, Westerfield M: Combinatorial expression of three zebrafish genes related to Distal-less : part of a homeobox code for the head. J Neurosi. 1994, 14: 3475-3486.
Ekker ME, Akimenko MA, BreMiller R, Westerfield M: Regional expression of three homeobox transcripts in the inner ear of zebrafish embryos. Neuron. 1992, 9: 27-35. 10.1016/0896-6273(92)90217-2.
Ellies D, Stock D, Hatch G, Giroux G, Weiss K, Ekker ME: Relationship between the genomic organization and the overlapping embryonic expression patterns of zebrafish dlx genes. Genomics. 1997, 45: 580-590. 10.1006/geno.1997.4978.
Kudoh T, Tsang M, Hukriede NA, Chen X, Dedekian M, Clarke CJ, Kiang A, Schultz S, Epstein JA, Toyama R, Dawid IB: A gene expression screen in zebrafish embryogenesis. Genome Res. 2001, 11: 1979-87. 10.1101/gr.209601.
Solomon KS, Fritz A: Concerted action of two dlx paralogs in sensory placode formation. Development. 2002, 129: 3127-3136.
Liu D, Chu H, Maves L, Yan YL, Morcos PA, Postlethwait P, Westerfield M: Fgf3 and Fgf8 dependent and independent transcription factors are required for otic placode specification. Development. 2003, 130: 2213-2224. 10.1242/dev.00445.
Thisse B, Fauny JD, Hamadbachir A, Thisse C: High Throughput Expression Analysis of ZF-Models Consortium Clones. 2005, ZFIN Direct Data Submission.
Solomon KS, Kudoh T, Dawid IG, Fritz A: Zebrafish foxil mediates otic placode formation and jaw development. Development. 2003, 130: 929-940. 10.1242/dev.00308.
Nissen RM, Yan J, Amsterdam A, Hopkins N, Burgess SM: Zebrafish foxi one modulates cellular responses to Fgf signaling required for the integrity of ear and jaw. Development. 2003, 130: 2543-2554. 10.1242/dev.00455.
Nguyen VH, Schmid B, Trout J, Conners SA, Ekker M, Mullins MC: Ventral and lateral regions of the zebrafish gastrula, including the neural crest progenitors, are established by a bmp2b/swirl pathway of genes. Dev Biol. 1998, 199: 93-110. 10.1006/dbio.1998.8927.
Fürthauer M, Van Celst J, Thisse C, Thisse B: Fgf signalling controls the dorsoventral patterning of the zebrafish embryo. Development. 2004, 131: 2853-64. 10.1242/dev.01156.
Kudoh T, Concha ML, Houart C, Dawid IB, Wilson SW: Combinatorial Fgf and Bmp signalling patterns the gastrula ectoderm into prospective neural and epidermal domains. Development. 2004, 131: 3581-92. 10.1242/dev.01227.
Rentzsch F, Bakkers J, Kramer C, Hammerschmidt M: Fgf signaling induces posterior neuroectoderm independently of Bmp signaling inhibition. Dev Dyn. 2004, 231: 750-7. 10.1002/dvdy.20244.
Massague' J: Integration of Smad and MAPK pathways a link and a linker revisited. Genes Dev. 2004, 17: 2993-2997. 10.1101/gad.1167003.
Pera EM, Ikeda A, Eivers E, De Robertis EM: Integration of IGF, FGF, and anti-BMP signals via Smad1 phosphorylation in neural induction. Genes Dev. 2004, 17: 3023-3028. 10.1101/gad.1153603.
Mohammadi M, McMahon G, Sun L, Tang C, Hirth P, Yeh BK, Hubbard SR, Schlessinger J: Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science. 1997, 276: 955-60. 10.1126/science.276.5314.955.
Kawahara A, Wilm T, Solnica-Krezel L, Dawid IB: Functional interaction of vega2 and goosecoid homeobox genes in zebrafish. Genesis. 2000, 28: 58-67. 10.1002/1526-968X(200010)28:2<58::AID-GENE30>3.0.CO;2-N.
Melby AE, Beach C, Mullins M, Kimelman D: Patterning the early zebrafish by the opposing actions of bozozok and vox/vent. Dev Biol. 2000, 224: 275-85. 10.1006/dbio.2000.9780.
Roehl H, Nüsslein-Volhard C: Zebrafish pea3 and erm are general targets of FGF8 signaling. Curr Biol. 2001, 11: 503-7. 10.1016/S0960-9822(01)00143-9.
Raible F, Brand M: Tight transcriptional control of the ETS domain factors Erm and Pea3 by Fgf signaling during early zebrafish development. Mech Dev. 2001, 107: 105-17. 10.1016/S0925-4773(01)00456-7.
Fischer S, Draper BW, Neumann CJ: The zebrafish fgf24 mutant identifies an additional level of Fgf signaling involved in vertebrate forelimb initiation. Development. 2003, 130: 3515-24. 10.1242/dev.00537.
Reifers F, Adams J, Mason IJ, Schulte-Merker S, Brand M: Overlapping and distinct functions provided by fgf17, a new zebrafish member of the Fgf8/17/18 subgroup of Fgfs. Mech Dev. 2000, 99: 39-49. 10.1016/S0925-4773(00)00475-5.
Cao Y, Zhao J, Sun Z, Zhao Z, Postlethwait J, Meng A: fgf17b, a novel member of Fgf family, helps patterning zebrafish embryos. Dev Biol. 2004, 271: 130-43. 10.1016/j.ydbio.2004.03.032.
Thisse B, Pflumio S, Fürthauer M, Loppin B, Heyer V, Degrave A, Woehl R, Lux A, Steffan T, Charbonnier XQ, Thisse C: Expression of the zebrafish genome during embryogenesis. 2000, ZFIN Direct Data Submission
Westerfield M, Wegner J, Jegalian BG, DeRobertis EM, Puschel AW: Specific activation of mammalian Hox promoters in mosaic transgenic zebrafish. Genes Dev. 1992, 6: 591-8.
Fürthauer M, Thisse C, Thisse B: A role for FGF-8 in the dorsoventral patterning of the zebrafish gastrula. Development. 1997, 124: 4253-64.
Reifers F, Bohli H, Walsh EC, Crossley PH, Stainier DYR: Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary and somitogenesis. Development. 1998, 125: 2381-2395.
Riley BB: Genes controlling the development of the zebrafish inner ear and hair cells. Curr Top Dev Biol. 2003, 57: 357-88.
Draper BW, Stock DW, Kimmel CB: Zebrafish fgf24 functions with fgf8 to promote posterior mesodermal development. Development. 2003, 130: 4639-54. 10.1242/dev.00671.
Hulander M, Wurst w, Carlsson P, Ernerbäck S: The winged helix transcription factor Fkh10 is required for normal development of the inner ear. Nat Genet. 1998, 20: 374-376. 10.1038/3850.
Hulander M, Kiernan AE, Blomqvist SR, Carlsson P, Samuelsson EJ, Johansson BR, Steel KP, Enerbäck S: Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxil null mutant mice. Development. 2003, 130: 2013-2025. 10.1242/dev.00376.
Ohyama T, Groves AK: Expression of mouse Foxi class genes in early craniofacial development. Dev Dyn. 2004, 231: 640-6. 10.1002/dvdy.20160.
Rhinn M, Lun K, Amores A, Yan YL, Postlethwait JH, Brand M: Cloning, expression and relationship of zebrafish gbx1 and gbx2 genes to Fgf signaling. Mech Dev. 2003, 120: 919-36. 10.1016/S0925-4773(03)00135-7.
Westerfield M: The zebrafish book. A guide for the laboratory use of zebrafish (Danio rerio). 2000, Eugene: Univ. of Oregon Press
Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF: Stages of embryonic development of the zebrafish. Dev Dyn. 1995, 203: 253-310.
Brand M, Heisenberg CP, Jiang YJ, Beuchle D, Lun K, Furutani-Seiki M, Granato M, Haffter P, Hammerschmidt M, Kane D, et al: Mutations in zebrafish affecting the formation of the boundary between midbrain and hindbrain. Development. 1996, 123: 179-190.
Dick A, Hild M, Bauer H, Imai Y, Maifeld H, Schier AF, Talbot WS, Bouwmeester T, Hammerschmidt M: Essential role of Bmp7 (snailhouse) and its prodomain in dorsoventral patterning of the zebrafish embryo. Development. 2000, 127: 343-54.
Herzog W, Sonntag C, von der Hardt S, Roehl HH, Varga ZM, Hammerschmidt M: Fgf3 signaling from the ventral diencephalon is required for early specification and subsequent survival of the zebrafish adenohypophysis. Development. 2004, 131: 3681-92. 10.1242/dev.01235.
Halloran MC, Sato-Maeda M, Warren JT, Su F, Lele Z, Krone PH, Kuwada JY, Shoji W: Laser-induced gene expression in specific cells of transgenic zebrafish. Development. 2000, 127: 1953-60.
Turner DL, Weintraub H: Expression of achaete-scute homologue 3 in Xenopus embryos converts ectodermal cells to a neural fate. Genes Dev. 1994, 8: 1434-1447.
Scheer N, Campos-Ortega JA: Use of the Gal4-UAS technique for targeted gene expression in the zebrafish. Mech Dev. 1999, 80: 153-8. 10.1016/S0925-4773(98)00209-3.
Li Y, Allende ML, Finkelstein R, Weinberg ES: Expression of two zebrafish orthodenticle-related genes in the embryonic brain. Mech Dev. 1994, 48: 229-44. 10.1016/0925-4773(94)90062-0.
Pfeffer PL, Gerster T, Lun K, Brand M, Busslinger M: Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 on the Pax2.1 (noi) function. Development. 1998, 125: 3063-3074.
Söllner C, Burghammer M, Busch-Nentwich E, Berger J, Schwarz H, Riekel C, Nicolson T: Control of crystal size and lattice formation by starmaker in otolith biomineralization. Science. 2003, 302: 282-6. 10.1126/science.1088443.
Kollmar R, Nakamura SK, Kappler JA, Hudspeth AJ: Expression and phylogeny of claudins in vertebrate primordia. Proc Natl Acad Sci USA. 2001, 98: 10196-10201. 10.1073/pnas.171325898.
Krauss S, Johansen T, Korzh V, Fjose A: Expression of the zebrafish paired box gene pax [zf-b] during early neurogenesis. Development. 1991, 113: 1193-1206.
Thisse C, Thisse B, Schilling T, Postlethwait JH: Structure of the zebrafish snail gene and its expression in wild-type, spadetail and no tail mutant embryos. Development. 1993, 119: 1203-1215.
Jowett T, Yan YL: Double fluorescent in situ hybridization to zebrafish embryos. Trends Genet. 1996, 12: 387-9. 10.1016/S0168-9525(96)90091-8.
Whitlock KE, Westerfield M: The olfactory placodes of the zebrafish form by convergence of cellular fields at the edge of the neural plate. Development. 2000, 127: 3645-3653.
Imai Y, Gates MA, Melby AE, Kimelman D, Schier AF, Talbot WS: The homeobox genes vox and vent are redundant repressors of dorsal fates in zebrafish. Development. 2001, 128: 2407-20.
We wish to thank Sandra Brown and Lauren Clancey for technical assistance; John Kuwada for providing the hsp70 promoter; Wiebke Herzog for the fgf3 mutants; Michael Brand for critical reading of the manuscript; Marie-Christine Ramel for her cycloheximide protocol. This work was supported by NIH grants DC04186 and HD22486. S.H. is a recipient of a Feodor Lynen fellowship of the Alexander von Humboldt foundation; D.L. was supported by a postdoctoral fellowship of the Canadian Institutes of Health Research.
SH conceived the study, carried out most of the experiments, analyzed the data and drafted the manuscript. JC contributed design and execution of the Bmp2a protein overexpression and cycloheximide experiments, and helped draft the manuscript. DL contributed to the design of the experiments and helped to draft the manuscript. MW, contributed to design and coordination of the experiments, and helped draft the manuscript. All authors have read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Heat shock at the end of gastrulation produces strong and ubiquitous fgf8 expression in transgenic animals. (A-C, G-K) Following a 30 minute heat shock, strong and ubiquitous expression of fgf8 can be observed in the transgenic embryos (G-K) up to 1.5 hours after heat shock, masking the endogenous fgf8 expression domains that are observed in the wild-type embryos (A-C). (D, I) Ectopic fgf8 mRNA is gradually lost and the endogenous fgf8 expression domains emerge at 2 hours after heat shock. (D, I) At 2.5 hours after heat shock only scattered cells show ectopic fgf8 expression in transgenic embryos. Dorsal views of 2–5-somite stage embryos with anterior towards the top. h, hours after heat shock; mhb, midbrain-hindbrain border; tb, tail bud. Scale bar: 100 μm. (JPEG 72 KB)
Additional file 2: Retinoic acid treatment has little effect on patterning along the anterior-posterior axis. (A, B, D, E) Expression of fgf3 or fgf8 in embryos treated with 20 nM RA is indistinguishable from control embryos treated with DMSO. (C, F) In RA treated embryos expression of sox9a in the preotic region expands to surround the anterior neural plate border in comparison to control embryos. However, sox9a expression in the hindbrain is identical in RA and DMSO treated embryos. Dorsal views of 1–5-somite stage embryos with anterior towards the top. fb, forebrain; hb, hindbrain; hp, heart primordium; mhb, midbrain-hindbrain border; r4, rhombomere 4; po, preotic region. Scale bar: 40 μm μm. (JPEG 112 KB)
Additional file 3: The increase in otic tissue, following a heat shock at late gastrulation stages of transgenic hsp:fgf8 embryos, is transient. (A, D) At 28 hours post fertilization, otic vesicles in transgenic fish heat shocked at late gastrulation stages are still larger than in non-transgenic siblings. (B, C, E, F) The size difference of otic vesicles in transgenic and non-transgenic embryos is less prominent at 50 hours post fertilization, and indistinguishable by 72 hours post fertilization. Lateral views of live otic vesicles with anterior to the left and dorsal towards the top. o, otolith. Scale bar: 120 μm. (JPEG 107 KB)
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Hans, S., Christison, J., Liu, D. et al. Fgf-dependent otic induction requires competence provided by Foxi1 and Dlx3b. BMC Dev Biol 7, 5 (2007). https://doi.org/10.1186/1471-213X-7-5