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Zebrafish Mnx proteins specify one motoneuron subtype and suppress acquisition of interneuron characteristics

Abstract

Background

Precise matching between motoneuron subtypes and the muscles they innervate is a prerequisite for normal behavior. Motoneuron subtype identity is specified by the combination of transcription factors expressed by the cell during its differentiation. Here we investigate the roles of Mnx family transcription factors in specifying the subtypes of individually identified zebrafish primary motoneurons.

Results

Zebrafish has three Mnx family members. We show that each of them has a distinct and temporally dynamic expression pattern in each primary motoneuron subtype. We also show that two Mnx family members are expressed in identified VeLD interneurons derived from the same progenitor domain that generates primary motoneurons. Surprisingly, we found that Mnx proteins appear unnecessary for differentiation of VeLD interneurons or the CaP motoneuron subtype. Mnx proteins are, however, required for differentiation of the MiP motoneuron subtype. We previously showed that MiPs require two temporally-distinct phases of Islet1 expression for normal development. Here we show that in the absence of Mnx proteins, the later phase of Islet1 expression is initiated but not sustained, and MiPs become hybrids that co-express morphological and molecular features of motoneurons and V2a interneurons. Unexpectedly, these hybrid MiPs often extend CaP-like axons, and some MiPs appear to be entirely transformed to a CaP morphology.

Conclusions

Our results suggest that Mnx proteins promote MiP subtype identity by suppressing both interneuron development and CaP axon pathfinding. This is, to our knowledge, the first report of transcription factors that act to distinguish CaP and MiP subtype identities. Our results also suggest that MiP motoneurons are more similar to V2 interneurons than are CaP motoneurons.

Background

The ability of an animal to carry out behavior depends on precise innervation of each muscle by the appropriate motoneuron subtype. Motoneuron subtype identity is specified by the combination of transcription factors expressed by a cell during its differentiation, and recognized by characteristic features, such as soma position, axon trajectory and muscle innervation pattern. Although specification of motoneuron subtype identity has been well-studied[1, 2], we still have an incomplete picture of the molecular mechanisms regulating this process. Here we take advantage of the ability to recognize individual primary motoneurons (PMNs) in the spinal cord of embryonic zebrafish to explore the roles of Mnx family transcription factors in motoneuron subtype specification.

Spinal cord neurons develop from distinct progenitor domains defined by expression of specific transcription factors[2, 3]. Zebrafish PMNs are derived from the progenitor of motoneuron (pMN) domain[4] and comprise three subtypes: CaP, MiP and RoP, each of which can be distinguished based on soma position, axon trajectory and muscle innervation[5]. A fourth PMN, VaP, is variably present, initially equivalent to CaP, and later typically dies[6, 7]. Here we focus on CaP, which innervates ventral myotome and MiP, which innervates dorsal myotome. Initially both CaP and MiP express Islet1, a transcription factor required for PMN development. In the absence of Islet1, PMNs develop axon trajectories and express the neurotransmitter characteristic of VeLD interneurons[8], which are also derived from the pMN domain[4]. Later in development, CaP down-regulates Islet1 and expresses a related protein, Islet2a. MiP also down-regulates Islet1, but then re-expresses it about an hour later[9, 10]. The second phase of Islet1 expression is regulated by Nkx6 transcription factors. In the absence of Nkx6 proteins, MiP axon formation begins normally with the extension of a ventral axon to the muscle pioneers, an identified set of muscle fibers that separate dorsal and ventral muscle[11]. However, MiP then fails to extend its normal axon collateral to dorsal muscle, and instead develops an interneuron-like axon within the spinal cord[10]. This interneuron-like axon often resembles axons of V2a interneurons[12, 13] that are derived from the p2 domain situated just dorsal to the pMN domain[3]. The p2 domain, which generates excitatory V2a and inhibitory V2b neurons, has been shown to be closely related to the pMN domain based on shared expression of a number of transcription factors[2].

The vertebrate Mnx family comprises homeodomain transcription factors originally isolated in human and subsequently isolated in chick and mouse[14]. Mnx2 (previously called MNR2 and Hlxb9l[14]) was isolated from a single chick cell induced to become a motoneuron[15]. Mnx2 is expressed in motoneuron progenitors and in post-mitotic motoneurons. Ectopic expression of Mnx2 is sufficient to induce motoneuron differentiation in Islet1-positive spinal cord neurons; whether Mnx2 is necessary for motoneuron differentiation has not been tested. Mnx1 (previously called Hb9 and Hlxb9[14]) was isolated in mice and shown to be necessary for normal differentiation of many motoneurons[16, 17]. In its absence, motoneurons still project axons to the periphery, but the axon projections are abnormal and the cells inappropriately express a marker of V2a interneurons[18]. In both chick and mouse, Mnx proteins are exclusive to motoneurons at early stages of spinal cord development[1517]; however, later in development Mnx1 is expressed in a small set of interneurons[19].

We provide evidence for a novel role of Mnx proteins in zebrafish motoneuron subtype specification. Zebrafish have three Mnx proteins, Mnx1 and two co-orthologs of Mnx2, Mnx2a and Mnx2b[20], all of which are expressed primarily in post-mitotic neurons. We show that each Mnx family member is expressed in a distinct pattern in each PMN subtype, and that this pattern is dynamic during PMN differentiation. In contrast to early developmental stages in chicks and mice when Mnx expression within the spinal cord is exclusive to motoneurons[1517], two zebrafish Mnx family members are expressed in VeLD interneurons. We used morpholino antisense oligonucleotides (MOs[21]) to knock down Mnx function and found, to our surprise, that CaPs and VeLDs developed normally. In contrast, Mnx proteins are required for normal MiP development. In their absence, the second phase of MiP Islet1 expression is initiated at the appropriate time, but is lost a few hours later. MiPs in mnx MO-injected embryos express markers of V2a interneurons, similar to what has been reported in mouse mutants[16, 17]. However, in contrast to mouse mutants, these MiPs also developed V2a-like axons in addition to peripheral axons projecting to muscle. Surprisingly, the peripheral axons of these MiPs did not extend to their normal dorsal muscle targets, but instead projected ventrally alongside normal CaP axons. In some cases, MiPs appeared to be entirely transformed to a CaP morphology in the absence of Mnx proteins. These studies identify Mnx proteins as essential in preventing MiPs from expressing characteristics of V2a interneurons. They also reveal an unexpected role for Mnx proteins in specifying MiP subtype identity by preventing MiPs from developing as CaPs.

Results

mnx family genes are dynamically expressed in primary motoneurons and VeLD interneurons

We characterized expression of mnx1, mnx2a and mnx2b within the zebrafish spinal cord using RNA in situ hybridization. To determine the specific PMNs that express each mnx gene, we simultaneously labeled islet1 mRNA, which is initially expressed in all PMNs[9] and each of the mnx family members. At later stages we included either islet1, which is expressed in RoP and MiP, or islet2a, which is expressed in CaP and VaP[9]. After 20 hpf, islet1 and islet2a are also expressed by smaller, more ventrally-located secondary motoneurons[9, 22, 23] that we excluded from our analyses.

Each mnx gene has a dynamic and specific expression pattern in each of the PMNs. mnx1 was expressed in all four PMNs from 14 to 24 hpf (Figure1A-D). In contrast, mnx2a was initially expressed in only CaP and VaP from 14 to 18 hpf (Figure1E, F). However, by 20 hpf, mnx2a expression has expanded to all four PMNs, a pattern that persisted through 24 hpf (Figure1G, H). mnx2b was initially expressed in all four PMNs from 14 to 18 hpf (Figure1I, J). Intriguingly, by 20 hpf, mnx2b expression was reduced to a single islet1+ PMN (Figure1K, L). To learn which PMN expressed mnx2b after 20 hpf, we injected UAS:GFP plasmid into Tg(mnx1:GAL4) embryos, which resulted in mosaic expression of GFP and thus revealed both the soma and axon trajectory of GFP-positive neurons. We then processed the embryos at 28 hpf for GFP and Mnx2b immunohistochemistry. Based on its expression of islet1 at 24 hpf (Figure1K) and dorsal axon, the Mnx2b+ PMN is MiP (Figure1M).

Figure 1
figure 1

Zebrafish mnx family genes are dynamically expressed in PMNs and VeLD interneurons. Lateral views, anterior to the left; all figures are in this orientation unless otherwise noted. MiPs and RoPs are outlined green in panels with islet1 labeling, CaPs and VaPs are outlined blue in panels with islet2a labeling. Segment boundaries are demarcated with diagonal lines. (A-L) RNA expression; two spinal hemisegments are shown in each panel. At 14 hpf, mnx1 is co-expressed with both islet1 (A) and islet2a (B), mnx2a is only co-expressed with islet2a (E, F), and mnx2b is co-expressed with both islet1 (I) and islet2a (J). The VeLD interneuron can be seen expressing both mnx1 (arrowheads A, B) and mnx2b (arrowheads I, J). At 24 hpf, mnx1 maintains co-expression with both islet1 (C) and islet2a (D), mnx2a is co-expressed with both islet1 (G) and islet2a (H), and mnx2b is co-expressed only with islet1 (K, L). VeLD still expresses mnx1 (arrowhead C). (M-N) Protein expression. Mnx2b protein (red) co-localizes with the MiP soma (GFP; green) (M). Mnx1 protein (red) co-localizes with the VeLD soma (GFP; green) (N). (O) Schematic of mnx expression. Scale bar: 10 μm, A-L; 10 μmm M; 20 μm N.

In addition to expression in PMNs, mnx1 and mnx2b are also expressed in a slightly more dorsal cell first visible at about 14 hpf (Figure1A, I). mnx1 expression persisted in this cell through 24 hpf, but mnx2b expression was extinguished around 20 hpf. The position and early appearance of these mnx1+mnx2b+ cells suggested that they were VeLD interneurons, which can be uniquely identified based on their lateral position, soma shape, and axon trajectory[4, 2426]. To test this, we labeled VeLDs by injecting the UAS:GFP plasmid into Tg(mnx1:GAL4) embryos and verified that they expressed Mnx1 by immunohistochemistry (Figure1N). We also showed that mnx1 is co-expressed with the VeLD marker gad (glutamic acid decarboxylase, an enzyme in the synthetic pathway for the neurotransmitter GABA;[8, 2729]), but not with vglut (vesicular glutamate transporter), a marker of excitatory, glutamatergic V2a interneurons[12] (Additional file1: Figure S1).

To explore the possibility that mnx genes are expressed by other interneurons with descending axons we looked for co-expression of mnx1 and vsx2 or gata3, markers of V2a and V2b fate, respectively[13, 29]. Expression of mnx1 and these markers was always mutually exclusive (Additional file1: Figure S1 and data not shown), ruling out expression of mnx family genes in V2a and V2b interneurons. Based on its descending axon, early appearance and gad expression, the interneuron positive for expression of both mnx1 and mnx2b is VeLD.

In mice and chicks, members of the mnx gene family are expressed in motoneuron progenitors prior to exit from the cell cycle. In zebrafish, PMNs and VeLDs adjacent to somites 5 to 15 emerge from olig2:GFP+ progenitors in the pMN domain[4], exit the cell cycle between 9 and 16 hpf[30], and then down-regulate olig2[31], although GFP persists for a short time. To determine if zebrafish Mnx proteins are expressed in PMN progenitors, we examined expression in Tg(olig2:GFP) embryos (Additional file2: Figure S2). We found Mnx1+ cells that were either GFP- or expressed low levels of GFP; these cells often co-expressed Elavl3, a marker of post-mitotic neurons but did not co-express phosphohistone H3 (PH3), a marker of mitotic cells. Similarly, Mnx2a was often co-expressed with Elavl3 and never co-expressed with PH3, even though Mnx2a was expressed in some cells with high levels of GFP. Although mnx2b RNA was present as early as 14 hpf, we could not detect Mnx2b protein until at least 20 hpf, and then it was present only in MiPs (Figure1O). Together these data are most consistent with the idea that all three Mnx proteins are first expressed in post-mitotic neurons and that expression of Mnx2a precedes expression of Mnx1.

In addition to examining Mnx expression in early-developing PMNs and VeLD interneurons, we also characterized Mnx expression in later-developing secondary motoneurons (SMNs). By 26 hpf, Mnx1 is expressed in a subset of mostly dorsally-located SMNs (Additional file3: Figure S3), Mnx2a is expressed in a subset of mostly ventrally-located SMNs (Additional file3: Figure S3), and Mnx2b is rarely expressed in SMNs (data not shown).

mnx expression is independent of Islet1

Islet1 and Lhx3 cooperate to regulate Mnx1 expression in chicks[32, 33]. To learn whether this relationship is conserved in zebrafish, we injected MOs to knock down either Islet1[8], or Lhx3 and Lhx4 (Hutchinson SA, Seredick S, Van Ryswyk L, Talbot JC, Eisen JS: Lhx3 and Lhx4 regulate interneuron fate and prevent motoneurons from co-expressing interneuron characteristics, unpublished), and examined mnx gene expression. Surprisingly, expression of all three mnx genes was unaffected by Islet1 knockdown (Additional file4: Figure S4). Moreover, at 24 hpf only mnx2b expression was eliminated in the absence of Lhx3 and Lhx4, revealing that Islet1 and Lhx3 do not cooperate to regulate mnx expression in zebrafish (Additional file4: Figure S4).

Overexpression of Mnx proteins in chicks induces formation of ectopic motoneurons expressing Islet, Lhx3 and other Mnx paralogs[15, 34]. To test the hypothesis that Mnx proteins regulate expression of lhx genes in zebrafish, we injected mnx MOs and examined expression of lhx3 and lhx4. We found that neither lhx3 nor lhx4 expression was affected by the absence of Mnx proteins. We also eliminated expression of Mnx1, Mnx2a and Mnx2b individually and examined expression of each mnx gene. In the absence of any one mnx gene, expression of other paralogs was unaffected, revealing that each member of the gene family is regulated independently of the others (Additional file4: Figure S4).

Mnx proteins are unnecessary for formation of primary motoneurons and VeLD interneurons

To test the function of Mnx proteins in PMN development we used previously validated translation-blocking morpholinos[20] (Additional file5: Figure S5). To determine whether PMNs form in the absence of Mnx proteins, we assessed three markers of PMN identity: Islet[8], chat, which encodes an enzyme required to synthesize acetylcholine[35] and nrp1a:GFP, a transgene expressed in CaP and VaP before 18 hpf[36] and in all PMNs at later stages. All three markers were expressed normally in the combined absence of Mnx1, Mnx2a, and Mnx2b (Figure2A-D), indicating that PMN specification is normal.

Figure 2
figure 2

Mnx proteins are not required for formation of PMNs or VeLDs. Control and mnx MO-injected embryos labeled with markers of PMN or VeLD identity. (A-B) At 16 hpf, PMNs express chat and nrp1a:GFP in control (A) and mnx MO-injected embryos (B). (C-D) At 18 hpf, PMNs express Islet in control (C) and mnx MO-injected Tg(nrp1a:GFP) embryos (D). (E-F) At 20 hpf, VeLD interneuron (arrowheads) numbers and distribution are the same in control (E) and mnx MO-injected Tg(vsx1:GFP) embryos (F); n = 80 segments in 10 embryos for control and mnx MO-injected samples. Scale bar: 15 μm, A-B; 20 μm, C-F.

To assess whether VeLD development was compromised in the absence of Mnx proteins, we examined expression of Gad65/67, the biosynthetic enzyme for GABA, in Tg(vsx1:GFP) embryos. VeLDs express Gad65/67 but not vsx1:GFP, and can be uniquely identified by their lateral position and soma shape. At 20 hpf, the number of VeLDs in the absence of all three Mnx proteins was indistinguishable from controls (Figure2E, F). Moreover, at 28 hpf VeLDs were morphologically normal in the absence of Mnx proteins (data not shown). Together these data provide evidence that Mnx proteins are not required for VeLD or PMN generation, and that both cell types acquire aspects of their mature identity in the absence of Mnx proteins.

Mnx proteins promote formation of normal MiP axons

Because mnx genes are expressed during and after the period of PMN subtype commitment[25], we examined whether Mnx proteins play a role in subtype specification. Normally all PMNs express islet1 as they exit the cell cycle and then later express only one islet gene characteristic of their subtype: MiP and RoP express islet1, whereas CaP and VaP express islet2a[9]. In the absence of all three Mnx proteins, CaPs inappropriately expressed both islet1 and islet2a (Figure3A, B). However, these cells formed normal, ventrally-extending CaP axons and appeared morphologically indistinguishable from CaPs in control embryos (Figure3C, D), consistent with our previous finding that islet1 and islet2a can play equivalent roles in CaP specification[8].

Figure 3
figure 3

Mnx proteins promote MiP subtype identity and prevent interneuron-like and CaP-like processes. (A-D) Control and mnx MO-injected embryos. (A) In controls islet1 and islet2a expression is mutually exclusive at 18 hpf. (B) In embryos injected with mnx1, mnx2a, and mnx2b MOs, islet1 is co-expressed with islet2a in CaP and VaP. (C) Control embryos have normal, ventrally-projecting CaP axons (arrows) and dorsally-projecting MiP axons (arrowheads). (D) CaP axons (arrows) are normal in mnx MO-injected embryos whereas MiP axons (closed arrowheads) are absent and there are ectopic interneuron-like axons (open arrowheads). (E-J′′) Rhodamine-dextran-labeled MiPs in 28 to 32 hpf Tg(nrp1a:GFP) embryos injected with mnx1, mnx2a, and mnx2b MOs. Panels show rhodamine-dextran labeling (no superscript), nrp1a:GFP () and a merged image of the two channels (′′). Labeled MiPs (yellow arrowheads) become hybrids with six morphologies. (E-E′′) V2a hybrids express nrp1a:GFP and have a descending V2a-like axon. (F-F′′) MiP-V2a hybrids have a descending V2a-like axon as well as a normal-appearing MiP ventral axon; the red blob to the right is a cell that was killed during labeling. (G-G′′) MiP-V2a-CaP hybrids have a descending V2a-like axon as well as a ventrally-projecting CaP-like axon. (H-H′′) MiP-CaP hybrids have both a normal MiP axon and a CaP-like axon. (I-I′′) Truncated MiP-CaP hybrids have a truncated MiP dorsal axon as well as a ventrally-projecting CaP-like axon. (J-J′′) CaP hybrids have a CaP-like axon that extends next to a normal CaP axon. Scale bar: 20 μm, A-D; 40 μm, E-H′′.

Strikingly, MiP dorsal axons were almost entirely absent from embryos lacking all three Mnx proteins (Figure3C, D; Table1). To determine if a subset of the Mnx proteins is responsible for the MiP axon phenotype, we knocked down each Mnx protein singly or in pairs and counted the number of MiP axons in the mid-trunk. We saw no phenotype in the absence of any single Mnx protein, or in the absence of Mnx1 plus Mnx2a, or Mnx1 plus Mnx2b. However, in the absence of both Mnx2a and Mnx2b, MiP axons were absent from nearly half the segments, and when present they were often truncated (Table1). Thus, the two Mnx2 paralogs appear to play a predominant role in formation of normal, dorsally-projecting MiP axons, although the increased severity of the triple Mnx protein knockdown demonstrates that all three Mnx proteins are involved in this process.

Table 1 Mnx proteins are required for MiP formation

The absence of normal MiP dorsal axons from mnx MO-injected embryos led us to consider whether MiPs developed abnormal axon projections. Consistent with this idea, nrp1a:GFP+ descending interneuron axons were present in the ventral spinal cords of embryos lacking all three Mnx proteins, something never seen in control embryos (Figure3C, D). To examine the morphology of MiPs in triple mnx MO-injected Tg(nrp1a:GFP) embryos in more detail, we labeled individual GFP-expressing cells in the MiP position with rhodamine-dextran. During these experiments, we noted that unlike CaPs, which express GFP very brightly in triple mnx MO-injected Tg(nrp1a:GFP) embryos, MiPs were difficult to detect because they expressed GFP dimly, if at all. When we scored GFP+, rhodamine-labeled MiPs, we observed a range of phenotypes. In some cases we labeled GFP+ cells that had only a V2a interneuron-like axon that descended many segments within the spinal cord (V2a hybrid; Figure3E-E”; Figure4). Some MiPs initiated motoneuron development by projecting a normal-appearing ventral axon that stopped at the muscle pioneers. Instead of also projecting a collateral to dorsal muscle, however, these cells developed a V2a interneuron-like axon (MiP-V2a hybrid; Figure3F-F”; Figure4). Surprisingly, in some cases the ventral axons of labeled MiPs failed to stop at the muscle pioneers, instead extending as far ventrally as CaP axons (MiP-V2a-CaP hybrid; Figure3G-G”; Figure4). In other cases, labeled cells had both a normal MiP axon and a CaP-like axon (MiP-CaP hybrid; Figure3H-H”; Figure4), or had both a truncated MiP axon and a CaP-like axon (truncated MiP-CaP hybrid; Figure3I-I”; Figure4). We also labeled MiPs that had only a CaP-like axon (CaP hybrid; Figure J-J”; Figure4), suggesting that some MiPs entirely transformed to a CaP morphology. Based on these observations, we conclude that Mnx proteins are required both to prevent MiPs from developing V2a interneuron-like axons and to prevent MiPs from extending a ventral axon along the pathway normally followed by the CaP axon.

Figure 4
figure 4

Mnx proteins prevent MiPs from acquiring inappropriate axonal projections. In the absence of Mnx proteins, MiPs adopt one of 6 alternative hybrid axonal projections. The number of labeled MiPs we observed in each category is indicated below the diagram of each alternative hybrid.

Mnx proteins prevent MiPs from acquiring molecular characteristics of V2a interneurons

To ascertain whether MiPs in mnx-deficient embryos take on molecular as well as morphological characteristics of V2a interneurons, we assayed for co-expression of interneuron and motoneuron markers. We found that in triple mnx MO-injected embryos, MiPs co-expressed cholinergic and glutamatergic markers (Figure5A, B). This phenotype was never seen in MiPs or CaPs in control embryos or in CaPs in mnx MO-injected embryos. This hybrid neurotransmitter phenotype is specific, as expression of cholinergic and GABAergic or glycinergic markers was always mutually exclusive in both controls and MO-injected embryos (Additional file6: Figure S6).

Figure 5
figure 5

Mnx proteins prevent MiPs from acquiring V2a-like molecular characteristics. (A-D) Single spinal hemisegments of control and mnx MO-injected embryos. MiPs (closed arrowheads) and CaPs (open arrowheads) are indicated in merged panels (right column). (A) In control embryos, MiPs and CaPs express chat but never vglut (0/20 vglut+ MiPs or CaPs in five embryos). (B) In mnx MO-injected embryos, MiPs co-express both chat and vglut (22/41 vglut+ MiPs in eight embryos), while CaPs express chat but not vglut (0/41 vglut+ CaPs in eight embryos. (C) In control embryos, MiPs express islet1 but not vsx2 (0/50 vsx2+ MiPs in 10 embryos), while CaPs express neither islet1 nor vsx2 (0/50 vsx2+ CaPs in 10 embryos). (D) In mnx MO-injected embryos, MiP express vsx2 but not islet1 (26/60 vsx2+ MiPs in 13 embryos) while CaPs express neither vsx2 nor islet1 (0/60 vsx2+ CaPs in 13 embryos). Scale bar: 10 μm.

Although V2a interneurons are the only cells in the ventral spinal cord that express glutamatergic markers before 32 hpf[37], we also examined expression of vsx2, a definitive V2a marker[13]. In 22 hpf control Tg(nrp1a:GFP) embryos, we found 1.2 vsx2+ cells per spinal hemisegment. In controls, expression of vsx2 and the motoneuron markers islet1 and nrp1a:GFP was mutually exclusive (Figure5C). In the absence of Mnx proteins, we found 2.3 vsx2+ cells per spinal hemisegment. Often, the extra vsx2+ cell weakly expressed GFP and was located near the somite boundary (Figure5D), in the position occupied by the MiP soma, suggesting the hybrid cells expressing both PMN and interneuron markers were MiPs. By comparison, vsx2 was never expressed in CaPs, which continued to express islet2a in the absence of Mnx proteins (Figures3B and5D). These results suggest that Mnx proteins act to block expression of V2a interneuron markers specifically within MiPs.

Mnx proteins regulate MiP axon formation by maintaining Islet1 expression

Previously we found that in the absence of Nkx6.1 and Nkx6.2, most MiPs failed to form dorsal axons, and instead projected both their normal short ventral axon to the muscle pioneers and an interneuron-like axon within the spinal cord[10]. The similarity of the Nkx6 and Mnx knockdown phenotypes suggested that the genes might be part of the same pathway. To test this hypothesis, we injected nkx6 MOs and examined Mnx expression, and we injected mnx MOs and examined Nkx6 expression. We found that mnx expression was unaffected by the absence of Nkx6 proteins (Additional file4: Figure S4). Similarly, nkx6 expression was unaffected by the absence of all three Mnx proteins (Figure5). This indicates that Mnx proteins influence MiP development independently of Nkx6.

Nkx6 proteins initiate a late, MiP-specific phase of Islet1 expression[10]. The MiP dorsal axon phenotype was rescued by co-injection of islet1 mRNA with the nkx6 MOs, demonstrating that it is this late phase of Islet1 that is required for MiPs to form a normal dorsal axon[10]. To learn whether the MiP axon phenotype in mnx MO-injected embryos also depended on the late phase of Islet1 expression, we examined whether this second phase of Islet1 was appropriately expressed in the absence of Mnx proteins. Expression of Islet1 at 18 hpf was normal in the absence of Mnx proteins (Figure2); however, by 21 hpf Islet1 expression in MiPs was either absent or barely detectable (Figure6). This suggests that the second phase of Islet1 expression in MiP is initiated correctly in the absence of Mnx proteins, but that Mnx proteins are necessary to maintain expression of Islet1 in MiP, and that continued Islet1 expression is necessary for MiP to form a normal dorsal axon.

Figure 6
figure 6

Mnx proteins maintain the late phase of Islet1 expression in MiPs independently of Nkx6. (A-D) Single spinal hemisegments of control and mnx MO-injected embryos. MiPs (closed arrowheads) and CaPs (open arrowheads) are indicated in each of the single channel panels; right column shows merged channels. (A) At 17 hpf, MiPs in control embryos strongly express Islet and Nkx6 (17/30 Nkx6+ MiPs in seven embryos). CaPs strongly express Islet but weakly express Nkx6. (B) MiPs in mnx MO-injected embryos continue to strongly express Islet and Nkx6 (13/22 Nkx6+ MiPs in five embryos). (C) At 21 hpf in Tg(nrp1a:GFP) control embryos, both MiPs and CaPs express Islet (32/32 Islet+ CaPs, and 31/32 Islet+ in five embryos. (D) In mnx MO-injected Tg(nrp1a:GFP) embryos, CaPs (60/60 Islet+ CaPs in 10 embryos) but not MiPs (19/60 Islet+ MiPs in 10 embryos), strongly express Islet. Scale bar: 20 μm.

Discussion

We show that the three Mnx transcription factors have dynamic expression patterns in each of the zebrafish PMN subtypes and in VeLD interneurons. Surprisingly, however, Mnx proteins appear dispensable for development of CaP motoneurons and VeLD interneurons. In contrast, Mnx proteins are required for normal specification of MiP motoneurons through regulation of both axon pathfinding and neurotransmitter specificity (Figure7).

Figure 7
figure 7

Mnx proteins promote normal MiP development and suppress acquisition of V2a interneuron and CaP characteristics. (A) Model depicting principal MiP (green) projection errors observed in the absence of Mnx proteins. MiPs often fail to project to their normal dorsal muscle targets and, instead, either project a V2a interneuron-like axon or a motor axon that projects alongside the CaP axon to ventral muscle. Combinations of these three projection errors account for the observed range of MiP phenotypes. By comparison, CaPs (blue) and V2a INs (purple) make normal projections. (B) Genetic pathways that account for observed MiP phenotypes. Mnx proteins, primarily Mnx2a and Mnx2b, promote MiP axogenesis by maintaining the late phase of Islet1 expression initiated by Nkx6. All three Mnx proteins (bracket) suppress acquisition of molecular and morphological features of V2a interneurons, and responsiveness to unknown signals that promote axon growth to ventral muscle.

Mnx expression in interneurons

Spinal cord expression of mnx genes was originally thought to be restricted to motoneurons[1517]. However, the Drosophila melanogaster mnx paralog, hb9, is expressed in both motoneurons and interneurons[38, 39]. More recently, a small population of Mnx1-expressing interneurons was identified in the mouse spinal cord[19]. Here we identify a class of ventral spinal interneurons in zebrafish, VeLDs, that express two mnx genes, mnx1 and mnx2b. The Mnx1-expressing interneurons in mouse are active components in the locomotor central pattern generator[19, 40, 41]. Although these cells have been extensively characterized during fictive locomotion in isolated spinal cord preparations[4247], their exact role in the locomotor network in intact animals is unknown. Indeed, mouse Mnx1+ interneurons have proven resistant to genetic analysis, in part because their developmental provenance is entirely unclear.

It seems unlikely that VeLDs are the zebrafish equivalent of mouse Mnx1+ spinal interneurons. VeLDs are born early, GABA+ and have ipsilateral axons that descend many segments within the spinal cord[4, 8, 27]. In contrast, although the Mnx1+ mouse interneurons may arise from the same domain as motoneurons[3], they are likely to be born later than motoneurons as they have not been described in lineage studies. Mouse Mnx1+ interneurons are glutamatergic and likely make strictly local projections to motoneuron pools within the same segment[42, 46]. We have also noticed some ventromedially-located Mnx1+ interneurons that appear at about three days post-fertilization and do not seem to make projections to adjacent segments. Given the striking parallels between well-characterized components of the locomotor network in zebrafish and mouse[12, 48], it will be important to follow development of these Mnx1+ interneurons in vivo to learn their origins. Assessing their role in zebrafish motor behavior should have implications for understanding the contribution of Mnx1+ interneurons to locomotion in other vertebrate species.

Despite expression in VeLDs, Mnx proteins appear unnecessary for VeLD development. However, we only assayed axon projection and neurotransmitter phenotype, thus our results do not rule out a role for Mnx proteins in regulating some other aspect of VeLD differentiation.

Mnx proteins promote MiP subtype identity

The acquisition of MiP and CaP subtype identities are differentially affected by the absence of Mnx1, Mnx2a and Mnx2b. In the absence of all three Mnx proteins, CaPs fail to down-regulate islet1 expression. However, CaP subtype identity appears unaffected as both axon projection and neurotransmitter expression are normal. This finding is consistent with our previous studies showing that islet1 and islet2a can play equivalent roles in CaP specification[8]. In contrast, a late, MiP-specific phase of islet1 expression is misregulated in the absence of Mnx proteins. In the absence of high levels of Islet1, MiPs fail to form their characteristic dorsal axons. This is reminiscent of the phenotype observed in the absence of Nkx6[10], but whereas Nkx6 proteins are required to initiate the late phase of islet1 expression in MiP, Mnx proteins seem to be required to maintain high levels of Islet1 in MiP, similar to what has been reported in a mouse Mnx1 knock out[16, 17].

Variability in the amount of Islet1 protein or the precise time at which it is cleared might account for variability in MiP morphologies in the absence of Mnx proteins. One possibility is that MiPs that maintain Islet1 expression relatively late retain sufficient motoneuron character to project an axon out of the spinal cord. In contrast, those that down-regulate Islet1 relatively early might fail to express factors necessary to guide growth cones out of the spinal cord and into the periphery. This is consistent with the finding that early expression of Islet1 in CaP is sufficient to permit axon growth into the periphery[8], and could be tested in future experiments with photo-activatable morpholinos[49] to block islet1 translation at different times and assess the frequency with which MiP axons exit the spinal cord.

Surprisingly, when MiPs in mnx MO-injected embryos project axons into the periphery, most of them aberrantly extend to ventral muscle along a pathway normally reserved for CaP axons. Notably, MiP ventral axons stop normally at the muscle pioneers in the absence of Nkx6 proteins and late-phase Islet1 expression[10]. Thus, while Mnx proteins promote formation of dorsal MiP axons by maintaining Islet1 expression, they exclude MiP axons from ventral muscle independently of Islet1.

PMN subtype identity, as revealed by axon trajectory, is influenced by positional signals that normally act during a specific window of developmental time[25, 50]. These signals affect motoneuron subtype, at least in part, by regulating expression of factors involved in axon pathfinding. Motor axons navigate toward their appropriate muscle targets by following subtype-specific guidance cues. The cues that are differentially recognized by CaP axons and MiP axons are unknown. Our results suggest that Mnx proteins regulate expression of receptors that recognize cues that prevent the MiP growth cone from progressing ventral of the muscle pioneers, and thus prevent MiPs from becoming CaP-like. To our knowledge, this is the first report of genes that can cause MiPs to transform to a CaP morphology.

Mnx proteins prevent MiP from acquiring V2a interneuron characteristics

In the absence of Mnx proteins, MiPs, but not CaPs, often form hybrids that have features of both motoneurons and interneurons. Based on expression of vsx2 and vglut and axon morphology, MiPs appear to have acquired features of zebrafish V2a interneurons[12]. As this phenotype is only observed in the combined absence of Mnx1, Mnx2a and Mnx2b, the three zebrafish paralogs act redundantly to suppress the formation of MiP-V2a hybrids. The acquisition of V2a features is reminiscent of the phenotype of Mnx1 knockout mice in which Vsx2 is inappropriately expressed in a subset of Islet1+ motoneurons[16, 17]. However, MN-V2a hybrids in Mnx1 knockout mice fail to project interneuron-like axons within the spinal cord and whether they express glutamatergic markers has not been assessed. Our results suggest that zebrafish MiP-interneuron hybrids acquire a more complete set of V2a features. Regardless, our results reveal a conserved role for the mnx gene family in segregating motoneuron from V2a interneuron cell fate in specific motoneuron subtypes.

We previously reported that knocking down Islet1 resulted in PMNs developing as interneurons and that knocking down the Met receptor tyrosine kinase resulted in PMNs co-expressing motoneuron and interneuron characteristics[8, 35]. In both of these cases, PMNs expressed the neurotransmitter, GABA. Clonal analysis in zebrafish has revealed that PMNs can be siblings with either KA’ or VeLD interneurons[4], both of which express GABA[4, 27]. These observations supported a model whereby many factors expressed by PMNs cooperate to suppress acquisition of characteristics of closely-related interneurons derived from the pMN domain. Here we show that in the absence of Mnx proteins, PMN-interneuron hybrids inappropriately express V2a interneuron characteristics. These data support a model whereby post-mitotic Mnx expression in PMNs suppresses acquisition of characteristics of more distantly-related interneurons from the adjacent p2 domain. A striking aspect of the PMN-V2a phenotype is that it is limited to MiP. This suggests that MiPs are more similar to V2a interneurons than are CaPs. This is consistent with the observation that in the absence of Nkx6 proteins, many MiP-interneuron hybrids have axons with a V2a morphology[10]. However, it is important to note that in our previous Nkx6 knockdown studies, MiPs did not express vsx2[10]. As Mnx proteins suppress vsx2 expression in MiPs (Figure5), we suspect their continued expression in the absence of Nkx6 (Additional file4: Figure S4) accounts for our inability to detect vsx2 expression in MiP in our previous Nkx6 knockdown studies. These combined results imply that other genes in addition to vsx2, genes not regulated by Mnx proteins, contribute to acquisition of V2a interneuron axonal projections.

V2as, like PMNs, originate from a domain that expresses Nkx6.1[12], and continue to express Lhx3 after they exit the cell cycle[29]. Moreover, recent lineage-tracing in mouse has shown that many V2a neurons have expressed Olig2 during their developmental history[51, 52], revealing that they may be even more similar to motoneurons than had been previously appreciated. A more detailed lineage analysis in zebrafish of the relationship between PMNs, VeLD interneurons and V2a neurons could help resolve the relationships among these neurons.

Conclusions

The three zebrafish Mnx transcription factors have distinct expression patterns in each of the zebrafish PMN subtypes and in VeLD interneurons. These expression patterns are dynamic during the period when these cells are extending axons and initiating neurotransmitter expression. Despite their expression in CaP motoneurons and VeLD interneurons, Mnx proteins appear dispensable for development of these two cell types. In contrast, Mnx proteins are required for development of MiP motoneurons. In the absence of Mnx proteins, MiPs extend aberrant axons and express an interneuron-specific neurotransmitter (Figure7).

Methods

Zebrafish

Wild-type (AB), Tg(olig2:GFP)vu12[53], Tg(nrp1a:GFP)js12[36] and Tg(vsx1:GFP)nns5[13] and Tg(mnx1:GFP)ml2[54] zebrafish were maintained in a laboratory breeding colony according to established protocols[55]. Embryos collected from natural crosses were allowed to develop at 28.5°C, and staged by hours post-fertilization (hpf) according to morphological criteria[56].

Generation of transgenic fish lines

A 3-kb fragment of the mnx1 promoter[54] was subcloned into p5E MCS[57]. Multi-site Gateway® technology (Life Technologies; Eugene, OR, USA) was used to assemble an mnx1:GAL4VP16:pA construct flanked by Tol2 terminal inverted repeats. Tg(mnx1:GAL4VP16) lines were generated by co-injecting plasmid DNA and Tol2 transposase RNA[58] into the yolk of one-cell stage embryos. Multiple founders were recovered and characterized; Tg(mnx1:GAL4VP16)b1222 was chosen for this study because transgene expression faithfully mirrored endogenous Mnx1 protein expression (data not shown).

Morpholino injections

Approximately 2.5 nl of 100 μM translation-blocking morpholinos (Gene Tools, LLC; Philomath, OR, USA) against mnx1 (5’-ACCTCACAAACAGATTAACGCCTCG-3’), mnx2a (5’-ACCTCACAAACAGATTAACGCCTCG-3’) and mnx2b (5’-GACTTTTCCATTGCAACACTTTTGT-3’) were injected into one- to two-cell stage embryos; this was sufficient to suppress translation as assayed by whole-mount immunohistochemistry (Additional file5: Figure S5) without elevated cell death as assayed by acridine orange staining (data not shown). These morpholinos have been previously validated[20].

Other previously validated morpholinos used in this study include: random control oligonucleotide (5’-N25-3’), 2.5 nl of 100 μM islet1 E2 (5’-TTAATCTGCGTTACCTGATGTAGTC-3’) plus 100 μM islet1 E3 (5’-GAATGCAATGCCTACCTGCCATTTG-3’)[8] to knockdown islet1; 2.5 nl of 400 μM nkx6.1 (5’-CGCAAGAAGAAGGACAGTGACCCG-3’)[59] plus 400 μM nkx6.2 (5’-CGCGCAAAACTCACCCGCACAGGGA-3’)[10] to knockdown nkx6.1 and nkx6.2; and 2.5 nl of 280 μM lhx3 (5’-GTTCTAACAACATTCTGGCGATAAA-3’) plus 280 μM lhx4 (5’-GCAGCACAGCCGCACTTTGCATCAT-3’) to knockdown lhx3 plus lhx4 (Hutchinson SA, Seredick S, Van Ryswyk L, Talbot JC, Eisen JS: Lhx3 and Lhx4 regulate interneuron fate and prevent motoneurons from co-expressing interneuron characteristics, unpublished). Morpholino effectiveness was verified by whole mount immunohistochemisry.

Fluorescent RNA in situ hybridization

RNA in situ hybridization was performed according to standard protocols[60] with the following modifications. For two-color fluorescent in situ hybridization anti-sense probes were labeled with digoxigenin-UTP (Roche Applied Sciences, Indianapolis, IN, USA) and dinitrophenol-UTP (Perkin-Elmer, Waltham, MA, USA). Following overnight hybridization, unbound probe was removed with three 30-minute washes at 68°C in 50% formamide, 5x SSC and 0.1% SDS, followed by stringent washes in 50% formamide, 2x SSC and 0.1% Tween-20. Labeled probes were detected with HRP-conjugated anti-DIG (1:2,000; Jackson ImmunoResearch, West Grove, PA, USA) or HRP-conjugated anti-DNP (1:2,000; Perkin-Elmer) and stained with fluorescein, Cy3- or Cy5-tyramide (1:100; Perkin-Elmer) for 1 to 10 minutes.

Probes used include mnx1, mnx2a and mnx2b[20]; chat[35]; islet1, islet2a and lhx3[9]; lhx4 (Hutchinson SA, Seredick S, Van Ryswyk L, Talbot JC, Eisen JS: Lhx3 and Lhx4 regulate interneuron fate and prevent motoneurons from co-expressing interneuron characteristics, unpublished).; gad1b and gad2 (collectively referred to as gad), slc17a6a, slc17a6b and slc17a7 (collectively referred to as vglut) and slc6a9 and slc6a5 (collectively referred to as glyt)[28]; vsx2[12]; and gata3[29].

Antibody generation

To prepare Mnx1 and Mnx2b antisera, cDNAs corresponding to amino acids 245 to 311 of Mnx1 or amino acids 224 to 301 of Mnx2b were His-tagged, over-expressed in E. coli and purified by nickel column chromatography under native conditions. These regions are C-terminal to the homeodomain, and are the most divergent regions of the gene family. Purified recombinant proteins were used to immunize rabbits, and the resulting antisera screened by whole mount immunohistochemistry. Attempts to generate antisera against Mnx2a were not successful.

Immunohistochemistry

Embryos were fixed for 2 hours in 4% paraformaldehyde and 1x Fix Buffer[55] at 4°C, and then treated with 0.5% Triton X-100 in 1x PBS for 15 minutes at room temperature. Embryos were blocked in 5% normal goat serum, 2.5% DMSO and 0.1% Tween-20 in 1x PBS before overnight incubation in diluted primary antibody at 4°C. Unbound primary antibodies were removed by washing for two hours in 1x PBS plus 0.1% Tween-20, followed by overnight incubation in diluted secondary antibody at 4°C. Anti-Mnx1, anti-Mnx2a and anti-Mnx2b were detected with HRP-conjugated goat anti-rabbit and stained with fluorescein-, Cy3- or Cy5-tyramide (1:100; Perkin-Elmer) for one minute; all other primary antibodies were detected with dye-labeled secondary antibodies.

Antibodies used include rabbit polyclonal anti-Mnx1 (1:1,000) and anti-Mnx2b (1:1,000), anti-Mnx2a (1:1,000; AnaSpec, Fremont, CA, USA), anti-Lhx3 and anti-Lhx4 (Hutchinson SA, Seredick S, Van Ryswyk L, Talbot JC, Eisen JS: Lhx3 and Lhx4 regulate interneuron fate and prevent motoneurons from co-expressing interneuron characteristics, unpublished), mouse monoclonal anti-Elavl3/4 (1:10,000; A21271, Life Technologies), anti-Gad (1:500; ab11070, Abcam, Cambridge, MA, USA), anti-GFP (JL-8; Clontech, Mountain View, CA, USA; or A-11120, Life Technologies), anti-Histone H3 (phospho S10; 1:1000; ab14955, Abcam), anti-Islet (39.4D5; DSHB, Iowa City, IA, USA), and anti-Nkx6.1 (F55A10; DSHB).

Subtype-specific cell labeling

To correlate cell morphology with gene expression, we injected UAS:EGFP plasmid with Tol2 transposase RNA and selected embryos with GFP-expressing cells for immunohistochemistry. Since our mnx1 morpholino also suppressed expression from our Tg(mnx1:GAL4VP16) transgene, individual neurons in mnx morpholino-injected fish were dye-labeled with 5% tetramethylrhodamine-dextran (D-3308; Life Technologies) in 0.2 M KCl[61].

Image acquisition

All images were acquired on a Zeiss Pascal confocal microscope (Carl Zeiss Microscopy, LLC, Thornwood, New York, USA) using a 40x water immersion objective. The brightness and contrast of images was adjusted using Photoshop CS5 (Version 12.0, Adobe Systems, Inc., San Jose, CA, USA).

Quantification

All observations of PMNs were made in the mid-trunk region of the spinal cord adjacent to somites 8 to 12. We examined at least 30 segments from 10 embryos for each condition, unless otherwise noted in the figure legends.

Abbreviations

CaP:

Caudal primary motoneuron

KA:

Kolmer-Agduhr

Lhx:

LIM homeobox

MiP:

Middle primary motoneuron

Mnx:

Motor neuron and pancreas homeobox

p2:

Progenitor2

PMN:

Primary motoneuron

pMN:

Progenitor of motoneuron

RoP:

Rostral primary motoneuron

VeLD:

Ventral lateral descending.

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Acknowledgements

We thank Marnie Preston and Chris Doe for comments on the manuscript, the Chien lab for Gateway vectors, Dirk Meyer for mnx plasmids, Mike Marusich for help generating Mnx antibodies, and Amanda Lewis, Jacob Lewis, Dayna Lamb, and the UO Zebrafish Facility staff for animal husbandry. Supported by NIH grants NS23915 and HD22486 (JSE), HD007348 (SAH and LVR), and an NSERC fellowship (SS).

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Correspondence to Judith S Eisen.

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The authors declare that they have no competing interests.

Authors’ contributions

SS and LVR participated in the design of the study, carried out molecular experiments, and helped draft the manuscript. SAH generated Mnx antibodies and helped draft the manuscript. JSE conceived of the study, labeled individual neurons, and helped draft the manuscript. All authors read and approved the final manuscript.

Electronic supplementary material

13064_2012_222_MOESM1_ESM.pdf

Additional file 1: Figure S1. mnx1 and mnx2b are both expressed in VeLD interneurons. (A-D) VeLD somata are outlined. (A) At 16 hpf, mnx1 and mnx2b are co-expressed in VeLD. (B) At 24 hpf, mnx1+ VeLDs express gad. (C, D) At 24 hpf mnx1+ VeLDs express neither vsx2 (C) nor vglut (D). Scale bar: 10 μm. (PDF 143 KB)

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Additional file 2: Figure S2. Mnx proteins are restricted to post-mitotic neurons. Lateral views of 12 to 14 hpf Tg(olig2:GFP) embryos. (A) Mnx2a+ cells within the spinal cord do not co-express phosphohistone H3, a marker of mitotic cells (0/153 Mnx2a+ cells in 13 embryos). Some Mnx2a+ cells strongly express GFP. (B) Mnx1+ cells within the spinal cord do not co-express phosphohistone H3 (0/70 Mnx1+ cells in 10 embryos). No Mnx1+ cells strongly express GFP. (C) Mnx2a+ cells that expressed GFP weakly or were GFP- co-expressed Elavl3, a marker of post-mitotic neurons. Mnx2a+ cells that expressed GFP strongly did not co-express Elavl3. (D) Mnx1+ cells co-expressed Elavl3. (E) Schematic of gene expression during transition from pMN progenitors to post-mitotic neurons. Mitotic progenitors express phosphohistone H3 (PH3), whereas post-mitotic neurons express Elavl3. olig2 expression is initiated in progenitors, and down-regulated as cells become post-mitotic. Both Mnx1 and Mnx2a expression is initiated after cells become postmitotic, with expression of Mnx2a preceding expression of Mnx1. Scale bar: 30 μm, A-D. (PDF 228 KB)

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Additional file 3: Figure S3. Mnx proteins are differentially expressed in secondary motoneurons. (A-D) Protein expression in two spinal hemisegments of 26 hpf Tg(mnx1:GFP) embryos. The single channel panels show Mnx protein expression. (A, B) Mnx1 is strongly expressed by PMNs and VeLD interneurons, and more weakly expressed by a subset of mostly dorsally-located secondary motoneurons. (C, D) Mnx2a appears to be down-regulated in PMNs and is expressed by a subset of mostly ventrally-located SMNs. Scale bar: 20 μm. (PDF 430 KB)

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Additional file 4: Figure S4. With the exception of mnx2b which is regulated by Lhx3 and Lhx4, expression of mnx genes is independent of Islet, Nkx6, Lhx3, Lhx4, and other Mnx paralogs. (A AA) Lateral views of control and MO-injected embryos colabeled with islet2a (green) to mark CaP and VaP. Segment boundaries are demarcated with diagonal lines. At 18 hpf, expression of mnx1 (A, B), mnx2a (C, D) and mnx2b (E, F) are unaffected by absence of Islet1. Note that islet2a is not expressed in the absence of islet1[8]. At 18 hpf, expression of mnx1 (A, G), mnx2a (C, H) and mnx2b (E, I) are unaffected by absence of Nkx6.1 and Nkx6.2. At 24 hpf, expression of mnx1 (J, K) and mnx2a (L, M) are unaffected by absence of Lhx3 and Lhx4. mnx2b is not expressed in the absence of Lhx3 and Lhx4 (N, O). At 18 hpf, expression of lhx3 (P, Q) and lhx4 (R, S) are unaffected by absence of Mnx proteins. At 16 hpf, expression of mnx2a (T, U) and mnx2b (V, W) are unaffected by absence of Mnx1. (X AA) Embryos labeled only for expression of mnx genes. Expression of mnx1 (X, Y) and mnx2b (Z, AA) are unaffected by absence of Mnx2a. We did not examine expression of mnx1 and mnx2a in the absence of Mnx2b as we did not detect Mnx2b protein before 20 hpf. Note that panels M, O and Q are reproduced from Figure1 to facilitate comparison of gene expression in control and MO-injected embryos. Scale bar: 10 μm. (PDF 177 KB)

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Additional file 5: Figure S5. Morpholinos targeting mnx family genes are specific and effective in knocking down protein. Lateral views of two spinal hemisegments, segment boundaries denoted by diagonal lines, of uninjected and control MO-injected Tg(mnx1:GFP) embryos labeled for antibodies against Mnx1 (A, D), Mnx2a (B, E), and Mnx2b (C, F). Embryos injected with mnx1 MO lack Mnx1 antibody labeling (G), but maintain Mnx2a (H) and Mnx2b (I) antibody labeling. Embryos injected with mnx2a MO lack Mnx2a antibody labeling (K), but maintain Mnx1 (J) and Mnx2b (L) antibody labeling. Embryos injected with mnx2b MO lack Mnx2b antibody labeling (O), but maintain Mnx1 (M) and Mnx2a (N) antibody labeling. Scale bar: 20 μm. (PDF 144 KB)

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Additional file 6: Figure S6. In the absence of Mnx proteins, neither MiPs nor CaPs aberrantly express GABAergic or glycinergic markers. (A-D) Lateral views of single hemisegments of control and mnx MO-injected embryos. MiPs (closed arrowheads) and CaPs (open arrowheads) are indicated in merged panels (column on right). (A, B) In control and MO-injected embryos, MiP and CaP express chat but not gads. (C, D) In control and MO-injected embryos, MiP and CaP express chat but not glyts. Scale bar: 20 μm. (PDF 319 KB)

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Seredick, S.D., Van Ryswyk, L., Hutchinson, S.A. et al. Zebrafish Mnx proteins specify one motoneuron subtype and suppress acquisition of interneuron characteristics. Neural Dev 7, 35 (2012). https://doi.org/10.1186/1749-8104-7-35

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