- Research article
- Open Access
Shox2 is required for the proper development of the facial motor nucleus and the establishment of the facial nerves
BMC Neuroscience volume 16, Article number: 39 (2015)
Axons from the visceral motor neurons (vMNs) project from nuclei in the hindbrain to innervate autonomic ganglia and branchial arch-derived muscles. Although much is known about the events that govern specification of somatic motor neurons, the genetic pathways responsible for the development of vMNs are less well characterized. We know that vMNs, like all motor neurons, depend on sonic hedgehog signaling for their generation. Similarly, the paired-like homeobox 2b (Phox2b) gene, which is expressed in both proliferating progenitors and post-mitotic motor neurons, is essential for the development of vMNs. Given that our previous study identified a novel role for the short stature homeobox 2 (Shox2) gene in the hindbrain, and since SHOX2 has been shown to regulate transcription of islet 1 (Isl1), an important regulator of vMN development, we sought to determine whether Shox2 is required for the proper development of the facial motor nucleus.
Using a Nestin-Cre driver, we show that elimination of Shox2 throughout the brain results in elevated cell death in the facial motor nucleus at embryonic day 12.5 (E12.5) and E14.5, which correlates with impaired axonal projection properties of vMNs. We also observed changes in the spatial expression of the vMN cell fate factors Isl1 and Phox2b, and concomitant defects in Shh and Ptch1 expression in Shox2 mutants. Furthermore, we demonstrate that elimination of Shox2 results in the loss of dorsomedial and ventromedial subnuclei by postnatal day 0 (P0), which may explain the changes in physical activity and impaired feeding/nursing behavior in Shox2 mutants.
Combined, our data show that Shox2 is required for development of the facial motor nucleus and its associated facial (VII) nerves, and serves as a new molecular tool to probe the genetic programs of this understudied hindbrain region.
In the hindbrain, motor neuron progenitors are born in a region-specific manner, neighboring the floor plate, in response to their level of exposure to different morphogenetic gradients [1, 2]. These neuronal progenitors differentiate in a rhombomere-specific pattern, which requires the correct spatiotemporal expression of the homeotic (Hox) gene clusters [3–6]. Motor neuron progenitors in the hindbrain can differentiate into somatomotor neurons (sMNs), which innervate the skeletal muscles of the body, or visceromotor neurons (vMNs), which innervate autonomic ganglia (general vMNs) and branchial arch-derived muscles (special vMNs) [3, 7, 8]. Facial (VII) motor neurons, which originate from rhombomeres 4/5, belong to the vMN class of motor neurons. At embryonic day 11.25 (E11.25), facial motor neurons begin to migrate caudally to the pial side of the hindbrain to form the facial motor nucleus, which subsequently segregates into two lobes [6, 9, 10]. Despite the elucidation of the genetic mechanisms that specify sMN identity, the corresponding pathways responsible for the establishment of vMNs are less well understood. Furthermore, even though sonic hedgehog (SHH) signaling is known to be required for the development of all motor neurons [7, 11–15], the upstream regulators of Shh expression and function during late embryonic and early postnatal development, especially within the vMNs of the facial motor nucleus, remain largely unknown .
The paired-like homeobox 2b (Phox2b) gene is expressed in both proliferating progenitors and post-mitotic motor neurons and is required for the development of vMNs [17, 18]. Similarly, the homeodomain transcription factor islet1 (ISL1), which is expressed in both post-mitotic sMNs and vMNs, plays a broad role in motor neuron identity and specification [7, 8, 17, 19, 20]. In the absence of Isl1, mice die during embryogenesis around E11.5. This embryonic lethality is associated with an increase in cell death in the hindbrain and neural tube, suggesting that loss of Isl1 function results in the death of cells that were fated to differentiate into motor neurons . In the trigeminal and dorsal root ganglia (DRG), Isl1 appears to play distinct roles during early (i.e. neurogenesis) versus late (i.e. subtype specification) development . In cranial ganglia, Isl1 is required for cell survival and Isl1 mutants show thinner blunted facial (VII) ganglia . However, the precise role of Isl1 in these cell types and in their respective hindbrain nuclei, such as the facial motor nucleus, remains poorly documented.
The adult facial motor nucleus contains seven subnuclei; the lateral, dorsolateral, dorsal intermediate, ventral intermediate, dorsomedial and ventromedial nuclei are located within the main nucleus, while the seventh, the dorsal accessory nuclei, is located above the main nucleus [23, 24]. Neurons innervating the nasolabial musculature are located in the lateral facial motor nucleus, while neurons supplying the auricular musculature are located in the medial facial motor nucleus [23, 24]. Together the lateral, intermediate and medial subnuclei comprise 43, 27.1, and 28.7%, respectively, of the motor neurons in the adult facial motor nucleus, with the dorsal accessory nuclei contributing the final 1.2% .
Studies with mouse knockout models have shown that Shox2 is required for normal development of the humerus and femur [25–27], the anterior palate , the temporomandibular joint of the jaws , the sinoatrial valves and pacemaker region of the heart [30, 31], and TrkB-positive mechanosensory neurons of the dorsal root ganglia . Most recently, Shox2 has been shown to play an important role in development of the inferior colliculus and cerebellum . We suspected a function for Shox2 during facial motor nucleus development given our previous study demonstrating a novel role for Shox2 in the hindbrain , and since SHOX2 has been shown to regulate transcription of Isl1 , an important regulator of vMN development [7, 8, 19, 22]. In the current study we show that conditional inactivation of Shox2 in the brain results in impaired axonal projections of vMNs and a concomitant loss of medially located neurons in the facial motor nucleus postnatally. Furthermore, we demonstrate that Shox2-mutant neonates display impaired feeding behavior, perhaps due to facial paralysis as a result of improper development and function of the facial nerves.
Shox2 expression in the face and facial motor nucleus during development
Whole-mount in situ hybridization (WISH) at E11.5 showed Shox2 expression in the trigeminal (V) and facial (VII) ganglia, in addition to the developing maxillary process and mandibular arch (Figure 1a). Shox2 continued to be expressed in the trigeminal (V) ganglia, maxillary process and mandibular arch at E12.5 (Figure 1b). We also visualized the Shox2 expression pattern with a novel Shox2 lacz allele (described in “Methods”). X-gal staining of embryos carrying the Shox2 lacz allele accurately reproduced the endogenous Shox2 expression pattern with increased sensitivity and less background compared to WISH (Additional file 1: Figure S1). At E10.5, Shox2 lacZ/+ embryos showed lacZ staining in the trigeminal (V) and facial (VII) ganglia of the embryo (Figure 1f). Similarly at E11.5, lacZ staining was visible in the trigeminal (V) and facial (VII) nerves of the embryo, in addition to the maxillary process and mandibular arch (Figure 1g). LacZ continued to be expressed in the trigeminal (V) ganglion of the embryonic face from E12.5 to E13.5, and could be seen in the developing pharyngeal arch (Figure 1h, i). At E14.5 lacZ expression was present in the facial mesenchyme that contributes to the maxilla and mandible (Figure 1j). However, from E12.5 onward lacZ staining was no longer observed in the facial (VII) ganglia (Figure 1h–j). Postnatally (P0) lacZ expression was maintained in the facial mesenchyme surrounding the facial (VII) nerves, but not within the axons themselves (Figure 1k). Examination of Shox2 expression early embryonically in the developing brain showed Shox2 staining in a region of post-mitotic neurons adjacent to the floor plate (Additional file 2: Figure S2A–B), a region where Phox2b+/Isl1+ are localized (Additional file 2: Figure S2C–E) . Later in the P0 brain, Shox2 was expressed in the facial motor nucleus (Figure 1c–e). Similarly, in Shox2 lacZ/+ animals, lacZ staining was strongly expressed in both the lateral and medial lobes of the facial motor nucleus (Figure 1l–o); however, staining was not visible within the trigeminal nucleus (Figure 1n, arrowhead).
Nestin-Cre Shox2-mutant pups exhibit defects in feeding behavior
To determine the functional role of Shox2 in the facial motor nucleus, we used Nestin-Cre  to delete the Shox2 gene conditionally in neural tissue throughout the central nervous system (CNS). We crossed Nestin-Cre; Shox2 +/− mice with Shox2 flox/flox mice  to obtain conditional mutant Nestin-Cre; Shox2 flox/− embryos and neonates. Shox2 expression was eliminated in the brain of Nestin-Cre Shox2-mutant embryos, including the facial motor nucleus (Additional file 3: Figure S3C–D, dashed-circle). All Nestin-Cre Shox2-mutant pups died between 18 to 26 h following birth. This limited our characterization of Shox2 function to embryonic and neonatal stages. P0 Nestin-Cre; Shox2 flox/− mutant pups displayed reduced activity and impaired feeding behavior as early as 6 h following birth (Additional file 4: Movie 1), which correlated with a lack of milk in the stomachs of Nestin-Cre; Shox2 flox/− mutant pups (Additional file 3: Figure S3E, arrows). Since Shox2 is required for the proper development of the palate , we analyzed the anterior and posterior palate of Nestin-Cre; Shox2 flox/− mutant pups. We did not observe any obvious defects or malformations in the palate of Nestin-Cre; Shox2 flox/− mutant pups (Additional file 3: Figure S3F–K), suggesting that the absence of milk in Shox2-mutant neonatal stomachs was not due to cleft palate malformations. Nestin-Cre; Shox2 flox/− mutant pups also displayed tremors 16–26 h following birth (Additional file 4: Movie 1), which could be related to defects in neural circuitry or result from a loss of Shox2 function in other regions of the hindbrain.
Facial (VII) nerve branching defects in Nestin-Cre Shox2-mutant animals
Since Shox2-mutant neonates displayed impaired feeding but an apparently normal palate, we hypothesized that Shox2 mutants fail to nurse properly due to facial paralysis. To test this hypothesis, we first sought to determine if the abnormal feeding behavior resulted from the loss of a subset of axons in the nerves of the face. We stained control and Nestin-Cre Shox2-mutant embryos and P0 heads with the 2H3 antibody that visualizes nerves by detecting neurofilaments (Figure 2). In E11.5 Nestin-Cre; Shox2 flox/− conditional knockout embryos the trigeminal nerves (V) appeared normal (Figure 2a–b, arrowheads). To confirm that the trigeminal nerves (V) were intact even in the complete absence of Shox2, we performed neurofilament staining on E11.75 Shox2-null embryos (Figure 2c–d, arrowheads) . While the trigeminal nerves (V) remained intact, the facial nerves (VII) were truncated and failed to branch properly in both Nestin-Cre; Shox2 flox/− conditional knockout and Shox2-null embryos (Figure 2a–d, arrows). At E12.5 the facial (VII) nerves continued to be truncated as compared to controls (Figure 2e–h, dashed-box). Neurofilament staining at E12.5 displayed a range in severity of facial (VII) nerve truncation, with Figure 2f showing the least severe truncation and Figure 2h having the most severe truncation we observed among seven embryos. Later at E13.5 (Figure 2i), E14.5 (Figure 2k), and early postnatal (P0; Figure 2m) stages, the zygomatic, superior buccolabial, inferior buccolabial and marginal mandibular nerve branches of the facial (VII) nerve could be seen in controls (Figure 2i, k, m) , however these distinct facial (VII) nerve branches were truncated or absent in Nestin-Cre; Shox2 flox/− mutant animals (Figure 2j, l, n; arrows). Similar to E12.5, facial (VII) nerve truncation ranged in severity at the later embryonic and early postnatal time-points analyzed (data not shown). The severity in facial (VII) nerve truncation observed in Nestin-Cre; Shox2 flox/− mutant animals, displayed in Figure 2j, l, n, are representative of the most common truncations observed.
To confirm the persistent lack of proper facial (VII) nerve branching and development, particularly at late embryonic and early postnatal time-points when the larger head size led to confounding background staining, we used a second transgenic line, this one carrying a bacterial artificial chromosome (BAC) containing the Shox2 gene with a lacZ insertion (previously described BAC RP23-105B3-lacZ transgenic line ) to visualize the facial (VII) nerves. While obvious facial (VII) nerve truncations were difficult to visualize at E11.5 (Figure 3a, b), the main branch of the facial (VII) nerve was noticeably truncated, as the smaller ganglionic projections were absent at E12.5 in Nestin-Cre; Shox2 flox/− mutant embryos as compared to controls (Figure 3c–d, arrow). Furthermore, consistent with our neurofilament staining, at later embryonic (E13.5 and E14.5) and early postnatal (P0) stages, the zygomatic, temporal, superior buccolabial, inferior buccolabial and marginal mandibular nerve branches of the facial (VII) nerve were observed in controls (Figure 3e, g, i) and appeared truncated or absent in Nestin-Cre; Shox2 flox/− mutant animals (Figure 3f, h, j; arrows). For example, by P0 the facial (VII) nerves appeared to be absent in Nestin-Cre; Shox2 flox/− mutant animals (Figure 3j, arrows). The buccal and superficial masseter nerves, both sensory components originating from the trigeminal (V) nerve , were the only nerves visible in Nestin-Cre; Shox2 flox/− mutant animals, leaving the face almost completely devoid of innervation (Figure 3j, arrows). To determine whether the facial (VII) nerve disruptions occurred as a result of the slight reduction in Shox2 expression in the embryonic facial mesenchyme (Additional file 3: Figure S3A–B, arrows), or whether this was related specifically to disruptions in the facial motor nucleus, we conditionally removed Shox2 in all neural crest derivatives using a Wnt1-Cre driver. This resulted in the complete loss of Shox2 expression in the face (Additional file 5: Figure S4A, B), and ultimately did not appear to result in any disruptions to the development of the facial (VII) nerves (Additional file 5: Figure S4C, D). Together these results show impaired axonal projection properties of visceral motor neurons (vMNs) in the facial motor nucleus of the hindbrain in mice lacking Shox2.
Loss of Shox2 in the facial motor nucleus results in elevated apoptosis
Since Shox2-mutant embryos and neonates display impaired axonal projection properties and were unable to nurse properly, we next wanted to determine if development of the facial motor nucleus was disrupted in the absence of Shox2. Both neurofilament and lacZ staining of P0 control and Nestin-Cre; Shox2 flox/− or Nestin-Cre; Shox2 lacZ/flox pup brains demonstrated that the facial motor nucleus was severely reduced in size, with disruptions in neuronal spatial organization in mice lacking Shox2 function (Figure 4a–f, arrows; note that the Shox2 lacZ allele is a null or severely hypomorphic allele, see “Methods”). While the symmetry between the left and right facial motor nuclei appears to be relatively maintained (Figure 4c–d, arrows), the two lobes that normally comprise the facial motor nucleus are no longer present (Figure 4e–f, arrows). We next investigated whether an increase in apoptosis could account for the changes observed in the facial motor nucleus of Shox2-mutant brains. We found an increase in the number of apoptotic cells present at E12.5 and E14.5 in the facial motor nucleus of Shox2-mutants (Figure 4g–l); however, no significant increase in apoptosis was detected in the E16.5 or P0 facial motor nucleus of Shox2-mutant animals (Figure 4m–r). We observed a ~7.5-fold increase in the number of cleaved active-CASP3 + cells in the E12.5 facial motor nucleus of Nestin-Cre; Shox2 flox/− animals as compared to controls (Figure 4i; control n = 3, Nestin-Cre; Shox2 flox/− n = 3, p = 0.0038). We also observed a striking ~17.7-fold increase in the number of cleaved active-CASP3 + cells in the E14.5 facial motor nucleus of Nestin-Cre; Shox2 flox/− animals as compared to controls (Figure 4l; control n = 3, Nestin-Cre; Shox2 flox/− n = 3, p = 0.0007). While the slight elevation in apoptosis detected in the E16.5 and P0 facial motor nucleus of Shox2-mutant animals was not significantly different from controls (Figure 4o, r), we did observe a ~3.5-fold increase in the number of cleaved active-CASP3 + cells at P0 when we included the tissue immediately surrounding the facial motor nucleus of Nestin-Cre; Shox2 flox/− animals (Figure 4p–q, entire panel including cells within the dashed-circle) in our cell count (Figure 4s; control n = 3, Nestin-Cre; Shox2 flox/− n = 3, p = 0.0007). Moreover, when we calculated the area of Shox2lacZ + cells remaining in sagittal sections through the center of the facial motor nucleus of Nestin-Cre; Shox2 lacZ/flox animals as compared to controls at E14.5 (Figure 4t) and P0 (Figure 4u), we observed a ~44% decrease in the area of Shox2lacZ + cells in the E14.5 facial motor nucleus (Figure 4v; control n = 3, Nestin-Cre; Shox2 lacZ/flox n = 3, p = 0.0027) and a ~53% decrease in the area of Shox2lacZ + cells in the P0 facial motor nucleus (Figure 4w; control n = 3, Nestin-Cre; Shox2 lacZ/flox n = 3, p = 0.0011). Therefore, the higher levels of apoptosis are correlated with a decrease in the size of the facial motor nucleus, and taken together, the results demonstrate that apoptosis contributes to the disruptions observed in the facial motor nucleus of Nestin-Cre; Shox2 flox/− animals.
Shox2 is required for normal expression of markers of vMN identity in the facial motor nucleus
Given the marked reduction in size of the facial motor nucleus in Shox2 mutants (Figure 4), we next sought to investigate whether factors other than facial (VII) nerve truncation and cell death could be changing in the facial motor nucleus following the loss of Shox2. Prior to E14.5, we did not observe any obvious changes in gene expression or disruptions to the migratory patterns of vMNs (Additional file 2: Figure S2F-K, M-R). At E14.5, however, sagittal sections of the facial motor nucleus showed reductions in the overall size of the nucleus in Nestin-Cre; Shox2 lacZ/flox embryos (Figure 5b), which was consistent with the regional increase in the number of cleaved active-CASP3 + cells at this time-point (Figure 4k). Since SHOX2 has been previously shown to regulate Isl1 , an important regulator of vMN development [7, 19, 22], we next examined the expression of Isl1 in Shox2-mutant animals. We observed a regionally restricted loss of Isl1 and the hindbrain vMN determinant Phox2b in the facial motor nucleus as early as E14.5 in Nestin-Cre; Shox2 flox/− mutant embryos as compared to controls (Figure 5e–h, arrows). Since loss of Isl1 function in the trigeminal and DRG have been shown to result in changes in the expression of contactin 2 (Cntn2), tubulin β-3 chain (Tubb3) and peripherin 1 (Periph) , and given that Phox2b-deficient mice have been used to identify the facial motor nucleus as a source of Slit homolog 2 (Slit2) signaling , we next examined the expression patterns of these genes. Although subtle changes in the spatial patterns and expression levels of Cntn2 and Tubb3 were observed, Periph1, solute carrier family 18 (Slc18a3) and Slit2 phenocopied the regionally specific absence of Isl1 and Phox2b in the facial motor nucleus at E14.5 in Nestin-Cre; Shox2 flox/− mutant embryos (Figure 6i–r, dashed-circle and arrows). The changes in expression for these genes continued to be observed between Nestin-Cre; Shox2 flox/− mutant embryos and controls at E16.5 (data not shown). Together, these results show that Shox2 is required for normal expression of markers of vMN identity at E14.5.
Loss of Shox2 results in severe developmental disruptions to the facial motor nucleus
In contrast to the subtle changes at E14.5, postnatally we observed a drastic reduction in the size of the facial motor nucleus and changes to the overall organization of motor neurons in Nestin-Cre; Shox2 flox/− mutant animals (Figure 6), consistent with the phenotype displayed in Figure 4. Specifically, lacZ staining of P0 control and Nestin-Cre; Shox2 lacZ/flox sagittal sections of the facial motor nucleus demonstrate that the nucleus is reduced in size in mice lacking Shox2 (Figure 6b). The expression levels of Isl1, Phox2b, Cntn2, Tubb3, Periph, Slc18a3 and Slit2 were all strikingly reduced in the P0 facial motor nucleus of Nestin-Cre; Shox2 flox/− mutant animals as compared to controls (Figure 6e–r, dashed-circle). Since conditional inactivation of Shox2 in the brain was previously shown to result in the down-regulation of Shh expression in dorsal-residing Purkinje cells of the cerebellum , we next investigated whether loss of Shox2 function in the facial motor nucleus interfered with the expression of Shh. The expression of both Shh and patched 1 (Ptch1) were absent in the facial motor nucleus of Nestin-Cre; Shox2 flox/− mutant animals (Figure 6s–v).
Although the loss of Shox2 in the brain resulted in drastic reductions in the size of the facial motor nucleus and the expression of the above-mentioned genes, the spared vMNs remaining in the facial motor nucleus of Shox2 mutants appeared to be mostly localized to the dorsal regions of the nucleus (Figure 6B″, f, n). This suggested that there could be a region-specific loss of distinct subnuclei in the facial motor nucleus in Shox2-mutant animals. Therefore we examined the expression patterns of these same genes in coronal sections of the facial motor nucleus, as this would allow us to more clearly observe the six subnuclei that comprise the main facial motor nucleus; specifically the lateral, dorsolateral, dorsal intermediate, ventral intermediate, dorsomedial and ventromedial nuclei [23, 24]. LacZ staining of P0 control and Nestin-Cre; Shox2 lacZ/flox coronal sections of the facial motor nucleus demonstrated that elimination of Shox2 resulted in the loss of medially-localized subnuclei, specifically the dorsomedial and ventromedial nuclei, in addition to severe disruptions to the development of the intermediate nuclei, especially the dorsal intermediate (Figure 7b). Similar to what we observed at P0 in sagittal sections of the facial motor nucleus (Figure 6), the expression of Isl1, Phox2b, Cntn2, Tubb3, Periph, Slc18a3, Slit2, Shh and Ptch1 were restricted to the lateral or intermediate regions in coronal sections of the facial motor nucleus, or completely lost in Nestin-Cre; Shox2 flox/− mutant animals as compared to controls (Figure 7e–v, dashed-circle). While the regional changes in expression were variable between the genes examined, in general the dorsomedial, ventromedial and dorsal intermediate subnuclei of the facial motor nucleus appeared to be most strongly affected in Shox2-mutant animals (Figure 7), which may reflect a regional specific requirement for Shox2 in the facial motor nucleus or may indicate that there are populations of vMNs within the facial motor nucleus that do not express Shox2 during development. Together, the results suggest that Shox2 is required for the development of specific subcompartments within the broader facial motor nucleus.
In this study, we used a Nestin-Cre driver and a conditional knockout strategy to determine the contribution of Shox2 to the development of the facial motor nucleus. We found that mice lacking Shox2 function failed to develop proper vMNs in the medial subnuclei normally present in the facial motor nucleus, which was accompanied by truncated or absent facial (VII) nerve projections. Our results have uncovered an unexpected and novel role for Shox2 in the development of the facial motor nucleus and facial (VII) nerves. Specifically, Shox2 is required for cell survival and perhaps plays a region-specific role in the development and/or maintenance of normal transcriptional programs of vMNs of the facial motor nucleus. Ultimately, in the absence of Shox2, pups lack facial (VII) nerves and display abnormal feeding behavior.
Shox2 is required for cell survival in the facial motor nucleus
Nestin-Cre-mediated deletion of Shox2 in the brain resulted in a significant increase in the number of apoptotic cells present at E12.5 and E14.5 in the facial motor nucleus of Shox2-mutants. Given that truncated and abnormal facial (VII) nerve projections could be observed in Nestin-Cre; Shox2 flox/− mutants from E11.5 onward, apoptosis could: (1) contribute to the disruptions in the axonal projection properties of vMNs in the facial motor nucleus, or (2) result from a lack of peripheral trophic support for the facial (VII) nerves in Shox2 mutants. Similarly, the changes observed in the size of the P0 facial motor nucleus also likely results from elevated cell death embryonically in Shox2-mutant animals. However, given that there are ~6,400 neurons that comprise the facial motor nucleus [23, 24], future analysis is needed to quantify cell death accurately over a developmental time course to determine if the levels of cell death we observe in Shox2-mutant animals is sufficient to account for the disruptions observed in the facial motor nucleus in the absence of Shox2. This is similar to what has been documented in Isl1 mutants, as loss of Isl1 is associated with increased cell death in the trigeminal, DRG, hindbrain and neural tube prior to E14.5, while later developmentally Isl1 functions during subtype specification [19, 21, 22, 38]. Accordingly, if Shox2 is required to maintain proper Isl1 expression in vMNs of the facial motor nucleus, similar to what has been observed during heart development , and Isl1 is required to induce the subsequent differentiation of adjacent neurons, similar to what has been observed in the neural tube , this could explain the elevated cell death observed in neurons adjacent to the facial motor nucleus at P0. Pattyn et al.  have shown that unlike PHOX2B and ISL1, NKX6 proteins (NKX6.1 and NKX6.2) are not required for the establishment of vMN identity, yet NKX6 proteins are necessary to prevent vMNs from trans-differentiating into improper neuronal subtypes. Similar to Shox2 mutants, mice lacking Nkx6 function display impaired axonal projection properties of vMNs and facial nerve disruptions . Together, the Shox2-mutant model could provide an additional example to support the argument of Pattyn et al. that vMN differentiation requires multiple inputs rather than one dominant determinant . Alternatively, necrosis in the facial motor nucleus region could be responsible for the observed ectopic increase in the number of apoptotic cells in tissue immediately surrounding the facial motor nucleus.
Shox2 may play a regional specific role in the transcriptional programs of vMNs during development of the facial motor nucleus
In this study we have shown that Shox2 is expressed in the facial motor nucleus and provide evidence that Shox2 plays an important role during facial motor nucleus development. We have demonstrated that loss of Shox2 function results in the down-regulation or loss of Isl1, Phox2b, Cntn2, Tubb3, Periph, Slc18a3 and Slit2 in the facial motor nucleus. Since loss of Isl1 function in the trigeminal and DRG have been shown to result in changes in the expression of Cntn2, Tubb3 and Periph , and given that Phox2b-deficiency influences Slit2 expression , we propose that the observed changes in gene expression in Shox2 mutants could result from direct or indirect regulation of Isl1 and/or Phox2b by SHOX2. Since Isl1 can rescue Shox2-mediated bradycardia, and Isl1 has been shown to be a transcriptional target of SHOX2 in vitro , it would not be surprising if SHOX2 regulates Isl1 in the facial motor nucleus.
As conditional inactivation of Shox2 in the brain was previously shown to result in the down-regulation of Shh expression in dorsal-residing Purkinje cells of the cerebellum , we also investigated whether loss of Shox2 function in the facial motor nucleus interfered with expression of Shh. Similar to what was observed in the cerebellum, the expression of both Shh and Ptch1 were reduced or lost in the facial motor nucleus of Shox2-mutant animals, suggesting that Shox2 acts upstream of SHH signaling, or that the neurons that would normally express Shh underwent apoptosis earlier embryonically in Shox2-mutant animals. Despite the known critical function of Shh in motor neuron generation [7, 11–15], the role of Shh in the later development of the vMNs of the facial motor nucleus remains largely unknown. In rats, SHH appears to play a role in the regeneration of the facial motor nucleus and facial (VII) nerves following nerve injury . Therefore, as the facial motor nucleus normally undergoes massive cell death from E19 to P10 , the late-onset of Shh expression in the facial motor nucleus could be localized to specific vMNs for cell survival. This hypothesis will be tested in future studies. Together, it appears that Shox2 is necessary for proper Isl1 and Phox2b expression levels in the developing facial motor nucleus, and is subsequently required for late-onset Shh expression; whether this results from facial (VII) nerve disruption and embryonic apoptosis in Shox2 mutants or occurs via direct or indirect regulation of Isl1, Phox2b and/or Shh has yet to be determined.
Since the phenotype observed in the facial motor nucleus of Shox2 mutants, including the changes in gene expression, were most prominent in the medial and intermediate subnuclei, factors other than SHOX2 must contribute to the development and survival of the lateral subnuclei of the facial motor nucleus. The observed phenotype could reflect a regional specific requirement for Shox2 in the facial motor nucleus or indicate that there are populations of vMNs within the facial motor nucleus that do not express Shox2. The latter hypothesis is supported by results depicted in Figure S2F, H, J, as the Shox2 expression domain appears more restricted then those of Isl1 and Phox2b; therefore, future analysis will be required to examine whether SHOX2−/ISL1+ and/or SHOX2−/PHOX2B+ cell populations exist in the facial motor nucleus. Alternatively, if vMNs destined for the lateral subnuclei of the facial motor nucleus are specified first, this could explain why they are the least disrupted group of nuclei apparent in Shox2 mutants. However, considering the severe disruptions to facial (VII) nerve development observed in Shox2 mutants, including those that innervate the nasolabial musculature that are supplied by neurons located in the lateral subnuclei of the facial motor nucleus [23, 24], it is also possible that Shox2 is required for the proper development of the lateral facial motor nuclei. This is further supported by changes in the expression of Cntn2, Tubb3, Shh and Ptch1 in the lateral facial motor nucleus. Taken together, it appears that Shox2 may play a role in the transcriptional programs of vMNs during development of the facial motor nucleus; whether this occurs via a regional requirement for Shox2 in the facial motor nucleus or influences the development of the entire facial motor nucleus in an equal manner has yet to be determined.
Disruptions in the development of the facial motor nucleus influences the axonal projections of vMNs of the facial (VII) nerves in Shox2-mutant animals
As Shox2-mutant neonates display impaired feeding behavior, we wondered if this was due to a loss of a subset of axons in the nerves present in the face or whether it reflected a more substantial innervation deficit. Our findings demonstrate that the loss of Shox2 causes severe truncations and disruptions to the development of the facial (VII) nerves, which could result from: (1) a lack of peripheral trophic support for the facial (VII) nerves, (2) vMN cell death, (3) facial motor nucleus defects that influence the axonal projections of vMNs and target acquisition of the facial (VII) nerves, or a combination thereof. It should be mentioned, however, that disruptions in peripheral trophic support for the facial (VII) nerves would have to result from Shox2’s autonomous function in the facial (VII) nerves themselves, and not as a result of Shox2 playing a role as a peripheral target, since loss of Shox2 expression in the face in Wnt1-Cre; Shox2 flox/− mutant animals does not disrupt facial (VII) nerve development.
Given that the face of Shox2-mutant neonates are severely devoid of innervation, the behavioral abnormalities exhibited by Shox2-mutant animals could be attributed to facial paralysis. Disruption of Hoxb1 function has been shown to result in facial nerve defects in mice, where the phenotype is similar to that of human patients with Bell’s Palsy or Moebius Syndrome . Similarly, other Hox-mutant mouse models have displayed disruptions in facial (VII) nerve development, which correlate with facial impairments . Moreover, Isl1 mutants display disruptions in the development of the facial (VII) nerves, however similar to Shox2 mutants, early postnatal lethality has limited the behavioral analysis of these animals [21, 22, 38]. To determine if disruption to the facial motor nucleus is the cause of the early postnatal lethality of Nestin-Cre; Shox2 flox/− animals, future studies could employ more restricted hindbrain Cre lines to specifically remove Shox2 expression from the facial motor nucleus. If regionally restricted loss of Shox2 in facial motor nucleus does not result in postnatal lethality, future studies could examine Shox2-mutant behavior later postnatally and in the adult to test whether Shox2-mutant animals have control over their face or are experiencing facial paralysis.
Taken together, these results demonstrate that elimination of Shox2 in the brain results in disruptions in the development of the facial (VII) nerves and the facial motor nucleus. The present study demonstrates that in the absence of Shox2 the murine face develops with severe innervation deficits, ultimately highlighting the importance of Shox2 to proper facial motor nucleus development. The Shox2-mutant model can now be exploited to further our understanding of normal neuronal development and circuit formation; processes that are likely dysregulated in human facial paralysis disorders.
To generate conditional Shox2 knockout animals, mice bearing the Nestin-Cre transgene , in addition to a wild-type and deleted Shox2 allele, were crossed to mice carrying two floxed Shox2 alleles . Shox2 mutants were positive for Nestin-Cre and carried one deleted and one floxed Shox2 allele. Littermate control animals carried either one or two functional copies of Shox2, as no changes in the gross morphology of the facial motor nucleus or facial nerves were observed in heterozygotes. We designated embryonic day 0.5 (E0.5) to be noon on the day a plug was detected. Mice were maintained on a mixed C57BL/6-129/Sv background. Mice carrying the deleted and floxed Shox2 alleles were described previously , while mice carrying the Nestin-Cre transgene were from the Jackson Laboratory (Bar Harbor, ME), and described previously . BAC RP23-105B3-lacZ transgenic animals were described previously , while Shox2 lacZ mice are described below. All experiments performed at the University of Calgary were approved by the Life and Environmental Sciences Animal Care Committee. Experiments were conducted on three embryos or neonates of a particular genotype at each gestational and postnatal time point described, unless otherwise stated.
Generation and characterization of Shox2 lacZ mice
Shox2 lacZ mice were produced by pronuclear injection of a 15.4 kb NarI fragment (Additional file 1: Figure S1A) of BAC RP23-103D17-lacZ that has a lacZ cassette inserted in the Shox2 gene as previously described . One of seven transgenic lines carrying this transgene showed an unexpected expression pattern that recapitulated all of the expression domains of the endogenous Shox2 gene (compare Additional file 1: Figure S1D–S1E), despite evidence that the regulatory regions controlling expression in most of these domains is not within the transgene sequence . This result suggested that the transgene in this line, designated Shox2 lacZ may have inserted into the Shox2 locus. Although rare, targeting of transgenic constructs generated by pronuclear injection has been reported [41, 42]. We confirmed a loss of Shox2 function by a complementation test and targeting was shown by long range PCR (Additional file 1: Figure S1B). For the former, the Shox2 lacZ allele was combined with the Shox2 − allele. Mice with the genotype Shox2 lacZ/− died at birth with defects similar to Shox2 null animals, showing non-complementation (the limb and palate phenotypes are shown in Additional file 1: Figure S1F–K, respectively). Long-range PCR was performed with a forward primer corresponding to a sequence 4.5 kb upstream of Shox2 (327 bp upstream of the 5′ limit of the transgene) and a reverse primer within the lacZ sequence. These primers amplified a 5.2 kb PCR product from DNA of Shox2 lacZ mice as expected if the transgene were inserted at the Shox2 genomic locus (Additional file 1: Figure S1B). Furthermore, western blotting failed to detect SHOX2 protein in lysates from E11.5 limb buds of Shox2 lacz/lacZ embryos while lysates from wild-type littermate embryos showed clear SHOX2 signal (data not shown). Therefore we conclude that the Shox2 lacZ allele is a null or severely hypomorphic allele. The precise molecular nature of the transgene insertion at its 3′ end has not yet been determined.
Embryos with lacZ transgenes were stained with X-gal according to standard techniques . ImageJ was used to determine the relative size of the facial motor nucleus in lacZ stained control and NestinCre; Shox2 lacZ/flox sagittal sections at E14.5 and P0 (Figure 4t–u).
In situ hybridization
Whole-mount in situ hybridization (WISH) with a riboprobe was previously described . In situ hybridization (ISH) on cryosections was previously described . The Shox2 , Shh  riboprobes have been described elsewhere. PCR primers used for generating the Ptch1 riboprobe are as follows: Fwd: GGGAGGAAATGCTGAATAAAGCC and Rev: CCAGGAGGAAGACATCATCCACAC, while the primers used for generating the Isl1, Cntn2, Tubb3, Periph, Slc18a3, Phox2b, and Slit2 riboprobes were obtained from the Allen brain atlas website (http://www.brain-map.org). DIG labeled riboprobes were detected with an AP-conjugated anti-DIG antibody (Roche) and BM Purple AP (Roche) was used as the color development substrate. All samples/slides used for comparisons were processed together. Following staining, tissue sections were mounted using Aqua Poly/Mount (Polysciences Inc.). ISH images were taken with a Leica MZ12.5 stereomicroscope using the associated Leica software. Brightness and/or contrast of the entire image was adjusted using Adobe Photoshop CS5.1 if deemed appropriate.
Dissected embryos and postnatal brains were placed in ice-cold PBS, and fixed in 4% paraformaldehyde (PFA) overnight at 4°C. The tissue was washed in PBS and equilibrated in 30% sucrose/PBS overnight at 4°C. Both embryos and postnatal brains were embedded in Tissue Freezing Medium (TFM, Triangle Biomedical Sciences) and cryosectioned (16–20 μm sections). For immunohistochemistry (IHC), cryosections were rehydrated in PBS, washed with PBT (0.1% Triton-X), blocked using 5% normal goat serum (NGS) for 2 h at room temperature, and exposed to anti-active Caspase-3 (1:400, BD Pharmingen or 1:500, Promega) at 4°C overnight. Slides were then washed with PBT and exposed to secondary antibody (1:200, alexa 488 goat-anti-rabbit, Life Technologies) for 2 h at room temperature. Sections were mounted using Aqua Poly/Mount (Polysciences Inc.). Fluorescent IHC images were captured on a Zeiss LSM710 confocal microscope.
Antibodies recognizing neurofilaments (2H3) were used to visualize nerves in embryos or postnatal day 0 (P0) pup heads (skin was removed at P0). Samples were fixed at least 4 h in Dent’s fixative (4:1, Methanol:DMSO). Embryos and P0 heads were processed according to standard techniques previously described . The 2H3 antibody was developed by T. Jessell/J. Dodd  and was obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biology, Iowa City, IA 52242.
Quantification methods and statistical analysis
Quantitative results for cell counts are represented by mean scores ± S.E.M. and were analyzed by two-tailed unpaired t tests using Prism 3 for Macintosh (GraphPad Software, La Jolla, CA, USA).
Lumsden A, Keynes R (1989) Segmental patterns of neuronal development in the chick hindbrain. Nature 337:424–428
Herrup K, Diglio TJ, Letsou A (1984) Cell lineage relationships in the development of the mammalian CNS. I. The facial nerve nucleus. Dev Biol 103:329–336
Gavalas A, Ruhrberg C, Livet J, Henderson CE, Krumlauf R (2003) Neuronal defects in the hindbrain of Hoxa1, Hoxb1 and Hoxb2 mutants reflect regulatory interactions among these Hox genes. Development 130:5663–5679
Gaunt SJ, Krumlauf R, Duboule D (1989) Mouse homeo-genes within a subfamily, Hox-1.4, -2.6 and -5.1, display similar anteroposterior domains of expression in the embryo, but show stage- and tissue-dependent differences in their regulation. Development 107:131–141
Dolle P, Lufkin T, Krumlauf R, Mark M, Duboule D, Chambon P (1993) Local alterations of Krox-20 and Hox gene expression in the hindbrain suggest lack of rhombomeres 4 and 5 in homozygote null Hoxa-1 (Hox-1.6) mutant embryos. Proc Natl Acad Sci USA 90:7666–7670
Studer M, Lumsden A, Ariza-McNaughton L, Bradley A, Krumlauf R (1996) Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1. Nature 384:630–634
Pattyn A, Vallstedt A, Dias JM, Sander M, Ericson J (2003) Complementary roles for Nkx6 and Nkx2 class proteins in the establishment of motoneuron identity in the hindbrain. Development 130:4149–4159
Tsuchida T, Ensini M, Morton SB, Baldassare M, Edlund T, Jessell TM et al (1994) Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes. Cell 79:957–970
Auclair F, Valdes N, Marchand R (1996) Rhombomere-specific origin of branchial and visceral motoneurons of the facial nerve in the rat embryo. J Comp Neurol 369:451–461
Garel S, Garcia-Dominguez M, Charnay P (2000) Control of the migratory pathway of facial branchiomotor neurones. Development 127:5297–5307
Traiffort E, Charytoniuk D, Watroba L, Faure H, Sales N, Ruat M (1999) Discrete localizations of hedgehog signalling components in the developing and adult rat nervous system. Eur J Neurosci 11:3199–3214
Jessell TM (2000) Neuronal specification in the spinal cord: inductive signals and transcriptional codes. Nat Rev Genet 1:20–29
Briscoe J, Chen Y, Jessell TM, Struhl G (2001) A hedgehog-insensitive form of patched provides evidence for direct long-range morphogen activity of sonic hedgehog in the neural tube. Mol Cell 7:1279–1291
Briscoe J, Pierani A, Jessell TM, Ericson J (2000) A homeodomain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube. Cell 101:435–445
Ericson J, Morton S, Kawakami A, Roelink H, Jessell TM (1996) Two critical periods of Sonic Hedgehog signaling required for the specification of motor neuron identity. Cell 87:661–673
Akazawa C, Kohsaka S (2007) In vivo characterization of sonic hedgehog in the peripheral nerve regeneration. Brain Nerve 59:1341–1346
Dubreuil V, Hirsch MR, Pattyn A, Brunet JF, Goridis C (2000) The Phox2b transcription factor coordinately regulates neuronal cell cycle exit and identity. Development 127:5191–5201
Pattyn A, Hirsch M, Goridis C, Brunet JF (2000) Control of hindbrain motor neuron differentiation by the homeobox gene Phox2b. Development 127:1349–1358
Pfaff SL, Mendelsohn M, Stewart CL, Edlund T, Jessell TM (1996) Requirement for LIM homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation. Cell 84:309–320
Thor S, Ericson J, Brannstrom T, Edlund T (1991) The homeodomain LIM protein Isl-1 is expressed in subsets of neurons and endocrine cells in the adult rat. Neuron 7:881–889
Sun Y, Dykes IM, Liang X, Eng SR, Evans SM, Turner EE (2008) A central role for Islet1 in sensory neuron development linking sensory and spinal gene regulatory programs. Nat Neurosci 11:1283–1293
Liang X, Song MR, Xu Z, Lanuza GM, Liu Y, Zhuang T et al (2011) Isl1 is required for multiple aspects of motor neuron development. Mol Cell Neurosci 47:215–222
Ashwell KW (1982) The adult mouse facial nerve nucleus: morphology and musculotopic organization. J Anat 135:531–538
Ashwell KW, Watson CR (1983) The development of facial motoneurones in the mouse—neuronal death and the innervation of the facial muscles. J Embryol Exp Morphol 77:117–141
Cobb J, Dierich A, Huss-Garcia Y, Duboule D (2006) A mouse model for human short-stature syndromes identifies Shox2 as an upstream regulator of Runx2 during long-bone development. Proc Natl Acad Sci USA 103:4511–4515
Vickerman L, Neufeld S, Cobb J (2011) Shox2 function couples neural, muscular and skeletal development in the proximal forelimb. Dev Biol 350:323–336
Bobick BE, Cobb J (2012) Shox2 regulates progression through chondrogenesis in the mouse proximal limb. J Cell Sci 125:6071–6083
Yu L, Gu S, Alappat S, Song Y, Yan M, Zhang X et al (2005) Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate. Development 132:4397–4406
Gu S, Wei N, Yu L, Fei J, Chen Y (2008) Shox2-deficiency leads to dysplasia and ankylosis of the temporomandibular joint in mice. Mech Dev 125:729–742
Blaschke RJ, Hahurij ND, Kuijper S, Just S, Wisse LJ, Deissler K et al (2007) Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development. Circulation 115:1830–1838
Espinoza-Lewis RA, Yu L, He F, Liu H, Tang R, Shi J et al (2009) Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nk2-5. Dev Biol 327:376–385
Scott A, Hasegawa H, Sakurai K, Yaron A, Cobb J, Wang F (2011) Transcription factor short stature homeobox 2 is required for proper development of tropomyosin-related kinase B-expressing mechanosensory neurons. J Neurosci 31:6741–6749
Rosin JM, McAllister BB, Dyck RH, Percival CJ, Kurrasch DM, Cobb J (2015) Mice lacking the transcription factor SHOX2 display impaired cerebellar development and deficits in motor coordination. Dev Biol 399:54–67
Hoffmann S, Berger IM, Glaser A, Bacon C, Li L, Gretz N et al (2013) Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia. Basic Res Cardiol 108:339
Tronche F, Kellendonk C, Kretz O, Gass P, Anlag K, Orban PC et al (1999) Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety. Nat Genet 23:99–103
Tvrdik P, Capecchi MR (2006) Reversal of Hox1 gene subfunctionalization in the mouse. Dev Cell 11:239–250
Rosin JM, Abassah-Oppong S, Cobb J (2013) Comparative transgenic analysis of enhancers from the human SHOX and mouse Shox2 genomic regions. Hum Mol Genet 22:3063–3076
Dykes IM, Tempest L, Lee SI, Turner EE (2011) Brn3a and Islet1 act epistatically to regulate the gene expression program of sensory differentiation. J Neurosci 31:9789–9799
Geisen MJ, Di Meglio T, Pasqualetti M, Ducret S, Brunet JF, Chedotal A et al (2008) Hox paralog group 2 genes control the migration of mouse pontine neurons through slit-robo signaling. PLoS Biol 6:e142
Goddard JM, Rossel M, Manley NR, Capecchi MR (1996) Mice with targeted disruption of Hoxb-1 fail to form the motor nucleus of the VIIth nerve. Development 122:3217–3228
Susulic VS, Frederich RC, Lawitts J, Tozzo E, Kahn BB, Harper ME et al (1995) Targeted disruption of the beta 3-adrenergic receptor gene. J Biol Chem 270:29483–29492
Brinster RL, Braun RE, Lo D, Avarbock MR, Oram F, Palmiter RD (1989) Targeted correction of a major histocompatibility class II E alpha gene by DNA microinjected into mouse eggs. Proc Natl Acad Sci USA 86:7087–7091
Nagy A, Gertsenstein M, Vintersten K, Behringer RR (2003) Manipulating the mouse embryo: a laboratory manual, 3rd edn. Cold Spring Harbor Press, New York
Cobb J, Duboule D (2005) Comparative analysis of genes downstream of the Hoxd cluster in developing digits and external genitalia. Development 132:3055–3067
Echelard Y, Epstein DJ, St-Jacques B, Shen L, Mohler J, McMahon JA et al (1993) Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity. Cell 75:1417–1430
Dodd J, Morton SB, Karagogeos D, Yamamoto M, Jessell TM (1988) Spatial regulation of axonal glycoprotein expression on subsets of embryonic spinal neurons. Neuron 1:105–116
JMR, DMK and JC conceived and designed the experiments. JMR performed the experiments and prepared the manuscript. JMR, DMK and JC edited the manuscript. All authors read and approved the final manuscript.
The authors thank C. Schuurmans and N. Klenin for the α-Caspase3 antibody, S. Neufeld for the Ptch1 in situ probe, S. Abassah-Oppong and I. Skuplik for BAC RP23-105B3-lacZ mice and embryos, B. Bobick for Wnt1Cre; Shox2 +/− animals and assistance during the analysis of the Shox2 lacZ transgenic line, S. Pattar and C. Ostler for their contributions to the analysis of the Shox2 lacZ transgenic line, R. Hampton for animal care, and D. Hansen, E. Turner and T. Cox for critical discussion. J.C is supported as an Alberta Heritage Foundation for Medical Research (AHFMR) Scholar. J.M.R. is supported by fellowships from NSERC and the CIHR Training Program in Genetics, Child Development and Health at the University of Calgary. D.M.K is supported by the Canadian Institute of Health Research (CIHR). This work was supported by the Canadian Institute of Health Research (CIHR) (MOP-93562).
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.
Deborah M Kurrasch and John Cobb contributed equally to this work
Figure S1. Shox2 lacZ transgenic analysis. (A) Schematic of the 15.4 kb Shox2-LacZ transgene (above) and the endogenous Shox2 genomic locus (below). The five exons are shown as vertical boxes; red indicates the coding portion of the exons and unfilled regions indicate the untranslated regions (UTRs). Green boxes/arrows indicate the sequences and sizes (in basepairs) amplified by PCR in panels B and C. The 5,200 bp PCR product amplified from genomic DNA of Shox2 lacZ mice (panel B) provides evidence for targeting via homologous recombination at the 5′ end of the gene (dotted lines). The forward primer for this PCR is 327 bp upstream of the transgene sequence and the reverse primer is within the lacZ cassette (blue). The 3′ insertion site has not yet been characterized. (B) Long range PCR demonstrating location of the transgene at the Shox2 locus, as shown by the 5.2 kb PCR product in five mice carrying the transgene but not in wild-type controls. (C) Genotyping of Shox2 lacZ mice. The wild-type allele is indicated by the 705 bp band and the transgene insertion is detected by the 392 band, with both bands amplified in heterozygote animals. The two lanes at right have only the lower band, indicating that homozygous Shox2 lacz/lacZ mice do not have an intact exon 1 in their genomes, which further supports targeting at the Shox2 locus. (D) WISH for Shox2 at E12.5. (D’-D’’’) ISH for Shox2 on E12.5 brain sections. (E) X-gal staining of an E12.5 Shox2 lacZ/+ embryo and corresponding brain sections (E’-E’’’). D’ and E’ are located anterior to D’’’ and E’’’. (F-I) Forelimb (F, G) and hindlimb (H, I) skeletons of newborn Shox2 lacZ/− mice (G, I) and controls (F, H) showing reduction in the humerus (h) and femur (f) as those found in Shox2-null mice. (J, K) Hematoxylin and eosin (H&E) stained coronal sections through the palate of newborn Shox2 lacZ/− mice (K) and controls (J) displays a cleft palate (compare J to K, dashed-box and arrow) similar to what is found in Shox2-null mice. Abbreviations: ey, eye; tg, trigeminal; di, diencephalon; mes, mesencephalon; hb, hindbrain; drg, dorsal root ganglia; nt, neural tube; fl, forelimb; hl, hindlimb; sc, scapula; r, radius; u, ulna; a, autopod; pg, pelvic girdle; t, tibia; fi, fibula; PS, palate shelf
Figure S2. Conditional removal of Shox2 using Nestin-Cre does not result in disruptions to the migratory programs of vMNs. (A) Diagram of a transverse section through rhombomere 4 (r4) of the E11 brain highlights progenitors (red arrow, known to be Phox2b + ) and post-mitotic neurons (black arrow, region known to be Phox2b +/Isl1 + ) adjacent to the floor plate (fp) (image adapted from Pattyn et al. ). (B) ISH for Shox2 on an E11 transverse brain section through rhombomere 4 shows Shox2 expression in post-mitotic neurons (black arrow) but not in progenitors (red arrow). (C-E) ISH images from the Allen Brain Atlas database (http://www.brain-map.org) show Shox2 (C, http://developingmouse.brainmap.org/experiment/siv?i100082467&imageId = 101400047&initImage = ish), Isl1 (D, http://developingmouse.brain-map.org/experiment/siv?id = 100029096&imageId = 100647957&initImage = ish) and Phox2b (E, http://developingmouse.brain-map.org/experiment/siv?id=100077806&imageId=101287085&initImage=ish) expression in vMNs in sagittal sections at E11.5 (red arrows point to Phox2b + vMNs adjacent to the ventricular zone). (F-K) ISH on E11.5 serial sagittal sections through the hindbrain of control (F, H, J) and Nestin-Cre; Shox2 flox/− mutant (G, I, K) embryos shows loss of Shox2 expression in the brain (compare F to G, arrows), while Isl1 (compare H to I, arrows) and Phox2b (compare J to K, arrows) expression is maintained in neurons migrating from the approximate rhombomere 4/5 (r4/r5) boundary to rhombomere 6 (r6), depicted using a red-dashed line. (L) Image of an E11.5 hindbrain sagittal section available from the Allen Brain Atlas database (http://atlas.brain-map.org/atlas?atlas=181275741#atlas= 181275741&plate = 100425904&structure = 126651910&x = 5432&y = 2371&zoom = -2&resolution = 3.96&z = 6) indicates rhombomere divisions (r2 to r7) within the pontomedullary hindbrain (PMH). (M-R) ISH on E12.5 serial sagittal sections through the hindbrain of control (M, O, Q) and Nestin-Cre; Shox2 flox/− mutant (N, P, R) embryos shows loss of Shox2 expression in the brain (compare M to N, arrow), while Isl1 (compare O to P, arrow) and Phox2b (compare Q to R, arrow) expression remain (approximate r5/6 boundary depicted using a red-dashed line). (S) Image of an E13.5 hindbrain sagittal section available from the Allen Brain Atlas database (http://atlas.brainmap.org/atlas?atlas=181276130#atlas = 181276130&plate = 100793031&structure = 111220768&x = 4931&y = 2197&zoom = -2&resolution = 3.96&z = 6) indicates rhombomere divisions (r5 to r7). Scale bar = 500 μm
Figure S3. Conditional removal of Shox2 using Nestin-Cre does not result in disruptions in palate development. (A, B) WISH on E12.5 control (A) and Nestin-Cre; Shox2 flox/− mutant (B) embryos shows loss of Shox2 expression in parts of the developing trigeminal (V) ganglion (arrow), in addition to the developing maxillary process (mp, arrow) and mandibular arch (ma, arrow) in Nestin-Cre; Shox2 flox/− mutants as compared to controls. (C, D) ISH on E12.5 sagittal sections through the hindbrain of control (C) and Nestin-Cre; Shox2 flox/− mutant (D) embryos shows loss of Shox2 expression in the brain, including the facial motor nucleus (nVII, dashed-circle). (E) Representative image of P0 control (left) and Nestin-Cre; Shox2 flox/− mutant (right) pups shows Nestin-Cre; Shox2 flox/− animals with less milk in their stomachs as compared to controls (red arrows). (F-I) Coronal sections through the palate of control (F, H) and Nestin-Cre; Shox2 flox/− (G, I) pups demonstrate that Nestin-Cre; Shox2 flox/− animals have an intact palate (compare F to G and H to I, arrows). F and G are rostral sections, while H and I are more caudal sections through the palate. (J, K) Representative P0 control (J) and Nestin-Cre; Shox2 flox/− (K) pup palates (viewed ventrally) show that Nestin-Cre; Shox2 flox/− mutant animals have an intact palate. Abbreviations: ey, eye; cb, cerebellum; PS, palate shelf; PP. Scale bar = 500 μm
Movie 1. Representative video of a P0 control and Nestin-Cre; Shox2 flox/− mutant pup. This video highlights the different levels of physical activity of NestinCre-Cre; Shox2 flox/− mutant pups (which are less active and display tremors) as compared to control pups, in addition to demonstrating that NestinCre-Cre; Shox2 flox/− mutant pups have very little milk in their stomachs as compared to controls
Figure S4. Conditional removal of Shox2 using Wnt1-Cre does not influence axonal projection properties of vMNs. (A, B) WISH on E12.5 control (A) and Wnt1-Cre; Shox2 flox/− mutant (B) embryos show loss of Shox2 expression in the developing trigeminal (V) ganglion, in addition to the developing maxillary process (mp) and mandibular arch (ma). (C, D) Side view of the E12.5 face of control (A) and Wnt1-Cre; Shox2 flox/− mutant (B) embryos stained with the 2H3 anti-neurofilament antibody show intact facial nerves (VII). Abbreviations: ey, eye. Scale bar = 500 μm
About this article
- Short stature homeobox 2 (Shox2) gene
- Islet 1 (Isl1)
- Sonic hedgehog (Shh)
- Visceral motor neurons (vMNs)
- Facial motor nucleus
- Facial (VII) nerves