The planar polarity of vestibular hair cells in the utricle and saccule of the mouse inner ear is established by the overlapping function of the core PCP proteins which coordinate stereociliary bundle orientation along a shared polarity axis, and the transcription factor EMX2 which determines the orientation of the stereociliary bundle relative to that PCP polarity axis (Deans, 2021; Jiang et al., 2017). EMX2 expression is restricted to the lateral region of the utricular sensory epithelium and the inner region of the saccular sensory epithelium, and the hair cells in these regions orient their bundles such that the kinocilium is positioned adjacent to the PCP protein PK2, and opposite of Frizzled. In contrast, the kinocilium in EMX2-negative hair cells of the other regions are positioned opposite of PK2 and therefore adjacent to Frizzled (Deans, 2021; Deans et al., 2007; Jiang et al., 2017). As a result, the vestibular maculae contain two groups of hair cells with opposite bundle orientations that meet at the LPR (Figure 1A–D). EMX2 directly regulates bundle orientation relative to the underlying PCP axis because all utricular hair cells adopt the orientation of medial hair cells in Emx2 mutant mice and the orientation of lateral hair cells following EMX2 overexpression (Jiang et al., 2017). Genes regulated by EMX2 during vestibular development in the mouse were identified using a bulk RNAseq approach in which the transcriptional profile of Emx2 mutant utricles was compared to utricles dissected from wild type littermate controls (Figure 1H). Mutants were derived from the Emx2-Cre knock-in line in which the Emx2 coding sequence is replaced by Cre recombinase (Kimura et al., 2005). In these Emx2 ^Cre/Cre mice, EMX2 function is lost and all utricular hair cells are oriented in a common direction (Figure 1E–G) similar to that originally reported in Emx2 knockout (KO) mice (Holley et al., 2010).

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RNAseq revealed significant changes in gene expression in Emx2 ^Cre/Cre utricles that included the downregulation of genes that are presumed to be direct or indirect transcriptional targets of EMX2 (Supplementary file 1). Despite this, the majority of genes with statistically significant changes in expression levels were still present and did not have changes in their spatial distribution in Emx2 ^Cre/Cre utricles when compared to controls by in situ hybridization techniques. Nonetheless, several genes that were downregulated or missing included Slc26a4, Caln1 and Stk26/Mst1 (Figure 1—figure supplement 1 1). These genes are found in the transitional epithelium, an EMX2-expressing region adjacent to the sensory epithelia that does not contain hair cells but may contain hair cell progenitors (Burns et al., 2015; Jan et al., 2021) and contributes to maintaining the ionic composition of endolymph (Kim and Marcus, 2011). Since these genes are not found in utricular hair cells, they are not likely to encode regulators of bundle orientation.

Genes that show increased expression in Emx2 ^Cre/Cre utricles are likely to be transcriptionally repressed by EMX2, through either direct or indirect mechanisms, and may also contribute to hair cell patterning about the LPR (Supplementary file 2). One such candidate was Stk32a/Yank1 which is expressed in the medial region of the utricle and outer region of the saccule in a pattern complementary to that of Emx2 when visualized by fluorescent in situ hybridization (fISH) (Figure 1I and J). STK32A is a serine threonine kinase with sequence similarity to AGC kinases and is a member of a small kinase protein family that includes STK32B/YANK2 and STK32C/YANK3. The STK32 kinases have been categorized as dark kinases because their substrates and biological functions are not known (Berginski et al., 2021). Within the developing utricle, Stk32a mRNA was detected in clusters that overlapped with mRNA transcribed from the hair cell gene Gfi1 (Figure 1K). A similar pattern of expression was seen in the semi-circular canal cristae (Figure 1L and M). The hair cells in each of these regions lack EMX2 and have stereociliary bundles oriented with the kinocilium positioned opposite of PK2 similar to utricular hair cells located medial to the LPR (Deans et al., 2007).

The increase in Stk32a mRNA detected by RNAseq is due to an expansion of the Stk32a expression domain and in the absence of Emx2, Stk32a mRNA can be detected throughout the entire sensory epithelia (Figure 2A and B). This expansion was quantified from multiple biological replicates by measuring the ratio of average fluorescence intensities of fISH signal for Stk32a mRNA in medial versus lateral regions. When expressed as a ratio, medial Stk32a expression is more than 3-fold higher in littermate controls than in Emx2 ^Cre/Cre utricles where this ratio becomes equally proportioned due to Stk32a expansion (Figure 2D, E and H). Conversely, when Emx2 is ectopically expressed in hair cells throughout the sensory epithelia using hair cell-restricted Gfi1-Cre crossed with Lox-Stop-Lox (LSL) Emx2 overexpression mice (Rosa26 ^LSL-Emx2), Stk32a expression is reduced wherever Emx2 is induced (Jiang et al., 2017). As a result, the expression of both genes becomes balanced between the medial and lateral utricle with fluorescent expression ratios that are equally proportioned (Figure 2F, G, I, J). Together these gene expression studies identify Stk32a as a gene negatively regulated in the lateral region of the utricle resulting in non-overlapping and complementary patterns of Emx2 and Stk32a.

Figure 2

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As Stk32a is negatively regulated by EMX2, STK32A function in planar polarity was evaluated using an adeno-associated virus (AAV) vector to overexpress Stk32a mRNA in lateral hair cells of the utricle where Stk32a expression is normally repressed. For these experiments, utricles were micro-dissected and grown as explants prior to AAV transduction. Since the AAV vector does not contain the genomic regulatory elements surrounding Stk32a it is not subject to EMX2 associated repression. Transduced cells were identified based upon EGFP expression from a bicstronic Stk32a-P2A-EGFP mRNA (Figure 3B–E). Following 48 hr in culture post-transduction, bundle orientation was determined using βII-Spectrin immunolabeling of the cuticular plate to visualize the fonticulus and thereby infer the position of the kinocilium and orientation of the bundle. Since culture conditions often distorted explant growth, coarse measures of bundle orientations were used that defined medial and lateral orientations based upon position of the fonticulus within quadrants on the medial or lateral apical cell surface (Figure 3F). Hair cells with a fonticulus located in one of the two remaining quadrants of the cell surface were grouped as misoriented. βII-SPECTRIN labeling in some cells did not provide a defined fonticulus that could be used to evaluate orientation and were grouped as undetermined. Control explants were transduced with AAV expressing EGFP alone and the majority of transduced cells had bundle orientations appropriate for their position in the medial or lateral utricle (Figure 3A,A’,F).

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In contrast to controls, hair cells located in the lateral utricle transduced at P0 with AAVs expressing Stk32a-P2A-EGFP showed prominent changes in bundle orientation with many lateral hair cells having orientations that resembled hair cells from the medial utricle (Figure 3B,B’,F). A smaller proportion were also misoriented relative to non-transduced neighbors though it could not be determined whether this was their final orientation or whether they were undergoing an STK32A-mediated rotation at the time of tissue fixation. When lateral hair cells were transduced at P5 with Stk32a-P2A-EGFP (Figure 3E,E’,F), fewer reversed cells were present suggesting that the impact of ectopic STK32A might be age dependent. Most likely this is because STK32A acts during stereociliary bundle morphogenesis and is less capable of reorienting the bundle once the structure has matured. This effect is also likely dependent upon the kinase activity of STK32A because it is disrupted by substituting the Lysine residue that facilitates ATP-binding prior to substrate phosphorylation with Arginine (K52R) (Sorrell et al., 2020; UniProt Consortium, 2021). Consistent with this, AAV expressing Stk32 ^K52R-P2A-EGFP was incapable of reorienting hair cells in the lateral region of the utricle when introduced to utricle explants at P0 (Figure 3C,C’,F).

Currently available antibodies against STK32A lack the specificity to distinguish STK32A from the closely related STK32B and STK32C kinases and demonstrate poor labeling of fixed tissues (data not shown). Therefore, in order to determine the sub-cellular distribution of STK32A, Stk32a::EGFP fusion constructs were generated and transduced into developing hair cells using AAV vectors. Since EGFP-tag placement may impact protein localization, alternative viruses expressing Amino- and Carboxy-terminal EGFP were evaluated. Carboxy-terminal EGFP tag had a greater capacity to promote reversed bundle orientations in lateral hair cells (Figure 3—figure supplement 1). Since STK32A::EGFP appeared functional in this assay, the distribution of EGFP immunolabeling was used as a proxy for the subcellular distribution of endogenous STK32A. Using this approach, STK32A::EGFP was detected in the apical compartment of transduced hair cells and stereociliary bundle (Figure 3G, H). STK32A::EGFP can be detected in this apical compartment between 12 hr and 24 hr post-transduction and continues to be enriched in this area despite increased STK32A::EGFP labeling throughout the hair cell over the subsequent 48 hr. This is in contrast to EGFP alone which remained cytosolic and strictly labeled the cell soma (Figure 3A–E). Motif-based evaluation of the STK32A primary amino acid sequence also identified the potential for myristoylation of the Glycine located at amino acid position 2. The potential for this lipid modification to localize STK32A to the apical compartment of hair cells was tested using AAV expressing a GFP fusion protein in which the N-myristoyl glycine is deleted. When evaluated in transduced hair cells STK32A^Δ2G::EGFP was not enriched in the stereociliary bundle (Figure 3F,I,I’,J,J’). Moreover, STK32A^Δ2G::EGFP was not capable of reversing the orientation of hair cells in the lateral utricle indicating that STK32A needs to be located at the apical cell surface to have this affect (Figure 3D, D’ and F). Together, the distribution of these STK32A::EGFP fusion proteins and the capability of STK32A::EGFP to generate hair cells with medial bundle orientations in the lateral utricle suggests that endogenous STK32A functions in the apical compartment of developing hair cells.

Since STK32A is sufficient to direct lateral hair cells of the utricle to develop reversed bundle orientations, a knockout (KO) mouse was generated using CRISPR-mediated mutagenesis to determine if Stk32a was also necessary for the planar polarized development of medial hair cells (Figure 4—figure supplement 1). This targeting strategy generated two CRISPR-mediated DNA breaks in the introns flanking Stk32a exon 2, which contains the translational start and N-myristoyl glycine, and deleted exon 2 following non-homologous end-joining repair. The lack of a suitable antibody against STK32A prevented Western blot analyses to determine whether a mutant protein was translated from alternative start codons. However, any mutant protein would lack the essential N-myristoyl glycine and ATP-binding motifs required for function. When the deletion was homozygosed, Stk32a ^-/- mice were viable, survived to adulthood and showed no overt physical or behavioral differences from littermate controls. Furthermore, no differences were detected in the planar polarized organization of utricular hair cells between wild type and Stk32a ^+/- littermates (Figure 4—figure supplements 2–3). Since this indicated that exon2 deletion did not result in a dominant-negative or hypomorphic allele, heterozygotes were used as controls for all subsequent analyses.

When evaluated by immunofluorescent labeling of βII-SPECTRIN at P5, it was evident that the planar polarized organization of vestibular hair cells in the medial regions of the Stk32a ^-/- utricle was severely disrupted (Figure 4 and Figure 4—figure supplement 2). Unexpectedly, mutant hair cells in these regions did not assume the same bundle orientation of hair cells that do not normally express Stk32a located in the lateral region. Instead the bundles of hair cells in the striolar and medial extrastriolar regions of the Stk32a ^-/- utricle were randomly oriented relative to each other (Figure 4E–L) while lateral hair cells remained correctly oriented (Figure 4A–D). Misoriented bundles were also seen in the outer region of the saccule (Figure 4M–P) and within the semi-circular canal cristae (Figure 4Q-Bb); regions that normally express Stk32a and not Emx2. Cumulative measures of bundle orientation plotted as circular histograms confirmed this phenotype across biological replicates and demonstrated that bundle orientation was disorganized rather than reversed (Figure 4). The location of analysis fields used for these measures relative to domains of Emx2 and Stk32a expression are summarized schematically (Figure 4—figure supplement 2). In general, the extent of misorientation was greater in the maculae than in the cristae though the basis for this difference is unknown. Auditory hair cells were not impacted in Stk32a ^-/- cochleae (Figure 4—figure supplement 4), most likely because they express Emx2 and not Stk32a (Jiang et al., 2017; Orvis et al., 2021). Despite the randomization phenotype, the intrinsic polarity of the majority of vestibular hair cells remained intact with kinocilium that were located on one side of the apical cell surface adjacent to the tallest row of stereocilia (Figure 5A–B).

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Figure 5

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This Stk32a ^-/- phenotype resembles that of PCP mutants in which hair cells are also misoriented relative to their neighbors (Stoller et al., 2018; Yin et al., 2012). However, immunofluorescent labeling of core PCP proteins suggests that PCP signaling remains intact in Stk32a ^-/- sensory epithelia. For example PK2, which is asymmetrically distributed along one side of the hair cell (Deans et al., 2007), remains normally distributed in Stk32a ^-/- hair cells (Figure 5C–D). As a result, in some Stk32a ^-/- hair cells, PK2 can be found on the side of the bundle rather than adjacent to or opposite of the kinocilium as seen in controls. In addition, the polarized distribution of CELSR1 at junctions between supporting cells is not altered in Stk32a ^-/- (Figure 5E, F). Emx2 expression in the lateral extrastriolar region of the utricle and adjacent transitional epithelia was also not impacted by Stk32a gene deletion (Figure 5G and H) consistent with this transcription factor acting upstream of Stk32a expression. Together these observations demonstrate an STK32A function in the medial utricle that coordinates intrinsic polarity of the hair cells with the PCP axis, and that is inhibited in the lateral utricle by EMX2.

In the lateral region of the utricle and inner region of the saccule, EMX2 acts upstream of the G-protein-coupled receptor GPR156 to reorient stereociliary bundles and thereby position the LPR (Kindt et al., 2021). Remarkably, GPR156 function is regulated post-translationally because it is expressed by all vestibular hair cells, but can only be detected at the apical hair cell surface in hair cells that also express Emx2. The mechanisms regulating GPR156 distribution at the cell surface are not known, although it seems likely that factors transcriptionally regulated by EMX2 contribute to this process.

The potential for STK32A to regulate GPR156 distribution at the apical surface of hair cells was tested by visualizing GPR156 protein in the Stk32a ^-/- maculae and semi-circular canal cristae (Figure 6). For these experiments, Pericentrin immunolabeling was used to mark the basal body and determine hair cell orientation. In controls, GPR156 was polarized apically in hair cells of the lateral utricle and inner saccule (Emx2-positive domains), but not in the rest of the organs (Emx2-negative domains), as reported previously (Figure 6A and C). In Stk32a ^-/-, however, GPR156 was also detected apically in the Emx2-negative domains of the utricle (Figure 6B) and saccule (Figure 6D). Similarly, GPR156 was detected at the cell boundary in Stk32a ^-/- cristae, but not in control cristae as expected (Figure 6E and F and Kindt et al., 2021). Despite ectopic localization at apical cell boundaries in Emx2-negative hair cells, GPR156 was not tightly polarized as seen in control utricular cells on the lateral side of the LPR, and was either symmetrical and surrounded individual cells, or was polarized but imprecisely aligned with the PCP axis (Figure 6B’’, D’’ and F’’).

Figure 6

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To directly test whether STK32A negatively regulates GPR156 delivery to or retention at the cell surface, Stk32a-P2A-EGFP plasmids were electroporated into auditory hair cells at E13.5 and the cochlea cultured for an additional week (Figure 7). Auditory hair cells were selected for experimentation because plasmid electroporation is more efficient and GPR156 enrichment is easier to detect than for vestibular hair cells (Kindt et al., 2021). Stk32a is also not normally expressed in the auditory epithelium. Individual hair cells ectopically expressing Stk32a had decreased levels of GPR156 or displayed no GPR156 protein at their apical cell surface (Figure 7A, A’, B and B’). This reduction was quantified by calculating a ratio of GPR156 enrichment at the medial cell boundary of electroporated versus non-electroporated neighbors for Egfp control and Stk32a constructs (Figure 7E). In addition to changes in GPR156, a subset of Stk32a-P2A-EGFP expressing hair cells (8 of 50) also had an inverted intrinsic planar polarity that was revealed by changes in the distribution of aPKC (Figure 7C and C’). In contrast, auditory hair cells electroporated with constructs expressing the predicted kinase-dead Stk32a ^K52R mutant continued to display GPR156 protein at their apical cell boundaries (Figure 7D and D’) suggesting that STK32A kinase activity is required for the negative regulation of GPR156 distribution. Notably, the asymmetric distribution of GPR156 was also impacted by the Stk32a ^K52R mutation because GPR156 could be detected at both the medial and lateral cell boundaries (Figure 7D and F). While the molecular basis of this change is not known, it is possible that physical interactions between STK32A and GPR156 underlie the redistribution of GPR156 following the overexpression of STK32A ^K52R throughout the hair cell. Altogether, these gene deletion and electroporation-mediated overexpression assays demonstrate that STK32A is required for the post-translational regulation of GPR156 function through a phosphorylation-dependent event that regulates the presence of this receptor at the apical hair cell surface.

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We have identified the serine-threonine kinase STK32A as a planar polarity factor that functions opposite of EMX2 and provide genetic evidence that STK32A is necessary and sufficient to determine the orientation of mouse vestibular hair cells. Stk32a transcription is repressed in the lateral utricle and inner region of the saccule and in the absence of Emx2, Stk32a expression is expanded to include all hair cells in those regions. This expansion likely explains how in the Emx2 mutant, lateral hair cells in the utricle remain uniformly oriented along the PCP axis albeit with bundle orientations characteristic of medial hair cells (Jiang et al., 2017). We further demonstrate that in the absence of Stk32a, medial hair cells are randomly oriented and no longer aligned with the underlying PCP axis. Finally, we demonstrate that STK32A contributes to LPR formation by regulating the sub-cellular distribution of GPR156 so that it is only present at the apical boundaries of hair cells where EMX2 is expressed and Stk32a transcription is repressed. Based upon these observations we propose the following model for how STK32A functions together with EMX2 and GPR156 to pattern hair cells about the LPR (Figure 8). In this model, GPR156 functions at the apical cell boundaries to align stereociliary bundles with the underlying PCP axis so that the basal body is positioned adjacent to PK2 in EMX2-positive regions of the utricle and saccule (Jiang et al., 2017; Kindt et al., 2021). STK32A serves a similar function in EMX2-negative regions by positioning the basal body opposite of PK2 though the targets of STK32A kinase activity at this step remain unknown. The LPR is formed along the boundary of Emx2 expression and is maintained by hair cells through two steps of negative regulation. In the first, STK32A inhibits GPR156 delivery or retention at the apical boundary of cells located on the medial, EMX2-negative side of the LPR. In the second, EMX2 represses Stk32a transcription in those hair cells located on the EMX2-positive side of the LPR, allowing GPR156 to accumulate at the cell surface where it can promote Emx2-dependent bundle reversal. An essential tenet of this model is that intercellular PCP signaling functions solely to align neighboring cells along a common polarity axis and is not impacted by Emx2, Gpr156 or Stk32a mutations as has been shown previously (Jiang et al., 2017; Kindt et al., 2021 and Figure 5). In this model, the final position of the basal body and kinocilium relative to the core PCP proteins are determined by STK32A or GPR156.

Figure 8

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Yet to be determined is whether EMX2 acts directly as a transcriptional repressor that binds the Stk32a promoter or indirectly through intermediary factor(s) to regulate Stk32a expression. Prior transcriptional profiling has shown that EMX2 contributes to both transcriptional activation and repression in the developing telencephalon prior to cortical arealization (Hamasaki et al., 2004; Li et al., 2006), but these studies also did not distinguish between direct or indirect mechanisms. DNA binding assays have shown that EMX2 is capable of occupying POU sites in the Sox2 enhancer and repressing Sox2 expression in a dose-dependent manner (Mariani et al., 2012). The positive and negative regulation of gene expression may also be determined by cofactors since EMX2 represses Gsx2 gene expression during earlier stages of telecephalic development but only in the presence of DMRT3 and DMRT5 (Desmaris et al., 2018). Overall the precedent set by these prior studies of telencephalic and cortical development is consistent with our interpretation and that EMX2 contributes to transcriptional repression in the vestibular sensory organs. Moreover, they highlight the diversity of mechanisms that might mediate this effect including the potential for additional unidentified intermediaries or co-factors specific to vestibular hair cells.

Based upon our analysis of Stk32a knockouts one possibility could be that that STK32A has two functions during vestibular hair cell development. The appearance of randomly oriented bundles in the medial region of the mutant utricle and outer region of the saccule suggests that one function is to align bundle orientation with the PCP axis. Thus, in Stk32a ^-/- hair cells the basal body either moves incorrectly relative to the PCP axis or is not maintained in a fixed position following an initially correct movement. A second function is revealed by the ectopic overexpression of STK32A in cochlear hair cells where the apical distribution of GPR156 is similar to EMX2-positive vestibular hair cells. Although not normally expressed in these cells, the addition of STK32A dramatically reduces that amount of GPR156 detected at apical cell boundaries. Together with the aberrant appearance of GPR156 at the surface of EMX2-negative vestibular hair cells in Stk32a ^-/- mice, these data demonstrate a second STK32A function in the post-translational regulation of GPR156. STK32A could do this either by regulating a key step of GPR156 trafficking and delivery to the cell surface, or by activating the internalization of GPR156 from the cell surface after delivery has occurred. It should be noted however, that the distribution the GPR156 in Stk32a ^-/- hair cells on the EMX2-negative side of the LPR does not have the same uniform planar polarized distribution that characterizes GPR156 distribution in hair cells that have EMX2. This suggests the contributions of additional, yet to be identified, factors that also regulate GPR156 localization. The disorganized distribution of GPR156 also raises an alternative possibility that STK32A only has one function during hair cell development which is to negatively regulate GPR156. In this scenario, the misoriented stereociliary bundles seen in Stk32a ^-/- would not be due to an STK32A function in regulating the position of the kinocilium. Instead the disorganization could be an artifact of GPR156 which does not normally function in these cells, is lacking a planar polarized organization, and could therefore disrupt the proper positioning of the kinocilium. This simplified role of STK32A would not disrupt the general tenets of the model we propose for EMX2, STK32A and GPR156 function (Figure 8), and in this scenario we would propose that the core PCP proteins determine the position of the kinocilium in hair cells not expressing EMX2.

A limitation to the current study is that we lack a suitable antibody for evaluating the subcellular distribution of STK32A which limits the detail of the mechanistic models that can be proposed. Predictions based on sequence analysis suggest that SKT32A is membrane-associated due to the potential for myristoylation of an N-terminal glycine (UniProt Consortium, 2021; UniProt C, 2023). Our observations that EGFP-tagged STK32A is present in stereocilia and at the apical cell surface and that this localization is lost following deletion of the N-terminal glycine, is consistent with myristoylation-dependent targeting to this location. This apical localization of STK32A would be most consistent with an STK32A function to promote the internalization of GPR156 from the apical cell boundary rather than trafficking and delivery to that location. Alternatively, STK32A has been predicted to localize to cilia (Atlas THP, 2022; Thul et al., 2017) and therefore may be aptly suited to position the kinocilium relative to the PCP axis. Consistent with this alternative, a large-scale immuno-precipitation and mass spectrometry analysis of kinase binding partners found that STK32A associated with components of the chaperonin-containing T-complex (TRiC) (Buljan et al., 2020). This complex may play a role in formation of the BBSome, a complex associated with ciliogenesis (Seo et al., 2010) that has also been associated with ciliopathies and planar cell polarity (Ross et al., 2005). A better understanding of STK32A function will occur following the identification of the phosphorylation substrates and potential binding partners for this kinase. A striking candidate is GPR156 since we show that STK32A can negatively regulate its localization to the cell surface. Despite this we have been unable to demonstrate physical interactions or phosphorylation events for these two proteins following overexpression in heterologous cell lines, raising the possibility that GPR156 regulation is indirect and requires additional, intermediary proteins also found in hair cells.

The human genome encodes over 500 kinases yet despite their identification and classification, the substrates and signaling pathways for approximately 160 of these kinases remain poorly understood (Berginski et al., 2021). These remaining enzymes have been dubbed Dark Kinases and include the small protein family of STK32A, STK32B, and STK32C. To the best of our knowledge, no prior studies have associated the STK32/YANK kinase family with hair cells, planar polarity or inner ear development. Based on sequence homology and crystal structure the STK32/YANK family is a sub-group of the ACG kinases which include the better understood PKA, PKC and PKG proteins (Sorrell et al., 2020). Although prior knowledge of STK32A is limited, it has been linked to stomach adenocarcinoma (STAD) where its overexpression is associated with lower overall survival (Southekal et al., 2021), and somatic mutations in Stk32a have also been identified in neuroendocrine carcinoma of the lung and metastatic melanoma (Greenman et al., 2007). Our analyses reveal that this kinase is a regulator of cellular polarity that aligns individual cells with the planar polarity axis found in many tissues and epithelia. This is an interesting observation because disrupted planar cell polarity signaling is also associated with cancer progression and metastasis (VanderVorst et al., 2018; Wang, 2009). An exciting prospect is that pharmacologic manipulation of STK32 family kinases function or their substrates could be developed as a treatment to slow progression. Towards this end, small molecules that bind to STK32A have been identified which may be useful for further research (Sorrell et al., 2020).

The results presented here remain consistent with EMX2 acting as a master regulator or switch controlling stereociliary bundle orientation and thereby determining the position of the LPR. However, our RNAseq analyses demonstrate that EMX2 does not establish the LPR through transcriptional activation but rather via the repression of genes such as Stk32a. Consistent with this, the genes that we identified as being positively regulated by EMX2 were predominantly expressed in the transitional epithelia rather than vestibular hair cells. Based on these findings we propose that EMX2 functions more broadly to define the regional identity of the lateral utricle, inner region of the saccule and neighboring non-sensory epithelia. As such EMX2 would sit atop a gene regulatory network that regulates multiple differentiation steps with hair cell planar polarity and patterning about the LPR just one of these events. We provide evidence that a key component enacting this EMX2 planar polarity effect in hair cells is the dark kinase STK32A.

Emx2 ^Cre/wt mice (Kimura et al., 2005) were provided by S.Aizawa (Riken Institute), maintained by backcross with B6129SF1/J females (Jax strain#101043) and Emx2 mutants generated by intercrossing Emx2 ^Cre/wt male and female mice. Tissue from Gfi1-Cre, Rosa26 ^LSL-Emx2/wt transgenic mice and Rosa26 ^LSL-Emx2/wt controls were provided by Doris Wu (NIH/NIDCD). The Stk32a KO mouse line was generated by targeting the second exon of the Stk32a gene, which contains the translational start, using CRISPR technology. Two gRNAs (5’-UAGAAAUGACCAUGGUGCAU-3’ and 5’-UACAGUGUAUCUAAGGAUAG-3’) that are complementary to intronic DNA sequences located on either side of Stk32a exon 2 were designed by the University of Utah Mutation Generation and Detection Core. These were combined with recombinant Cas9 protein for pronuclear injections into B6CBAF1/J mouse zygotes (Jax strain#100011) that were subsequently implanted into pseudo-pregnant females by University of Utah Transgenic and Gene Targeting Core. One male founder with an appropriate deletion generated by NHEJ and identified by PCR amplification followed by Sanger sequencing was selected for line expansion through backcross with B6129SF1/J females. PCR primers used for mutant genotyping are: Stk32a primer A (5’-AGTTTTCTTGATACCTGGGGATGT-‘3’) and Stk32a primer B (5’-GGATGGCAGTGATTATGAAAGTTG-3’). The Stk32a ^-/- phenotype was initially evaluated by intercrossing N2 heterozygous mice and the mutant phenotype was consistently observed when N3 and later generations were experimentally intercrossed. Experimental crosses consisted of Stk32a ^-/- males crossed with Stk32a^+/-females, and heterozygous littermates generated from these crosses were used as controls. CD1 mice were purchased from Charles River and intercrossed for utricle explant experiments. Mice were genotyped by PCR using allele specific primers. All animal work was reviewed for compliance and approved by the Animal Care and Use Committee of The University of Utah (IACUC protocol #00001498) and the Animal Care and Use Committees of The Jackson Laboratory (Animal Use Summary AUS no. 14012).

Inner ear tissues were fixed using 4% paraformaldehyde in 67 mM Sorensons’ phosphate buffer (pH 7.4) for 2 hr on ice, or using 10% trichloroacetic acid (TCA) for 10 min on ice depending upon primary antibody selections (see below). For wholemount immunofluorescent labeling, utricles and saccules were micro-dissected and detergent permeabilized using a blocking solution (5% normal donkey serum, 1% bovine serum albumin (BSA), PBS) supplemented with 0.5% Triton-X100. Primary antibodies and Phalloidin Alexa Fluor 488 (Invitrogen A12379) were diluted in blocking solution supplemented with 0.1% Tween-20 and incubated overnight at 4 °C. Tissue was washed thoroughly using PBS with 0.05% Tween-20 and incubated with species-specific Alexa-conjugated or Cy3 conjugated secondary antibodies (Jackson ImmunoResearch, 705-165-147, 705-605-147, 706-165-148, 711-165-152, 711-545-152, 711-605-152, 712-605-150), before mounting for fluorescence microscopy using Prolong Gold (ThermoFisher Scientific, P36930). Fluorescent images were acquired by structured illumination microscopy using the Zeiss Axio Imager M.2 with ApoTome.2 attachment and Axiocam 506 mono camera. Images in Figures 6 and 7 (Gpr156 experiments) were acquired using a Zeiss LSM800 confocal microscope and a 63 x NA1.4 objective. Images were processed using Zeiss Zen software and figures were prepared using with Adobe Illustrator.

Antibodies and fixatives used in this study are: Mouse anti-Acetylated Tubulin (1:250, PFA, Sigma-Aldrich T7451, RRID:AB_609894), Mouse anti-aPKC (1:100, TCA, Santa Cruz Biotechnology SC-17781), Mouse anti-βII Spectrin (1:1000, PFA or TCA, BD Biosciences 612562, RRID:AB_399853), Guinea Pig anti-CELSR1 (1:500, TCA, F.Tissir (Louvain)), Rabbit anti-GFP (1:1000, PFA, Life Technologies A11122, RRID:AB_221569), Goat anti-GPR156 (1:100, TCA, Santa Cruz Biotechnology SC-102572, RRID:AB_10839485), Rabbit anti-MST4/STK26 (1:500, PFA, Abcam Ab52491, RRID:AB_881249), Goat anti-Oncomodulin/OCN (1:250, PFA, Santa Cruz Biotechnology SC-7466, RRID:AB_2267583), Rabbit anti-pericentrin/PCNT (1:400, TCA, Biolegend PRB-432C, RRID:AB_291635), Rabbit anti-PK2 (1:200, PFA [Deans et al., 2007]), Rat anti-ZO1 (1:1000, TCA, DSHB R26.4C, RRID:AB_2205518).

Whole inner ear capsules were dissected from E18.5 mouse pups, generated by Emx2 ^Cre/wt intercross, under nuclease free conditions. The bony labyrinth was lightly perforated and ears were stored in RNAlater (ThermoFisher AM7020) at 4 C for 1 week to allow for subsequent collections and genotyping. Emx2 ^Cre/Cre and wild type samples were dissected under nuclease free conditions to isolated the utricle from surrounding mesenchyme and adjacent cristae. Four to 6 utricles were combined per genotype to constitute one biological replicate, and 4 replicates were collected for each. Tissue was transferred to 350 µl of RNeasy Lysis buffer (Qiagen 79216) Buffer RLT and lysed using the Qiagen Tissue Lyser LT at 20 Hz with one stainless steel bead for 4 min. Following centrifugation, supernatant was transferred to a clean tube and RNA isolated using the RNeasy Micro Kit (Qiagen 74004). DNA and RNA concentrations were determined using Qubit broad range DNA and RNA assay kits (Invitrogen Q32853 Q10211) and RNA quality evaluated using the Agilent 2200 TapeStation which returned RNA integrity numbers ranging from 8.3 to 9.1. Libraries were generated at the Huntsman Cancer Institute Genomic Core facility using TruSeq Stranded Total RNA Library Prep with Ribo-Zero Gold kits (Illumina 20020598) and sequenced using the Illumina NovaSeq 6000 for 25 M 2x50 bp reads per biological replicate. Significant unmapped reads were found in one WT sample which was excluded from subsequent analysis after principal component analysis revealed it to be a significant outlier. Remaining samples were compared using the Bioconductor DESeq package as well as by post hoc-analysis using Swish. Benjamini-Hirshberg false discover rate was used to normalize data across all transcripts and produce adjusted p-values for significantly downregulated or upregulated genes based on log2-fold changes compared to WT baseline transcript levels.

For wholemount fISH inner ears were fixed overnight at 4 °C using 4% paraformaldehyde prepared in phosphate buffered saline (PBS, pH 7.4) and stored as needed at –20 °C in 100% MeOH. Prior to hybridization tissue was dissected to expose sensory epithelia and rehydrated through a decreasing MeOH gradient (75%, 50%, 25%) ending in PBST (PBS with 0.1% Tween-20). fISH was completed using Hairpin Chain Reaction protocols (Choi et al., 2018). In brief, samples were digested in 30 µg/ml proteinase K for 20 min at room temperature followed by post-fixation in 4% PFA/PBS for 20 min. After rinsing with PBST, samples were equilibrated in hybridization buffer (30% formamide, 5 X sodium chloride sodium citrate (SSC), 0.9 mM citric acid (pH 6.0), 50 µg/mL heparin, 1 X Denhardt’s solution, 10% low MW dextran sulfate) at 37 °C for 30 min, then incubated in hybridization buffer containing 16 nmol mRNA-specific probes overnight at 37 °C. Excess probe were removed using 4 exchanges of probe wash buffer (30% formamide, 5XSSC, 9 mM citric acid (pH 6.0), 0.1% Tween 20, 50 µg/mL heparin) followed by2 exchanges of 5XSSCT (0.1% Tween in 5XSSC), then fluorescent signal amplification was performed by incubating samples with hairpin mixtures in amplification buffer (5XSSC, 0.1% Tween, 10% low MW dextran sulfate) overnight at room temperature. Hairpins were removed by extensively washing with 5XSSCT, and samples were transferred to glass slides and coverslipped using ProLong Gold Antifade mounting media (Invitrogen). Fluorescent images were captured by structured illumination microscopy using a Zeiss Axio Imager M.2 with ApoTome.2 attachments and an Axiocam 506 monochrome camera. HCR probes used in this study were: Caln1-B1 (Molecular Instruments PRF994), Emx2-B5 (Molecular Instruments PRA862), Gfi1-B2 (Molecular Instruments PRG075), Slc26a4-B1 (Molecular Instruments PRF991), Stk26-B1 (Molecular Instruments PRC152) and Stk32a-B1 (Molecular Instruments PRF996).

For quantification of mRNA detected by fISH (HCR v3.0) images were captured in three rectangle regions of interest (ROIs) of identical sizes were imaged with identical Z-plane depth from the lateral and medial regions of the utricle (Figure 2C) and processed as a max intensity projection using Zen software (Zeiss). Using ImageJ, the integrated density of each ROI was calculated for individual channels to quantify mRNA expression levels, and values were averaged across the three ROIs for a single biological replicate. Utricles from a minimum of three mice were analyzed for each genotype, and statistical significance was determined using student’s t-test.

To quantify GPR156 in cochlear explants, we defined a 2x0.5 µm window in Fiji and positioned it on an medial or lateral outer hair cell junctional region where GPR156 signals were the most intense in the cell. The mean grey value was measured for each electroporated cell along with two adjcent un-electroporated control cells. GPR156 enrichment was calculated as a ratio of averaged values for control cells. Statistical significance was determined using 1-way ANOVA (medial junction Figure 7E) or an unpaired Student’s t-test (lateral junction Figure 7F).

HEK293 (ATCC, CRL-1573) cells were used for AAV preparation based upon an established protocol (Challis et al., 2019). Cells were grown in Gibco DMEM GlutaMAX (ThermoFisher Scientific 10569010) supplemented with 10% FBS. Cells were transiently transfected with three plasmids using Polyethylenimine (PEI, Polysciences Inc 23966–100). These plasmids were variants of pAAV-MCS; the transgene expression vector containing the chicken β-actin/CMV hybrid promoter CAG2 followed by our gene of interest, pHELPER; which encodes adenoviral proteins necessary for AAV genome replication and pAAV-ie which contains viral replication and capsid proteins optimized for inner ear transduction (Tan et al., 2019). HEK293 cells were seeded onto 150 mm culture dishes and grown to 80% confluency before carrying out transfection. Cells were transfected with 40 µg total DNA per 150 mm dish and the plasmid mixture was a ratio of 1:4:2 (pAAV-MCS:pAAVie:pHELPER). Culture media containing shed AAV was harvested 72 hr and 120 hr post transfection. The AAV particles were precipitated from the media by using Polyethylene Glycol (PEG, Sigma-Aldrich P2139). At 120 hr, cells were also harvested using a cell scraper and lysed with HL-SAN salt-active nuclease (ArticZymes 70910202) to release viral particles. Cell lysates and the PEG-precipitated virus were combined and AAV was purified on an Iodixanol (OptiPrep, Serumwerk Bernburg 1893) density gradient comprised of four layers (15%, 25%, 40%, and 60%). The combined lysate was loaded on top and then ultracentrifuged at 250,000xg for 3 hours at 18 C. After the centrifugation, the 40% layer containing AAV was collected, mixed with DPBS, and filtered through a 0.22 um syringe filter unit. Residual iodixanol was removed by washing with DPBS containing 0.001% pluronic F-68 and concentrating using 100 kDa MWCO centrifugal filter units (Millipore UFC910024). Purified virus was aliquoted and stored at –80 °C. Virus titer was determined by qPCR using SYBR Green and StepOnePlus (AppliedBiosystems) quantitative PCR machine as described (Aurnhammer et al., 2012). Variants of the pAAV plasmids used contain the CAG2 promoter followed by the coding sequence of gene(s) to be overexpressed. Each was sequence verified following construction.

Utricles were dissected from the inner ears of P0 CD1 mouse pups in pre-chilled dissection solution (DPBS supplemented with 10% FBS, 0.1X N2 Supplement ThermoFisher 17502048) and 10 µg/ml Ciprofloxacin (SigmaAldrich 17850), transferred to 100 µl culture media (DMEM/F12 1:1 (ThermoFisher Cat 11330032) with 10% FBS, 0.1X N2 Supplement and 10 µg/ml Ciprofloxacin), and attached to a sterilized coverslip using Cell-Tak Cell and Tissue Adhesive (Corning 354240). Coverslips were placed into individual wells of a six-well plate and transduced with AAV premixed in culture media with AAV at (6X10⁷ virions per µl) and incubated in a cell culture incubator at 37 °C for 4 hr. After the incubation, 2–3 ml fresh culture medium was added to each well and the explant was cultured for 3 days, with fresh media added after 48 hr. Following culture, explants were washed with PBS, then fixed for 30 min with 4% PFA/PBS on ice. After fixation and brief PBS wash, coverslips were superglued onto glass microscope slides with the explant facing up and processed for wholemount immunolabeling as described previously. Following labeling explants were coverslipped using Prolong Gold Antifade mounting media with the explant was sandwiched between the two glass coverslips and the bottom most coverslip superglued to the glass slide.

Inner ears from wild-type animals (C57BL/6J x FVB/NJ) were collected at E13.5 in HBSS +5 mM Hepes buffer (14065–056 and 15630–080, respectively, Gibco). Plasmid DNA was mixed with Fast Green FCF (final 0.05%; F7252, Sigma) and injected at 2 µg/µl into the cochlear duct using the Wiretroll plunger system (53507–426, Drummond). Next, the whole inner ear was electroporated (27  V, 27ms, 6 square pulses at 950ms intervals; BTX ECM 830), and the membranous labyrinth was dissected away from the condensed mesenchyme and embedded in Matrigel (8 µl drop of 50% Matrigel in DMEM; CB40234, Corning). The explants were cultured for 6 days in DMEM with 10% fetal bovine serum and 10 µg/ml ciprofloxacin (17850, Sigma), and then fixed in 10% TCA for 10 min on ice before being processed for immunolabeling.

To evaluate bundle orientation, utricles, saccules, and cristae were immunolabeled with antibodies against βII-SPECTRIN (1:1000; BD Biosciences 612562) and Oncomodulin/OCN (1:250; Santa Cruz Biotechnology SC-7466) as described above. Orientation was determined based on the polarized position of the fonticulus and measurements aided with a customized Python script (Duncan et al., 2017) that allowed orientations to be measured relative to a user-defined reference-line. The position of analysis fields for each sensory epithelia are defined in Figure 4—figure supplement 2. For the lateral utricle, the reference line was drawn along the utricle boundary while for medial striolar and MES regions the reference line was drawn along the boundary Oncomodulin labeling. Measurements for the saccule and cristae used reference-lines drawn along the boundary of the sensory epithelia. For circular histograms, measurements were pooled from three mutants and littermate controls and generated using Oriana circular graphing software (Kovach Computing Services).

Inner ears were dissected from individual mice and coarsely cropped to separate the cochlea and semi-circular canals from the utricle and saccule, and this vestibular portion was transferred to individual Eppendorf tubes and flash frozen in liquid nitrogen. Following PCR genotyping, RNA was extracted from three knockout and three littermate control samples using the QIAGEN RNeasy Micro Kit (QIAGEN 74004) according to the manufacturers protocol. RNA concentration was determined by Nanodrop spectrophotometry and 2.5 µg of RNA was used to prepare cDNA using the Invitrogen SuperScript III Reverse Transcriptase (ThermoFisher Scientific 18080093). Quantitative RT-PCR was performed in a StepOnePlus Real-Time PCR System (Applied Biosystems) and PCR reactions contained 0.6 µM forward and reverse primer, 0.2 μL of cDNA and 2 X Power SYBR Green master mix. Following an incubation at 95 °C for 10 min, the reactions cycled between 95 °C denaturation for 15 s, and 58 °C extension for 1 min 40 times, and a melting curve was generated after the final cycle to verify the amplification specificity. Relative fold changes of gene expression were normalized by against the hair cell gene Pou4f3 since hair cell number would not vary with the size of the cropped vestibule. For each primer set, three biological replicates and two technical replicates were used. PCR amplifications used the following primers: Stk32a primer C (5’- GACTTGACCATGGGAGCCAA –3’), Stk32a primer D (5’-TGGTGTCATTCTTCCGCACA –3’) Stk32a primer E (5’-GGCCCTGGACTACCTACAGA-3’), Stk32a primer F (5’-TAAGGCTTGGTGCCAGCTAC-3’), GAPDH for (5’-TGGAGCCAAAAGGGTCA-3’), GAPDH rev (5’-CTTCTGGGTGGCAGTGA-3’), Pou4f3 for (5’-CCAGACTCCCGAAGATGATGG-3’), Pou4f3 rev (5’-GCCAGCAGGCTCTCATCAAA-3’).

All data is graphed as mean +/- SEM or SD as indicated in figure legends and statistical analysis was conducted using GraphPad Prism 9. The student’s t-test was used to analyze the comparison and a p-value <0.05 was considered to be statistically significant. For measures of GPR156 medial and lateral localization, ne-way ANOVA and unpaired t-test were respectively used to analyze the comparison and p-values <0.05 was considered to be significant. Gpr156 data is graphed as 25–75% boxplots where exterior lines show minimum and maximum values, the middle line the median and +the mean. For analysis of RNAseq datasets, Benjamini-Hirshberg false discover rate was used to normalize data across all transcripts and produce adjusted p-values for significantly downregulated or upregulated genes based on log2-fold changes compared to WT baseline transcript levels. Unless otherwise stated, fluorescent imaging was completed on a minimum of three biological replicates with higher quality representative images selected for publication.

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

This work was supported by the National Institutes of Health (R01DC013066 to MRD, R01DC015242 and R01DC018304 to BT, and Eunice Kennedy Shriver National Institute of Child Health & Human Development of the NIH Award #T32HD007491 to EMR). We thank Doris Wu (NIDCD) for sharing reagents.

All animal work was reviewed for compliance and approved by the Animal Care and Use Committee of The University of Utah (IACUC protocol #00001498) and the Animal Care and Use Committees of The Jackson Laboratory (Animal Use Summary AUS no. 14012).

© 2023, Jia, Ratzan et al.

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