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. Author manuscript; available in PMC: 2017 Oct 26.
Published in final edited form as: Cell Rep. 2017 Oct 17;21(3):666–678. doi: 10.1016/j.celrep.2017.09.079

A Role for Dystonia-Associated Genes in Spinal GABAergic Interneuron Circuitry

Juliet Zhang 1,2,10, Jarret AP Weinrich 1,3,9,10, Jeffrey B Russ 1,2,4, John D Comer 1,2,4, Praveen K Bommareddy 1, Richard J DiCasoli 1, Christopher VE Wright 5, Yuqing Li 6, Peter J van Roessel 7, Julia A Kaltschmidt 1,2,3,8,11,*
PMCID: PMC5658202  NIHMSID: NIHMS913118  PMID: 29045835

SUMMARY

Spinal interneurons are critical modulators of motor circuit function. In the dorsal spinal cord, a set of interneurons called GABApre presynaptically inhibits proprioceptive sensory afferent terminals, thus negatively regulating sensory-motor signaling. Although deficits in presynaptic inhibition have been inferred in human motor diseases, including dystonia, it remains unclear whether GABApre circuit components are altered in these conditions. Here, we use developmental timing to show that GABApre neurons are a late Ptf1a-expressing subclass and localize to the intermediate spinal cord. Using a microarray screen to identify genes expressed in this intermediate population, we find the kelch-like family member Klhl14, implicated in dystonia through its direct binding with torsion-dystonia-related protein Tor1a. Furthermore, in Tor1a mutant mice in which Klhl14 and Tor1a binding is disrupted, formation of GABApre sensory afferent synapses is impaired. Our findings suggest a potential contribution of GABApre neurons to the deficits in presynaptic inhibition observed in dystonia.

In Brief

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GABApre spinal interneurons gate sensory inputs onto motor neurons. Zhang et al. localize GABApre neurons to the intermediate spinal cord and show that these interneurons express hereditary dystonia-related genes Klhl14 and Tor1a. In Tor1a mutant mice, GABApre synapse formation is disrupted, suggesting that spinal circuits may be affected in dystonia.

INTRODUCTION

Spinal interneurons are key components of the neuronal circuits that encode vertebrate motor control. Dysfunction of inhibitory interneurons is thought to contribute to the symptoms of diverse neurologic conditions, including spinal cord injury, amyotrophic lateral sclerosis (ALS), and cerebral palsy (Tillakaratne et al., 2000; Achache et al., 2010; Raynor and Shefner, 1994) and may underlie locomotor defects associated with these conditions such as spasticity and impaired control of voluntary movement (Achache et al., 2010; Comi et al., 2005; Wootz et al., 2013). Yet although injury or disease-related functional deficits have been identified in physiologically defined spinal circuits, little is known about the potential involvement of specific, molecularly defined classes of inhibitory spinal interneurons in the pathophysiology of locomotor disorders.

The monosynaptic stretch reflex, one of the simplest and best-defined spinal circuits, ensures a balance between muscle stretch and contraction, fine-tuning muscle tension to the demands of locomotion. In this circuit, the state of muscle stretch is relayed via proprioceptive sensory neurons to spinal motor neurons, which drive the reflex contraction of the muscle of origin (Eccles et al., 1957; Mears and Frank, 1997). Activity across the sensory-motor synapse is presynaptically modulated by a specific class of GABAergic inhibitory interneurons, called GABApre neurons, that form presynaptic, axo-axonic synapses with sensory afferent terminals (Windhorst, 1996; Rudomin and Schmidt, 1999; Betley et al., 2009; Hughes et al., 2005). GABApre neurons dampen the natural oscillatory movement that would otherwise occur because of the inherent nature of sensory feedback in the spinal reflex circuit, and in their absence, goal-directed movement is severely limited (Fink et al., 2014; Stein and Oğuztöreli, 1976).

Evidence for the involvement of GABApre interneurons in motor diseases comes from physiologic studies in individuals with dystonia, Huntington’s disease, and Parkinson’s disease. People affected by such illnesses display deficits in presynaptic inhibition of spinal sensory-motor activity as measured by the Hoffman reflex (H-reflex) (Knikou, 2008), implicating the involvement of GABApre neurons in their disease pathology (Nakashima et al., 1989; Panizza et al., 1990; Roberts et al., 1994; Priori et al., 1995, 2000; Morita et al., 2000). However, we know little about what role the GABApre-sensory microcircuit may play in disease states and whether changes in this circuitry may reflect causes of, or adaptations to, motor illnesses.

Recent work elucidating the developmental origin, connectivity, and synaptic composition of GABApre neurons demonstrates how H-reflex changes in motor disease may be linked to deficits of presynaptic inhibition. GABApre boutons can be identified by specific molecular markers, including the GABA synthetic enzymes GAD65 and GAD67, and the Ca2+ sensor synaptotagmin-1 (Syt1) (Betley et al., 2009; Hughes et al., 2005). These markers have been used to show that the targeting of GABApre boutons to sensory afferent terminals is mediated in part by an adhesive signaling complex including contactin-5/CASPR4, expressed in sensory neurons, and NrCAM, expressed in GABApre neurons (Ashrafi et al., 2014). Loss of any of these factors results in a decrease in the number of GABApre-sensory afferent synapses (Ashrafi et al., 2014). The molecular composition of GABApre boutons has further been shown to be closely regulated, and alterations in the molecular composition of GABApre boutons lead to alterations in functional presynaptic inhibition (Mende et al., 2016). Changes in presynaptic inhibition witnessed in different motor diseases may therefore be linked to deficits in the assembly, molecular composition, or maintenance of the GABApre microcircuit.

GABApre interneurons can be distinguished by the expression of pancreas transcription factor (Ptf) 1a (Betley et al., 2009; Hughes et al., 2005). However, although Ptf1a marks all dorsal inhibitory interneurons, including GABApre neurons, there is as of yet no specific marker for this functionally distinct GABAergic interneuron subtype. Furthermore, the requirement of Ptf1a for fate specification of dorsal GABAergic interneurons spans the earlyborn dI4 and late-born dILA progenitor populations (Glasgow et al., 2005; Wildner et al., 2006). Although previous work suggests that inhibitory interneurons born during these two major waves of neurogenesis in the dorsal spinal cord give rise to molecularly and functionally distinct interneuron populations (Gross et al., 2002; Müller et al.,2002;Caspary and Anderson, 2003; Helms and Johnson, 2003; Lai et al., 2016), the developmental domain and settling position of GABApre neurons remains relatively unknown.

In this study, we used a conditional genetic strategy for lineage tracing and the timeline of Ptf1a expression to localize the cell bodies of GABApre neurons to the intermediate spinal cord. We further used a comparative microarray analysis to uncover genes specifically enriched by interneurons in the intermediate spinal cord. In an effort to link motor disease pathologies and GABApre circuitry, we focused on genes potentially involved in motor diseases and identified the dystonia-related kelch-like family member protein Klhl14 as a marker of GABApre interneurons. To explore genetic networks related to Klhl14 activity in GABApre interneuronal circuitry, we used a mutant mouse (Dyt1ΔE) in which the binding partner of Klhl14, the more broadly expressed Tor1a, is mutated (Dang et al., 2005).Tor1a encodes a protein in the ATPase family that is involved in protein folding and trafficking (Breakefield et al., 2008; Charlesworth et al., 2013). Humans with dystonia related to analogous mutation in the TOR1A gene further show deficits in presynaptic inhibition (Edwards et al., 2003). Analysis of Dyt1ΔE mice showed a decrease in GABApre bouton number on sensory afferent terminals, suggesting that the Tor1a/Klhl14 pathway plays a role in GABApre-sensory afferent synapse formation. Taken together, our findings help define the organization and genetic profile of a discrete set of intermediate spinal inhibitory interneurons that exert significant modulatory action during motor behavior. More broadly, our results suggest a link between a pathophysiologically relevant genetic lesion and deficits in the synaptic connectivity of a defined spinal neuronal circuit.

RESULTS

Late Ptf1a Expression Distinguishes GABApre Neurons

We first addressed the developmental origins of the GABApre interneuron population. The postmitotic bHLH transcription factor Ptf1a is expressed by dorsal inhibitory interneurons from embryonic day (e) 10.5 until e13.5 (Figures S1A–S1H’) (Glasgow et al., 2005), which corresponds to both early (dI4) and late (dILA) waves of neurogenesis (Gross et al., 2002; Müller et al., 2002). Ptf1aCre mice carrying the tdTomato reporter ROSA26CAG-lsl-tdTomato (Madisen et al., 2010) have previously been shown to label superficial dorsal and intermediately located cell bodies in the developing spinal cord, as well as GABApre boutons on vGluT1-expressing (vGluT1ON) sensory terminals (Figures 1B, 1C, and 1N) (Betley et al., 2009). tdTomato-expressing (tdTomatoON) GABApre boutons on vGluT1ON sensory terminals express both isoforms of the GABA-synthetic enzymes GAD65 and GAD67, known markers of GABApre neurons (Figures 1D and 1E) (Betley et al., 2009; Hughes et al., 2005).

Figure 1. Late Ptf1a Expression Labels GABApre Neurons.

Figure 1

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(A) Ptf1a expression timeline and tamoxifen (TM) injection paradigm.

(B) tdTomatoON cells in the dorsal-intermediate spinal cord of Ptf1aCre; R26tdTomato mice at e18.5.

(C) tdTomatoON (red) boutons on vGluT1ON (blue) sensory afferent terminals in the ventral horn (lamina IX) of p21 Ptf1aCre; R26tdTomato mice.

(D and E) tdTomatoON (red) boutons on vGluT1ON (blue) sensory afferent terminals in lamina IX of Ptf1aCre; R26tdTomato mice co-express GABApre synaptic markers GAD65 (green, D) and GAD67 (green, E).

(F) tdTomatoON cells in the dorsal spinal cord of e9.5 TM-injected Ptf1aCreER; R26tdTomato mice at e18.5.

(G–I) No ventral tdTomatoON projections in e9.5 TM-injected Ptf1aCre; R26tdTomato mice at p21 (G). No tdTomato co-expression with GABApre bouton markers GAD65 (green, H) and GAD67 (green, I).

(J) tdTomatoON cells in the intermediate spinal cord of e12.5 TM-injected Ptf1aCreER; R26tdTomato mice at e18.5.

(K–M) tdTomatoON (red) boutons project into the ventral spinal cord (K) in e12.5 TM-injected Ptf1aCre; R26tdTomato mice at p21 and express GABApre synaptic markers GAD65 (green, L) and GAD67 (green, M).

(N–P) Distribution plots of tdTomatoON neurons in three Ptf1aCre; R26tdTomato (N), six e9.5 TM-injected Ptf1aCreER; R26tdTomato (O), and three e12.5 TM-injected Ptf1aCreER; R26tdTomato mice (P) at e18.5. Numbers represent absolute tdTomatoON neuronal counts.

Scale bars in (B), (F), and (J) represent 100 µm; scale bars in (C), (G), and (K) represent 3 µm; scale bars in (D), (E), (H), (I), (L), and (M) represent 1 mm.

We sought to determine whether GABApre neurons could be assigned to either early or late temporal domains of Ptf1a expression (Figures S1A–S1H’). To accomplish this, we used an inducible Ptf1aCreER mouse line (Pan et al., 2013) crossed to ROSA26CAG-lsl-tdTomato mice and injected tamoxifen (TM) at different time points (Nguyen et al., 2009) (Figure 1A). We found that injecting 100 µg/g TM at e9.5 or e12.5 gives rise to tdToma-toON Ptf1a-derived neurons. Neurons labeled in response to e9.5 TM do not project ventrally (Figures 1G–1I). In contrast, neurons labeled in response e12.5 TM project ventrally, form contacts on vGluT1ON sensory terminals (Figure 1K) and express GAD65 (Figure 1L) and GAD67 (Figure 1M). We thus interpret that TM injections into Ptf1aCreER; R26tdTomato mice at e12.5 label GABApre interneurons and that GABApre neurons must therefore express Ptf1a during the late (dILA) wave of inhibitory interneuron neurogenesis.

To clarify the location of GABApre neurons, we assessed if late-expressing Ptf1a-derived neurons acquire a different cell body position compared with early-expressing Ptf1a-derived neurons. TM injection at e9.5 predominately labels neurons localized to superficial layers of the dorsal horn (Figures 1F and 1O), while TM injection at e12.5 also labels neurons localized to the intermediate spinal cord (Figures 1J and 1P). Taken together, the differences in the spatial distributions of early and late Ptf1a-expressing neurons and synapses suggest that two distinct subdomains of interneurons arise from the Ptf1a-expressing domain, the latter of which comprises the GABApre neuron population in the intermediate spinal cord.

Screen for Motor Disease-Associated Markers Enriched in the Intermediate Spinal Cord

On the basis of these and on previous results suggesting that GABApre neurons reside in the intermediate spinal cord (Betley et al., 2009; Jankowska et al., 1981; Hughes et al., 2005), we sought to compare gene expression profiles of the intermediate spinal cord with more dorsal and more ventral regions in an attempt to uncover potential links between novel GABApre enriched genes and previously identified motor disease associated genes. We and others previously showed that Gad65::N45GFP mice label putative GABApre neurons (Betley et al., 2009; Hughes et al., 2005). Thus the lumbar spinal cords of postnatal day (p) 6 Gad65::N45GFP mice were microdissected into dorsal, intermediate, and ventral regions, where GFP fluorescence was used to delineate the boundaries between the different regions (Figure 2A, inset). Gene expression in each region was quantified by microarray, the results of which were processed to allow a comparative analysis of expression levels between intermediate versus ventral and intermediate versus dorsal regions.

Figure 2. Screen for Novel Genes Expressed in the Intermediate Spinal Cord.

Figure 2

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(A) To find genes enriched in the intermediate spinal cord, gene expression levels were compared between dissected dorsal (D), intermediate (I), and ventral (V) spinal cord regions at p6 (see inset). Genes with significant (p < 0.05) and 2-fold or greater expression changes (268 genes) are graphed as a scatterplot comparing intermediate versus ventral (y axis) and intermediate versus dorsal (x axis) spinal regions. Genes that are upregulated in the intermediate region in both comparisons are in quadrant 1 (Q1, red, 61 genes); genes that are differentially expressed in both comparisons are in quadrants 2, 3, and 4 (Q2, Q3, and Q4, black, 207 genes); and genes that are differentially expressed in either comparison are gray (1,720 genes). Both Gad2 and Klhl14 are upregulated in the intermediate region (Q1).

(B) Functional classification of the 61 genes upregulated in both comparisons identified four main functional families and many other genes of unknown function or classification.

(C) Analyzing in situ hybridization data from the Allen Institute for Brain Science further restricted the 61 candidates to 11 genes (including Klhl14) that showed specific expression in the intermediate spinal cord.

We found 268 genes to be at least 2-fold up-or downregulated on comparison of both intermediate versus ventral and intermediate versus dorsal tissue (Figure 2A, Q1, Q2, Q3, and Q4; p ≤ 0.05, ANOVA). From this list, 61 genes were greater than 2-fold upregulated in the intermediate spinal cord compared with both the dorsal and ventral spinal cord (Figure 2A, Q1; p ≤ 0.05, ANOVA; Table S1). This subset encodes proteins with diverse molecular functions, including DNA binding, ion binding, nucleotide binding, receptors, as well as those with unknown function (Figure 2B). From this list of 61 genes, we evaluated the spinal expression patterns in p4 mice using the Allen Brain Atlas (http://www.brain-map.org). We found 11 candidates to be exclusively expressed in the intermediate spinal cord (Figure 2C, highlighted in Table S1). We assessed these candidates for those that were previously reported to be involved in motor disease. One of these genes was the kelch-like family member protein Klhl14. KLHL14 has been implicated in dystonia because of its direct binding of the torsin family 1, member A (TOR1A) (Giles et al., 2009). A dominant single-amino acid mutation in TOR1A, DYT1ΔE, is highly implicated in early-onset generalized dystonia in humans, leading to sporadic and painful sustained muscle contractions involving both agonist and antagonist muscles (Ozelius et al., 1997; Breakefield et al., 2008).

Klhl14 Is Expressed in Ptf1a-Domain-Derived Interneurons of the Intermediate Spinal Cord

Klhl14 has previously been shown to be expressed in the intermediate e18.5 spinal cord (Wildner et al., 2013). We assessed the expression pattern of Klhl14 during late embryonic and early postnatal stages using in situ hybridization, a time period during which the GABApre-sensory circuit forms (Betley et al., 2009). At late embryonic (e18.5) (Figure 3A) and early postnatal ages (p5 and p10) (Figures 3B and 3C), Klhl14 was expressed in a restricted domain of the intermediate spinal cord, close to the central canal, throughout the rostro-caudal extent of the lumbar spinal cord (Figure 3D, red arrows). We did not detect Klhl14 signal in dorsal root ganglia (DRG), suggesting that Klhl14 is not expressed in sensory neurons (Figure 3D, black arrow).

Figure 3. Klhl14 Expression in Spinal Inhibitory Interneurons.

Figure 3

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(A–E) Klhl14 transcript expression at e18.5 (A), p5 (B and D, red arrows), and p10 (C). There is no Klhl14 expression in DRG (D, black arrow). Dotted line in (D) depicts midline. Klhl14 expression is absent in e18.5 Ptf1a mutant (Ptf1aCre/Cre) spinal cords (E).

(F) Klhl14 transcript co-expression with fluorescently labeled GFPON (green) neurons in the intermediate spinal cord of Ptf1aCre; Thy1YFP mice at p5.

(G) Density plots of combined in situ and immunolabeling showing that at e18.5, Gad2 (blue) expressing Ptf1a-derived cells in e12.5 TM-injected Ptf1aCreER; R26tdTomato mice settle in the intermediate spinal cord (n = 159 cells, three mice). Klhl14 (red) expressing Ptf1a-derived cells in e12.5 TM-injected Ptf1aCreER; R26tdTomato mice settle in the intermediate spinal cord (n = 183 cells, three mice; see also Figures S2A–S2C). Ten to 20 sections per animal were analyzed and plotted in the same graph. Gad2 (blue) and Klhl14 (red) expression patterns in late Ptf1a-derived cells overlap.

Scale bars in (A), (B), and (E) represent 100 µm; scale bars in (C) and (D) represent 100 µm; scale bar in (F) represents 50 µm.

We next asked if Klhl14 was expressed in GABAergic inhibitory interneurons. The transcription factor Ptf1a is required for GABAergic neurotransmitter fate, and in the absence of Ptf1a, the precursors of spinal GABAergic interneurons give rise to excitatory glutamatergic neurons instead (Glasgow et al., 2005). In Ptf1a mutant spinal cords (Ptf1aCre/Cre) (Kawaguchi et al., 2002), we observed no spinal expression of Klhl14 (Figure 3E), as previously reported (Wildner et al., 2013). To further test whether Klhl14 is expressed in Ptf1a-derived GABAergic interneurons, we labeled Ptf1a-derived neurons by intercrossing the Ptf1aCre driver line with mice carrying a Thy1YFP fluorescent protein reporter line (Buffelli et al., 2003) and performed dual immunohistochemistry/in situ hybridization using an anti-GFP antibody and an antisense Klhl14 RNA probe. We found that Klhl14 expression strongly overlapped with YFP-expressing (YFPON) Ptf1a-derived neurons in the intermediate spinal cord (Figure 3F). Given the absence of Klhl14 expression in Ptf1a mutants, we attribute the detection of Klhl14 in neurons that are YFPOFF to the known mosaicism of the Ptf1aCre; Thy1YFP genotype (Betley et al., 2009). Taken together, these results suggest that Klhl14 is expressed in Ptf1a-derived interneurons of the intermediate spinal cord.

To determine whether Klhl4 labels GABApre neurons, we injected TM at e12.5 into Ptf1aCreER; R26tdTomato mice and assessed co-expression of Klhl14 and tdTomato. We found that Klhl14 expression strongly overlapped with tdTomatoON Ptf1a-derived neurons in the intermediate spinal cord (Figures 3G and Figure S2A–S2C). We performed analogous co-expression analysis for tdTomato and Gad2 transcript, the primary molecular marker for GABApre neurons, and similarly saw strong co-localization in the intermediate spinal cord (Figures 3G). The domains of co-expression of Klhl14 and tdTomato, as well as Gad2 and tdTomato, were highly overlapping (Figure 3G), further suggesting that Klhl14 is expressed in GABApre neurons.

No Loss of Ptf1a-Derived Neurons in the Intermediate Spinal Cord of Tor1a Mutants

KLHL14 is a known binding partner of the dystonia 1 protein TOR1A (Giles et al., 2009). Deletion of a single glutamic acid residue in the C-terminal region of TOR1A (ΔE) severely disrupts binding to KLHL14 (Giles et al., 2009), and in humans, this mutation causes early-onset generalized torsion dystonia in an autosomal dominant manner (Ozelius et al., 1997; Breakefield et al., 2008). We therefore assessed whether the Tor1a/Klhl14 pathway could have a functional role in GABApre circuit formation. Analysis of Tor1a expression revealed that it is expressed broadly, including the majority of Ptf1a-derived interneurons in the intermediate spinal cord (Figures 4A and 4B), as well as in proprioceptive sensory neurons in the DRG (Figure 5A). These data confirm that Tor1a and its binding partner Klhl14 are expressed in putative GABApre interneurons in the intermediate spinal cord.

Figure 4. Normal GABApre Neuron Number in Dyt1ΔE Mice.

Figure 4

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(A and B) tdTomatoON (red) neurons in the intermediate spinal cord of Ptf1aCre; R26tdTomato mice. Tor1a (green, B) expression in tdTomatoON (red, A and B) neurons in Ptf1aCre; R26tdTomato mice at p5.

(C and D) tdTomatoON cells in Ptf1aCre; R26tdTomato control (C) and Ptf1aCre; R26tdTomato; Dyt1ΔE (D) mice at p21. Red lines indicate approximate location of GABApre neurons.

(E) The number of putative GABApre neurons is normal in Dyt1ΔE mice compared with controls.

Scale bars in (A) and (B) represent 100 µm; scale bars in (C) and (D) represent 200 µm. Data are reported as mean ± SD.

Figure 5. Abnormal GABApre Circuit Organization in Dyt1ΔE Mice.

Figure 5

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(A) Tor1a (red) is expressed in parvalbumin (Pv)-positive (green) proprioceptive sensory neurons in p6 DRG.

(B) The relative number of proprioceptive sensory neurons per DRG is unchanged between control (white) and Dyt1ΔE mice (black).

(C and D) Increased sensory afferent terminal density (C) and decreased volume (D) are seen in Dyt1ΔE mice compared with controls at p21.

(E) Histogram showing increased numbers of smaller volume sensory afferent terminals in Dyt1ΔE at p21 (control, white; Dyt1ΔE, black; overlap, gray).

(F) Schematic showing sensory neuron (SN) terminals express vGluT1 and are adjacent to Shank1a on motor neurons (MNs). GABApre boutons express GAD65, GAD67, and Syt1.

(G and H) vGluT1ON (blue) sensory afferent terminals are adjacent to Shank1a (red) in WT (G) and Dyt1ΔE mice (H) at p21.

(I and L–M’) Fewer GAD65ON (green)/GAD67ON (red) GABApre boutons (yellow) on vGluT1ON (blue) sensory afferent terminals in p21 Dyt1ΔE mice (M and M′) compared with WT mice (L and L′). Compiled average number of GAD65ON/GAD67ON GABApre boutons on vGluT1ON sensory afferent terminals is reduced by 20.3% in Dyt1ΔE mice (I).

(J and N–O′) Fewer GAD65ON (green)/GAD67ON (red) GABApre boutons (yellow) on vGluT1ON (blue) sensory afferent terminals in 6-month-old Dyt1ΔE animals

(O and O′) compared with WT mice (N and N′). Compiled average number of GAD65ON/GAD67ON GABApre boutons on vGluT1ON sensory afferent terminals is reduced by 27.4% in Dyt1ΔE mice (J).

(K) Histogram showing a shift in the ratio of GABApre boutons per vGluT1 terminal toward fewer GABApre/vGluT1 in Dyt1ΔE mice at p21 (control, white; Dyt1ΔE, black; overlap, gray).

(P and Q) Fluorescence intensity of GAD67 (P) and Syt1 (Q) is unchanged in Dyt1ΔE mice at p21.

Scale bar in (A) represents 50 µm; scale bars in (G) and (H) represent 1 µm; scale bars in (L)–(M′) represent 1 µm. Data are reported as mean ± SD.

One of the major hallmarks of many motor diseases is targeted death of highly specialized cell types (Gorman, 2008; Liang et al., 2014). Given that Klhl14 and Tor1a localize to putative GABApre neurons, we next assessed whether GABApre neuron cell death results from dysfunction in the Tor1a/Klhl14 pathway. As the homozygous Dyt1ΔE mutation is embryonic lethal, we used heterozygous male mice (Dang et al., 2005), which are viable and display motor abnormalities such as defects in beam walking and hyperactivity at 6 months of age (Dang et al., 2005) as well as marked increase in sustained muscle contractions and co-contraction of functionally opposed muscles suggestive of dystonia (DeAndrade et al., 2016). To label putative GABApre neurons, we generated Ptf1aCre; R26tdTomato mice carrying either the Dyt1ΔE or wildtype (WT) allele and quantified the number of fluorescently labeled neurons in the intermediate spinal cord (Figures 4C and 4D). We saw no difference in the number of tdTomatoON, Ptf1a-derived neurons in the intermediate region in Dyt1ΔE compared with control mice (Figure 4E; control: 25.36 ± 3.84 neurons, n = 11 images, three mice; Dyt1ΔE: 24.54 ± 5.17 neurons, n = 13 images, three mice; p = 0.66, two-way ANOVA). We therefore conclude that GABApre neuron number is unchanged in the Dyt1ΔE mutation.

Increased Number of Proprioceptive Terminals in Dyt1ΔE Mice

Because Tor1a is also expressed in proprioceptive neurons of the DRG, we assessed sensory-motor connectivity in Dyt1ΔE mice. We observed no difference in the number of proprioceptive sensory neurons in Dyt1ΔE mice compared with WT (Figures 5A and 5B; control: 142.1 ± 14.1 neurons/DRG, n = 426 neurons, three mice; Dyt1ΔE: 173.4 ± 18.4 neurons/DRG, n = 520 neurons, three mice; p = 0.084, repeated-measures two-way ANOVA). However, the number of vGluT1ON sensory afferent terminals in lamina IX was increased in Dyt1ΔE mice compared with control mice at p21 (Figures 5C and 5E; 1.28-fold; control: 2.81 ± 0.40 terminals/1,000 µm3, n = 2,300 terminals, three mice; Dyt1ΔE: 3.58 ± 0.75 terminals/ 1,000 µm3, n = 2,808 terminals, three mice; p < 0.0001, oneway nested ANOVA). Concomitantly, sensory afferent terminal volume was reduced in Dyt1ΔE mice (Figures 5D and 5E; 0.77-fold; control: 3.92 ± 3.70 µm3, n = 2,300 terminals, three mice; Dyt1ΔE: 3.01 ± 2.82 µm3, n = 2,808 terminals, three mice; p < 0.0001, one-way nested ANOVA). This reduction was driven largely by an increase in the number of sensory afferent terminals with a volume smaller than 5 µm3 (Figure 5E). The alignment of the post-synaptic density marker, Shank1a, with vGlut1ON sensory afferent terminals was unchanged, indicating that sensory-motor synapse formation remains normal (Figures 5F–5H) (Betley et al., 2009). We last assessed for potential changes in sensory activity using GABApre terminal expression of GAD67 as a proxy measure. We previously showed that activity deficits in sensory neurons result in decreased GAD67 synaptic accumulation (Mende et al., 2016). We found no change in GAD67 intensity in GABApre terminals of Dyt1ΔE mice (Figure 5P; control: 1.00 ± 0.60 normalized GAD67 fluorescence intensity, n = 271 synapses, three mice; Dyt1ΔE: 0.94 ± 0.55 GAD67 fluorescence intensity, n = 212 synapses, three mice; p = 0.215, nested ANOVA). The unchanged level of GAD67 suggests that sensory activity is unperturbed in Dyt1ΔE mice.

GABApre Bouton Number Is Decreased in Tor1a Mutant Mice

We next assessed whether GABApre synaptic organization was affected in Dyt1ΔE mice. We used the co-expression of GAD65 and GAD67 (GAD65ON/GAD67ON) abutting vGluT1ON sensory terminals to label GABApre-sensory afferent synapses (Figure 5F) (Betley et al., 2009). We quantified the number of GAD65ON/GAD67ON boutons at p21 when locomotor circuits have finished developing (Figures 5L–5M′), as well as at 6 months (Figures 5N–5O′) when a behavioral motor defect is first observed in Dyt1ΔE mice (Dang et al., 2005). We found 20.3% and 27.4% reductions in the number of GAD65ON/GAD67ON boutons on vGluT1ON sensory terminals in Dyt1ΔE mice compared with WT controls at p21 (Figures 5I, 5K, and 5L–5M′; WT: 2.35 ± 2.12, n = 287 boutons, three mice; Dyt1ΔE: 1.87 ± 1.67, n = 287 boutons, three mice; p < 0.01, one-way nested ANOVA) and 6 months, respectively (Figures 5J and 5N–5O′ ; WT: 2.51 ± 2.22, n = 287 boutons, three mice; Dyt1ΔE: 1.82 ± 1.78, n = 287 boutons, three mice; p < 0.0001, one-way nested ANOVA). We did not find any changes in the number of GAD65- or GAD67-only-expressing terminals apposing vGluT1ON sensory afferent terminals (data not shown). These findings suggest that the Tor1a/Klhl14 pathway is required for organizing the proper number of GABApre boutons per sensory terminal.

Dyt1ΔE mice have been shown to have deficits in synaptic vesicle recycling and synaptic protein stabilization in neural tissues such as the hippocampus and cerebellum (Granata et al., 2011; Kim et al., 2010). However, we do not see changes in the fluorescence intensity of synaptic vesicle marker Syt1 in Dyt1ΔE mice compared with controls at p21, as measured by immunofluorescence confocal imaging (Figure 5Q; relative fluorescence intensity change: control: 1.00 ± 0.64, n = 369 boutons, three mice; Dyt1ΔE: 1.16 ± 0.74, n = 578 boutons, three mice; p = 0.14, one-way nested ANOVA). This finding, together with the stability of GABApre terminal GAD67 intensity described above (Figure 5P), suggests that GABApre synaptic differentiation remains unaltered.

DISCUSSION

Spinal interneurons are essential for modulating locomotor behavior, but their potential involvement in many motor diseases is unclear. Deficits in presynaptic inhibition of proprioceptive sensory afferents have been observed in human patients with movement disorders or focal motor deficits (Nakashima et al., 1989; Panizza et al., 1990; Priori et al., 2000; Berardelli et al., 1998), suggesting a potential role for spinal GABApre interneurons in the pathophysiology of such disorders. In this study, we found that late Ptf1a-expressing neurons give rise to the GABApre interneuron subpopulation. Guided by their localization, we performed a microarray screen and identified that the kelch-like family member protein Klhl14 is expressed in GABApre interneurons. Our findings reveal that mutation of the Klhl14 binding partner Tor1a, a hereditary dystonia-related gene, at a site that disrupts binding to Klhl14, leads to measurable deficits in GABApre-sensory neuron connectivity. Our data thereby suggest a role for dystonia-related genes in the development of spinal sensory-motor circuitry.

Position and Developmental Origin of GABApre Interneurons

In this work, we provide evidence that the cell bodies of ventrally projecting GABApre interneurons are located in the intermediate spinal cord and demonstrate that their segregation to this region correlates with the developmental timing of transcription factor expression. Interneuronal diversification in the spinal cord begins embryonically with discrete progenitor domains giving rise to specific precursor populations. A first wave of neurogenesis (e10–e11.5) gives rise to dorsal inhibitory interneurons of the dI4 domain, and a second wave of neurogenesis (e12–e14.5) generates dorsal inhibitory interneurons of the dILA domain (Gross et al., 2002; Müller et al., 2002). Previous positional studies suggest that the majority of dI4 interneurons remain in the deep dorsal horn, while dILA interneurons migrate to the superficial dorsal horn (Müller et al., 2002; Gross et al., 2002; Helms and Johnson, 2003; Caspary and Anderson, 2003). Our molecular labeling and developmental timing studies now identify GABApre interneurons as localized to the intermediate spinal cord and emerging from dILA during the second wave of neurogenesis. This appears to contradict the prevalent model that the later-born dILA interneurons populate the superficial dorsal horn, but it is consistent with the findings of Nornes and Carry (1978), whose autoradiographic studies show that later-born interneurons (e12–e13) populate both superficial dorsal and medial regions of the dorsal lumbar spinal cord and that only medially located cells are marked by labeling at e14.

Timed Transcription Factor Expression in Neuronal Circuitry

Ptf1a is required for the development of inhibitory neurons throughout the CNS (Jusuf and Harris, 2009; Pascual et al., 2007). Previous molecular-anatomical work inferred at least two different populations of Ptf1a-expressing synapses (Betley et al., 2009): (1) a peptidergic and glycinergic one that forms axo-axonic contacts on cutaneous sensory afferent terminals in the dorsal spinal cord and (2) the GABApre terminals that are neither glycinergic nor peptidergic but express GAD65, GAD67, and Syt1 and form direct axo-axonic connections with proprioceptive sensory afferent terminals in the intermediate and ventral spinal cord (Betley et al., 2009; Hughes et al., 2005). Electrophysiological evidence further suggests that these distinct populations of synapses arise from spatially segregated cell populations with different functions. A dorsal interneuron population is thought to be involved in presynaptic inhibition of cutaneous sensory afferent terminals in the dorsal spinal cord, while an intermediate population participates in presynaptic inhibition of proprioceptive sensory afferent terminals in the intermediate and ventral spinal cord (Jankowska et al., 1981). An intermediate location of GABApre neurons is also suggested by co-expression of the GABApre hallmark genes Gad65 and Gad67 in neuronal cell bodies of the intermediate spinal cord (Betley et al., 2009), and labeling of GAD65-GFP-expressing cell bodies in the intermediate spinal cord following injection of a tracer dye into the ventral motor column to which GABApre neurons project (Hughes et al., 2005). We now identify GABApre interneurons as an intermediate population distinct from other Ptf1a-expressing dorsal GABAergic interneurons.

Our results suggest a relationship between the timing of transcription factor expression and neuronal settling position, circuit connectivity, and function. As such, our work supports and extends previous findings showing that multiple aspects of neuronal fate, including migratory behavior and ultimate cell body positioning, are associated with timing of neurogenesis (Tripodi et al., 2011; Benito-Gonzalez and Alvarez, 2012; Stam et al., 2012; Tripodi and Arber, 2012). Several recent findings further suggest that cell body position correlates with sensory input connectivity of both motor neurons (Sürmeli et al., 2011) and interneurons (Tripodi et al., 2011; Bikoff et al., 2016). The dorsal-medial location of GABApre cell bodies positions them in a region of spinal cord densely innervated by descending corticospinal tract axons (Bareyre et al., 2005; Russ et al., 2013) and supports a role for GABApre interneurons in integrating descending cortical inputs into the regulation of the sensory-motor reflex circuit (Azim et al., 2014). The late expression of Ptf1a could thereby play a dual role in (1) guiding GABApre neurons to a settling position within the spinal cord that ensures proper input from supraspinal, spinal, and sensory neurons and (2) initiating signaling cascades that determine their efferent proprioceptive targeting.

Tor1a Function in GABApre Circuitry

Our study further supports a role for Tor1a in GABAergic synaptogenesis, given the decrease in GABApre-sensory afferent synapses we observe in Dyt1ΔE mice. Tor1a is a broadly expressed AAA+-class ATPase, intracellularly localized to the nuclear envelope and endoplasmic reticulum, postulated to function as a chaperone protein and in the modification and processing of protein complexes through secretory pathways. Tor1a is enriched in developing neuronal tissues and has been identified in the cytosol and neurites of neurons, including both the axonal and dendritic compartments of GABAergic Purkinje cells in the cerebellum (Puglisi et al., 2013; Breakefield et al., 2008). Functionally, Tor1a has been shown to play a role in synaptic vesicle recycling (Granata et al., 2008, 2011) and in synaptic vesicle release (Yokoi et al., 2013). Structurally, in mouse cerebellum, there is a decrease in inhibitory synaptic contacts on Purkinje cells in both Tor1a+/− mice and mice carrying the human Dyt1ΔE mutation, suggesting that GABAergic synaptogenesis is compromised in the presence of mutant Tor1a (Vanni et al., 2015).

How dysfunction of Tor1a contributes to the decreased number of GABApre-sensory afferent synapses remains an outstanding question. The DYTΔE mutation disrupts binding of TOR1A to KLHL14 (Giles et al., 2009). Little is known about Klhl14, yet another member of the Kelch-like protein family, Klhl1, modulates voltage-gated calcium channels (Nemes et al., 2000) and regulates neurite and cellular process extension (Seng et al., 2006; Jiang et al., 2007). Knockdown of Klhl1 in rat hippocampal cultures results in decreased numbers of excitatory and inhibitory synapses (Perissinotti et al., 2015). The loss of synapses seen in Dyt1ΔE mice hints that Klhl14 may have a similar role to Klhl1. If Klhl14 binds actin like Klhl1 (Nemes et al., 2000), this would support models of Tor1a’s function at the interface of synaptic membrane recycling and local cytoskeletal dynamics (Granata et al., 2009). Given that the Dyt1ΔE phenotype of decreased GABApre-sensory afferent synapse number is strikingly similar to that seen following deletion of Ig-superfamily adhesion molecules expressed in GABApre interneurons or their sensory afferent partners (Ashrafi et al., 2014), it is further tempting to speculate that adhesive signaling may be affected by Dyt1ΔE. Tor1a has been shown to interact with components of the dystrophin-associated glycoprotein complex (DGC) (Esapa et al., 2007). Dystroglycan, a component of the DGC, binds to neurexin (Sumita et al., 2007) and indirectly interacts with NL2 (Sugita et al., 2001), an adhesion molecule also found to localize to sensory neurons (Ashrafi et al., 2014). This suggests a potential role for Tor1a in adhesion molecule localization in the GABApre-sensory neuron connectivity (Puglisi et al., 2013; Patrizi et al., 2008).

Our data cannot formally distinguish whether Tor1a functions in GABApre interneurons or in sensory neurons to influence GABApre-sensory afferent synapse number. Tor1a is expressed in both GABApre interneurons and proprioceptive sensory neurons, while its reported binding partner Klhl14 is not expressed in sensory neurons. This may point to different functions for Tor1a in these distinct neuronal populations. The fact that the Dyt1ΔE mutation abolishes binding of Klhl14 to Tor1a suggests that the GABApre phenotype we observe reflects Klhl14’s function in GABApre interneurons. Tor1a likely functions in oligomers, however, and its ability to bind itself may also be compromised by the Dyt1ΔE mutation (Pham et al., 2006). We do see an increase in the number of smaller volume sensory afferent terminals in Dyt1ΔE mice, leading to the possibility that the decrease in the number of GABApre boutons per sensory afferent terminal is due to an increased number of smaller sensory afferent terminals, which are known to have fewer GABApre boutons (Pierce and Mendell, 1993; Betley et al., 2009). However, estimating the loss of GABApre boutons due to the size principle using previously published data (Pierce and Mendell, 1993) would account for an approximately 7% decrease in GABApre synapses per sensory afferent terminal and therefore would not explain the markedly greater GABApre bouton loss seen in Dyt1ΔE mice (see Supplemental Experimental Procedures). This analysis, together with our finding that intensity of GABApre terminal GAD67 is unchanged—suggesting against alterations in sensory afferent activity state— leads us to see as unlikely the possibility that GABApre terminal number is decreased due to a non-autonomous effect of Tor1a in sensory neurons.

Tor1a is known to be expressed throughout the CNS, including the cerebral cortex, basal ganglia, midbrain, and cerebellum (Granata et al., 2009). As such, a further possibility is that Tor1a mutation generates a non-cell-autonomous synaptic phenotype via function outside the GABApre-sensory microcircuit, for example in CNS regions that send descending projections into the spinal cord. GABApre interneurons receive direct synaptic input from corticospinal tract (CST) axons (Russ et al., 2013), and disruption of CST-GABApre connectivity via cortical lesion results in no change in the number of GABApre-sensory afferent synapses. This is notably in contrast to the Dyt1ΔE mutant phenotype we describe here, in which synaptic number is altered. This contrast leads us to interpret that the Tor1a phenotype does not arise from disruption of descending CST tracts.

The pathophysiology of early-onset primary dystonia has focused on the basal ganglia, particularly the role of cholinergic interneurons in the striatum (Perlmutter and Mink, 2004; Goodchild et al., 2013; Pappas et al., 2015). However, dystonias, including the DYT1-associated early-onset dystonias, are known to be associated with deficits in spinal reciprocal inhibition of the H-reflex, particularly the late phase of this inhibition, believed to be mediated by presynaptic inhibition of sensory afferents (Berardelli et al., 1998; Nakashima et al., 1989; Panizza et al., 1990; Priori et al., 2000). These deficits in presynaptic inhibition have been proposed to reflect alterations in descending corticospinal control of spinal interneurons (Nakashima et al., 1989). Our work, however, identifies the subpopulation of spinal interneurons responsible for presynaptic inhibition and shows that in the presence of dysfunctional Tor1a protein, these interneurons make fewer presynaptic inhibitory contacts on primary sensory afferent neurons. Although the decrement in GABApre terminal number is limited, we know from our previous work that a comparably modest decrease in GABApre terminal GAD67 expression can have a robust impact on measured presynaptic inhibition (Mende et al., 2016). As such, we suggest that deficits in spinal circuits may work in concert with concurrent well-known changes in the basal ganglia, cerebellum, and other supraspinal regions of the CNS to drive motor coordination deficits in dystonia. We propose that focus on the specific interneuron subclasses that constitute the spinal circuitry of movement may better enhance our understanding of the causal factors underlying the complex functional manifestations of motor disease.

EXPERIMENTAL PROCEDURES

Mouse Strains

The following mouse strains were used in this study: Dyt1ΔE (Dang et al., 2005), Gad65::N45GFP (López-Bendito et al., 2004), Ptf1aCre (Kawaguchi et al., 2002), Ptf1aCreER (Pan et al., 2013), R26CAG–lox–STOP–tdTomato/+ (Jackson Labs, Ai14) (Madisen et al., 2010), and Thy1lox-STOP-YFP (line 15) (Buffelli et al., 2003). Dyt1ΔE mice were analyzed as heterozygotes, as homozygous animals die (Dang et al., 2005). Experiments conform to the regulatory standards of the Institutional Animal Care and Use Committee of Memorial Sloan Kettering Cancer Center.

TM Injections

TM (T-5648; Sigma-Aldrich) was dissolved in corn oil (C-8267; Sigma-Aldrich) at a final concentration of 20 mg/mL. TM was intraperitoneally injected once into pregnant dams at 9.5 or 12.5 days post-coitus, and pups were harvested at e18.5 or p21. For embryo harvest, 80–100 mg/kg TM was administered at both time points. For postnatal harvest, 20 mg/kg TM was administered at e9.5, and 100 mg/kg TM was administered at e12.5.

Histochemistry

Immunohistochemistry and in situ hybridization on 12-or 20-µm-thick cryostat sections were performed as previously described (Arber et al., 1999; Betley et al., 2009) with the following modification: mice were perfused by peristaltic pump (World Precision Instruments) with a 2% heparin (Butler-Schein) normal saline solution flush, followed by room temperature 4% paraformaldehyde (PFA).

Antibodies were used in 0.3% Triton-X in PBS with 1% BSA or 0.1% PBT with 1% BSA. The following antibodies were used in this study: rabbit anti-GAD65 (1:8,000) (Betley et al., 2009), mouse anti-GAD67 (1:10,000; Millipore), rabbit anti-GFP (1:1,000; Invitrogen), guinea pig anti-Lmx1b (1:8,000; generously provided by S. Morton and T. Jessell) (Kania et al., 2000), chicken anti-parvalbumin (1:1,000; generously provided by S. Morton and T. Jessell) (de Nooij et al., 2013), rabbit anti-Ptf1a (1:5,000; generously provided by C. Wright), guinea pig anti-RFP (1:2,000; generously provided by N. Betley) (Betley et al., 2013), rabbit anti-RFP (1:1,000; Rockland), rabbit anti-Runx3 (1:4,000; generously provided by S. Morton and T. Jessell) (Chen et al., 2006), rabbit anti-Shank1a (1:1,000; Millipore), rabbit anti-Tor1a (1:600; Millipore), guinea pig anti-vGluT1 (1:32,000) (Betley et al., 2009), and fluorophore-conjugated secondary antibodies (Jackson Labs and Molecular Probes).

In situ hybridization combined with antibody staining was performed as described (Ashrafi et al., 2014). tdTomato or GFP detection in combination with in situ hybridization was performed with additional tyramide signal amplification (TSA) (Perkin-Elmer) of the RFP or GFP antibodies with donkey anti-rabbit HRP-conjugated secondary (1:1,000; Millipore). In situ hybridization of Gad2 (Russ et al., 2015) and Klhl14 (generously provided by H. Wildner and C. Birchmeier) (Wildner et al., 2013) was performed with DIG-labeled riboprobes.

Synaptic Quantification

GABApre/vGluT1 synaptic number counts were performed using Leica LASAF software plug-in (version 2.6.0.7266) on z stacks (0.3 µm optical sections) obtained on a Leica TCS SP5 confocal. At least three mice per genotype were analyzed and 99 vGluT1ON sensory afferent terminals were counted per animal. Sensory afferent terminal number, volume, and GABApre fluorescence intensity were analyzed in the 3D image analysis program Imaris. Statistics on Imaris data were performed in MATLAB. Differences between WT/control and mutant mice were determined one-way nested ANOVA unless otherwise indicated, with p > 0.05 not significant, **p < 0.01, and ****p < 0.0001. We used box-and-whisker plots where individual data points are either images or synapses within images and scatterplots where data points are individual animals. Data are reported as mean ± SD.

Candidate Screen

Spinal cords were removed from three p6 Gad65::N45GFP mice, embedded in UltraPure L.M.P. agarose (Invitrogen), and vibratome-sectioned at 300 µm. The dorsal, intermediate, and ventral regions were then dissected from each section and flash-frozen on dry ice. RNA was obtained by Trizol extraction and run on an Affymetrix Mouse Genome 430 2.0 Array. Gene expression data were analyzed using the BioConductor suite of tools (http://www.bioconductor.org) in R statistical language (http://www.r-project.org). The data were normalized using standard gcrma function. For each group comparison, differentially expressed genes were sought using limma package with a p value cutoff of 0.05 (adjusted for multiple hypothesis testing) and fold changes of 2. Pathway analysis was done using the functional annotation tool DAVID (https://david.ncifcrf.gov).

Positional Analysis

Probability densities of tdTomato-positive (tdTomatoON) cell body position were calculated in e18.5 Ptf1aCre; R26tdTomato embryos following TM injection at e9.5 and e12.5. Positional coordinates of tdTomatoON cell bodies were obtained using software developed in the laboratory (Russ et al., 2013). The positional coordinates were then processed in R statistical language using the kde2d function from the MASS package. Further computation and graphical display were performed in R using the hexabin package (https://cran.r-project.org/web/packages/hexbin/index.html).

Proprioceptive Sensory Neuron Quantification

Confocal images of DRG sections were evaluated by eye by two separate counters, with the counter blind to genotype. Cells expressing both parvalbumin and Runx3 were counted as proprioceptors. Statistics were generated using repeated-measures two-way ANOVA to compare any effects due to genotype and counter using Prism statistical software.

Supplementary Material

1

Highlights.

  • Developmental lineage analysis localizes GABApre neurons to intermediate spinal cord

  • Microarray screen identifies genes expressed in the GABApre population

  • Dystonia-related genes Klhl14 and Tor1a are expressed in the GABApre population

  • Dystonia-causing Tor1a mutation Dyt1ΔE alters GABApre-sensory connectivity

Acknowledgments

We are grateful to Drs. Nicholas Betley, Subhamoy Das, Jane Johnson, Joseph Pierce, and Roy Sillitoe for comments on the manuscript. We thank Nicholas Betley, Susan Morton, and Thomas Jessell for antibodies, Hendrik Wildner and Carmen Birchmeier for the Klhl14 clone, Teresa Milner for advice and guidance with pump perfusions, Alexandra Joyner for the TM protocol and advice, Josephine Belluardo for perfusion assistance and advice, Aanchal Tyagi for cell counts, and Raya Khanin and the Sloan Kettering Genomics and Bioinformatics cores for screen analysis and statistics. This work was supported by the Graduate Student Research Program (GSRP) through the National Aeronautics and Space Administration under award number NNX10AL58H (J.A.P.W.), a Medical Scientist Training Program (MSTP) grant from the National Institute of General Medical Sciences of the NIH under award number T32 GM007739 to the Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program (J.B.R., J.D.C.), NIH grants DK42502 and DK089570 (C.V.E.W.), and the Vanderbilt Center for Imaging Shared Resource, partly supported through the Vanderbilt University Medical Center Digestive Disease Research Center, Diabetes Research Training Center, and Vanderbilt Ingram Cancer Center, supported by NIH grants CA68485, DK20593, and DK58404, Memorial Sloan Kettering (MSK) Cancer Center Support Grant/Core Grant P30 CA008748, and NIH grant R01 NS083998 (J.A.K.).

Footnotes

DATA AND SOFTWARE AVAILABILITY

The accession number for the data reported in this paper is GEO: GSE99590.

SUPPLEMENTAL INFORMATION

Supplemental Information includes Supplemental Experimental Procedures, two figures, and one table and can be found with this article online at https://doi.org/10.1016/j.celrep.2017.09.079.

AUTHOR CONTRIBUTIONS

J.Z. performed Ptf1a timing study, Klhl14 expression analysis, and Dyt1ΔE mutant analysis. J.A.P.W. performed the screen for intermediate enriched genes, and Dyt1ΔE mutant and data analysis. J.B.R. conceived of the idea of temporally distinguishing interneuron subpopulations and established the paradigm for TM injections. J.D.C. helped with preparing tissue for the screen and provided cell distribution data analysis. P.K.B. and R.J.D. provided technical assistance. C.V.E.W. provided reagents. Y.L. generated Dyt1ΔE mice. J.Z., J.A.P.W., and J.A.K. designed the study. J.Z., J.A.P.W., P.J.v.R., and J.A.K. interpreted results and wrote the manuscript.

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