The X-Linked Autism Protein KIAA2022/KIDLIA Regulates Neurite Outgrowth via N-Cadherin and δ-Catenin Signaling

Abstract Our previous work showed that loss of the KIAA2022 gene protein results in intellectual disability with language impairment and autistic behavior (KIDLIA, also referred to as XPN). However, the cellular and molecular alterations resulting from a loss of function of KIDLIA and its role in autism with severe intellectual disability remain unknown. Here, we show that KIDLIA plays a key role in neuron migration and morphogenesis. We found that KIDLIA is distributed exclusively in the nucleus. In the developing rat brain, it is expressed only in the cortical plate and subplate region but not in the intermediate or ventricular zone. Using in utero electroporation, we found that short hairpin RNA (shRNA)-mediated knockdown of KIDLIA leads to altered neuron migration and a reduction in dendritic growth and disorganized apical dendrite projections in layer II/III mouse cortical neurons. Consistent with this, in cultured rat neurons, a loss of KIDLIA expression also leads to suppression of dendritic growth and branching. At the molecular level, we found that KIDLIA suppression leads to an increase in cell-surface N-cadherin and an elevated association of N-cadherin with δ-catenin, resulting in depletion of free δ-catenin in the cytosolic compartment. The reduced availability of cytosolic δ-catenin leads to elevated RhoA activity and reduced actin dynamics at the dendritic growth cone. Furthermore, in neurons with KIDLIA knockdown, overexpression of δ-catenin or inhibition of RhoA rescues actin dynamics, dendritic growth, and branching. These findings provide the first evidence on the role of the novel protein KIDLIA in neurodevelopment and autism with severe intellectual disability.


Introduction
Autism spectrum disorder (ASD) is described on the basis of its three core symptoms: diminished language and communication, impaired social interactions, and the tendency for repetitive behaviors (Lord et al., 1989). ASD is becoming increasingly devastating due to its high prev-alence, impact on families, and cost to society. Approximately one in 68 individuals in the United States has ASD, and roughly 30% of those with ASD have intellectual disability (ID;Baio, 2014).
The mammalian X chromosome is enriched with genes expressed in the brain, as demonstrated by the high incidence of X-linked ID (Skuse, 2005;Nguyen and Disteche, 2006). Previous work from our group and others identified loss of function of KIDLIA (also referred to as KIAA2022 or Xpn) at chromosome Xq13.2 as the gene responsible for severe ID and autistic behavior in several families (Cantagrel et al., 2004(Cantagrel et al., , 2009Ishikawa et al., 2012;Van Maldergem et al., 2013;Charzewska et al., 2014;Kuroda et al., 2015). We have previously shown that knockdown of KIDLIA in rat hippocampal neurons led to impaired neurite outgrowth (Van Maldergem et al., 2013). Patients with a loss of KIDLIA show symptoms typical of ASD including febrile seizures, repetitive behaviors, impaired language, microcephaly, and strabismus (Cantagrel et al., 2004(Cantagrel et al., , 2009Van Maldergem et al., 2013), establishing the gene as a causal factor for ASD with ID.
Accumulating evidence has shown that alterations in neurite outgrowth and branching are a common phenotype in neurodevelopmental disorders including ID and ASD (DiCicco-Bloom et al., 2006;Zikopoulos and Barbas, 2010). Many autism-related mutations, such as those in phosphatase and tensin homolog on chromosome 10, tuberous sclerosis complex 1, or SHANK3, result in an excess of branching (Kwon et al., 2006;Peça et al., 2011;Weston et al., 2014). Others, such as mutations in methyl CpG binding protein 2, thousand and one kinase 2, and endosomal Na ϩ /H ϩ exchanger 6, lead to diminished branching (Belichenko et al., 2009;de Anda et al., 2012;Ouyang et al., 2013). As KIDLIA is a novel gene product involved in autism with severe ID, its role in brain development including neurogenesis, neuron migration, and neuron morphogenesis has not been investigated. Our previous work has suggested an involvement of KIDLIA in neurite outgrowth (Van Maldergem et al., 2013), but the molecular mechanisms remain unknown.
N-cadherin-mediated extracellular interactions have been shown to be required for dendrite growth (Tan et al., 2010). A major molecule that interacts with the cytoplasmic C terminus of N-cadherin is ␦-catenin. ␦-Catenin, a member of the p120 catenin family, is neuron specific and binds to the juxtamembrane segment of N-cadherin (Lu et al., 1999). ␦-Catenin is a major candidate gene in autism and part of a protein network that is strongly involved in regulating dendrite growth (Turner et al., 2015). Overexpression of ␦-catenin can induce dendritic protrusions in hippocampal neurons (Martinez et al., 2003), whereas loss of ␦-catenin reduces dendritic growth and branching (Elia et al., 2006;Arikkath et al., 2008).
For the first time, we report a role for KIDLIA in neuron migration and dendrite morphological development. We show that KIDLIA is expressed exclusively in the nucleus and is neuron specific. We find that loss of KIDLIA produces aberrant neuronal migration with major defects in apical dendrite growth and orientation in vivo. Knockdown of KIDLIA in vitro results in a decrease in dendritic growth and actin dynamics. A loss of KIDLIA also leads to increased N-cadherin at the plasma membrane and an elevated interaction between N-cadherin and ␦-catenin. This increased association depletes the cytoplasmic pool of ␦-catenin, causing activation of RhoA-GTP. Consistent with this, we find that after KIDLIA knockdown in neurons, overexpressing ␦-catenin or inhibiting RhoA activity rescues the defects in dendritic growth and actin dynamics. These findings strongly support a role for the N-cadherin/ ␦-catenin-RhoA signaling system in the KIDLIA-dependent dysregulation of dendritic morphogenesis, providing novel insights into the mechanism of KIDLIA-dependent autism and ID.

Neuronal transfection and viral infection
Hippocampal neurons were transfected at the time of plating in six-well glass-bottom dishes for FRAP experiments using Lipofectamine 2000 (Thermo Fisher Scien-tific, Waltham, MA; cat. # 11668019) and the target plasmid DNA or siRNA per the manufacturer's suggestion. For live imaging experiments, neurons were transfected at DIV5. For one well containing 2 ml plating medium ϩ cells, 3 l Lipofectamine 2000 and 1 g plasmid DNA ϩ 2 l siRNA (20 M) were first separately diluted in 50 l minimal essential medium then mixed and incubated at room temperature for 20 min to form the transfection complex. The transfection complex was added to the wells and incubated at 37°C for 4 h before the medium was removed and replaced with feeding medium. Neurons were then cultured for stated times for FRAP or live imaging experiments.
Recombinant lentiviruses were produced by transfecting HEK293T cells with plasmids for the shRNA constructs with viral packaging and envelope proteins (pRSV/ REV, pMDLg/RRE, and pVSVG) using polyethylenimine reagent (Polysciences, Warrington, PA; cat. # 23966). Conditioned medium containing lentivirus was harvested after 48 h, centrifuged at 1000 ϫ g for 10 min, filtered through a 0.45-m filter, and stored at Ϫ80°C. Neurons were infected with lentivirus on the day of plating, and medium was changed 1 d later to feeding medium.

Animals
Timed pregnant CD-1 mice were purchased from Charles River Laboratories (Cambridge, MA; strain code 022) for in utero electroporation experiments. All animals were maintained in accordance with guidelines of the Boston University Institutional Animal Care and Use Committee. Care was taken to minimize suffering of the animals during surgical procedures. The first neonatal day was considered to be postnatal day 0 (P0).

In utero electroporation
In utero electroporation (IUE) was performed as described previously (Gal et al., 2006) on timed pregnant CD-1 dams at embryonic day 14.5. Briefly, dams were anesthetized via i.p. injection of a ketamine/xylazine mixture, and the uterine horns were exposed via midline laparotomy. One to two microliters of plasmid DNA mixed with 0.1% fast green dye (Sigma-Aldrich; cat. # F7258) was injected intracerebrally through the uterine wall and amniotic sac using a pulled-glass micropipette. The plasmid vectors were used at a final concentration of 2-3 g/l. The anode of a Tweezertrode (Harvard Apparatus, Holliston, MA) was placed over the dorsal telencephalon above the uterine muscle, and four 35-V pulses (50-ms duration separated by a 950-ms interval) were applied with a BTX ECM830 pulse generator (Harvard Apparatus). After electroporation, the uterine horns were returned to the abdomen, the cavity was filled with a warm saline solution, and the incisions were closed with silk sutures. The dams were then placed in a clean cage and monitored closely during recovery. The pups were allowed to mature with the mother until the times indicated. To collect the electroporated brains, animals were anesthetized with an i.p. injection of ketamine/xylazine and transcardially perfused with ice-cold PBS. The brains were removed and placed into 4% paraformaldehyde in PBS solution at 4°C for 6 h, followed by overnight incubation in a 30% sucrose PBS solution at 4°C. The brains were placed in trays and submerged in optimum cutting temperature embedding medium (Tissue-Tek; cat. # 25608-930) and flash frozen by placing the trays in a bath of methanol mixed with dry ice. Frozen brains were cut in 35-m sections on a Leica CM 1850 cryostat (Leica Biosystems, Buffalo Grove, IL) at -20°C. These procedures were reviewed and approved by the Boston University Institutional Animal Care and Use Committee.

Immunocytochemistry
Hippocampal neurons were washed twice in ice-cold artificial cerebrospinal fluid (ACSF) and fixed for 10 min in a 4% paraformaldehyde/4% sucrose solution at room temperature. Cell membranes were permeabilized for 10 min in 0.3% Triton X-100 (Sigma-Aldrich; cat. # T-9284) in PBS, rinsed three times in PBS, then subjected to a blocking procedure (1 h PBS ϩ 5% goat serum). After blocking, cells were incubated with primary antibodies (in 5% goat serum and PBS) for 2 h at room temperature, washed, and incubated with Alexa Fluor-conjugated fluorescent secondary antibodies (1:700) for an additional hour. Cells were then mounted to microscopy glass slides with Prolong Gold anti-fade mounting reagent (Thermo Fisher Scientific; cat. # P36930) for visualization.

Microscopy
For in vitro analysis of neuronal morphology, a Zeiss inverted fluorescent microscope was used to collect images with a 40ϫ oil-immersion objective [numerical aperture (NA) 1.3] and collected with AxioVision Release 4.5 software. Neuron images were quantified in Sholl analysis using NIH ImageJ (see below).
Brain sections taken after IUE were imaged using a Zeiss LSM 700 laser scanning confocal microscope. Z-stack images (25 m, 40ϫ) were acquired using the Zen software package. GFP-positive cells were traced with the NeuronJ plugin in ImageJ for analysis of dendrite morphology. Sections from at least three embryos were counted and analyzed for each experiment, and surgeries for each combination of plasmids were repeated to confirm the results.

Sholl analysis
MAP2-positive dendrites were traced from images of neurons stained with MAP2 and tau1 using the NeuronJ (RRID: SCR_002074) plugin in ImageJ (RRID: SCR_ 003070). The Snapshot tool in NeuronJ was used to save the tracings as an image file that was converted to 8-bit, and these images were analyzed with the Sholl analysis plugin in ImageJ. The range of measurement was set using the straight line tool traced from the center of the soma to the outermost neurite. Dendrite intersections were analyzed from a starting radius of 10 m with 10-m steps to the outer radius. The resulting numbers of intersections per cell were used to calculate the mean and SEM for each radius interval. Treatments were applied to sister cultures that originated from the same neuron culture preparation.

Western blot
Cortical neurons cultured in either 60 mm dishes (3 ϫ 10 6 cells/dish) or six-well plates (10 6 cells/well) were treated with virus at the time of plating and any other drugs as stated. Neurons were lysed in Laemmli 2ϫ sample buffer (4% SDS, 10% 2-mercaptoethanol, 20% glycerol, 0.004% bromophenol blue, and 0.125 M Tris-HCl) and boiled for 10 min at 95°C for SDS-PAGE electrophoresis. After separation in SDS-PAGE, proteins were transferred to polyvinylidene fluoride membranes (Bio-Rad, Richmond, CA) and probed for different targets with the stated antibodies. Immunoblots were visualized using a chemiluminescence detection system (GE Healthcare, Piscataway, NJ), exposed to Fuji medical X-ray films (Thermo Fisher Scientific), scanned, and analyzed using ImageJ.

Quantitative real-time PCR
Total RNA from rat cortical cultures was purified using TRIzol (Thermo Fisher Scientific; cat. # 12183555) and reverse-transcribed using the SuperScript III Reverse Transcription System (Thermo Fisher Scientific; cat. # 12574035). The optical density A260/A280 ratio was confirmed to be Ͼ1.9 for each sample. For N-cadherin, we used the following oligonucleotides: 5=-ATCATTCGCCA AGAGGAAGG-3= and 5=-GGCTGAAAATAGACCCTGT GA-3=. Quantitative real-time PCR was performed with a 7300 real-time PCR system (Applied Biosystems, Foster City, CA) using Power SYBR Green Master Mix (Applied Biosystems; cat. # 4367659) with the following PCR conditions: initial hold at 95°C for 10 min, followed by 40 cycles of a 15-s denaturing step at 95°C and a 60-s annealing and extension step at 60°C. Transcript levels were normalized to the housekeeping gene GAPDH using the following oligonucleotides: 5=-CCATCAACGACC CCTTCATT-3= and 5=-CTGAGAATGGGAAGCTGGTC-3=.

Cell-surface protein biotinylation assay
Cortical neurons were rinsed with ACSF once and incubated with EZ Link-Sulfo-NHS-LC-Biotin (Thermo Fisher Scientific; cat. # 21327) dissolved in 1 ACSF (1 mg/ml) for 10 min at room temperature and another 20 min at 4°C. Excess biotin reagent was quenched with two washes of ACSF with 20 mM glycine followed by another two washes with ACSF. Neurons were then lysed in lysis buffer 1 (1ϫ PBS with 0.5% SDS, 0.5% sodium deoxycholate, and 1% Triton X-100) with the addition of a protease inhibitor cocktail (Roche, Basel, Switzerland; cat. # 04693116001), sonicated, then head-to-toe rotated at 4°C for 30 min to achieve thorough cell lysis. After spinning down at 13,000 rpm for 15 min, one tenth of the supernatant volume was mixed with an equal volume of Laemmli 2ϫ sample buffer, boiled for 10 min at 95°C, and saved as a total lysate control. The rest of the supernatant was removed to a new Eppendorf 1.5-ml tube containing 40 l of pre-equilibrated NeutrAvidin beads (Thermo Fisher Scientific; cat. # 29200), and the pellet was discarded. NeutrAvidin beads, along with the supernatant, were head-to-toe rotated at 4°C for at least 2 h. The beads were rinsed three times in PBS (with 0.5% Triton X-100), before being mixed with an equal volume of Laemmli 2ϫ sample buffer and boiled for 10 min at 95°C in preparation for WB analysis.

Fluorescence after photobleaching
Images were taken with a Zeiss LSM 700 laser scanning confocal microscope. The inverted microscope was equipped with an incubation system featuring temperature and CO 2 control. All experiments were performed at 37°C and 5% CO 2 . Live images were acquired using a 63ϫ oil-immersion objective lens (NA 1.32).
FRAP experiments were performed using the following protocol: three single prebleach scans were acquired at 3-s intervals, followed by up to five bleach scans at full laser power until the fluorescence reached 25% of the original prebleach levels, over a circular area of 4 m in diameter. During the postbleach period, scans were acquired at 3-s intervals.
Fluorescence was quantified using the FRAP plugin in ImageJ. Background fluorescence was measured in a random field outside of the region of interest (ROI) and subtracted from all the measurements. Growth cone fluorescence was determined for each image and normalized to the initial prebleach fluorescence to determine the rate of fluorescence recovery.
The net fluorescence recovery (mobile fraction, M f ) measured in the region of interest was determined as where F end is the ROI mean intensity at steady state, F post is ROI intensity postbleach, and F pre is mean ROI intensity prebleach.

RhoA activation assay
RhoA activity was assessed using a RhoA Activation Assay Biochem Kit according to the manufacturer's instructions (Cytoskeleton; cat. # BK036). Briefly, GTP-RhoA was immunoprecipitated from whole-cell lysates with glutathione S-transferase-tagged Rhotekin bound to glutathione agarose beads. The beads were washed, and immunoprecipitates were analyzed by WB using a RhoAspecific monoclonal antibody. The lysate was also probed for total RhoA, and GTP-RhoA was normalized to total RhoA levels.

Statistical analyses
An unpaired Student's t-test or one-way ANOVA with post hoc Tukey's test was used as appropriate.

KIDLIA shows nuclear localization and neuronspecific expression in vivo
In situ hybridization studies have shown a lack of KIDLIA mRNA in proliferating, bromodeoxyuridine-positive cells, indicating that it may be expressed in postmitotic neurons only (Cantagrel et al., 2009); however, KIDLIA protein expression has not been examined in neurons. By immunostaining KIDLIA in brain slices from P0 (day of birth) mouse cortex, we observed an exclusive nuclear localization of KIDLIA that colocalized with the nuclear marker Hoechst (Fig. 1A). To further investigate the KIDLIA expression pattern in cortical layers in vivo, we compared the KIDLIA distribution in embryonic day 17 (E17) and P0 mouse brains. In E17 brain slices, KIDLIA was not expressed in the ventricular zone (VZ) or intermediate zone (IZ). Up from the VZ, only minimal background staining of KIDLIA protein was detected until the subplate (SP) region, where KIDLIA expression levels were sharply increased and maintained throughout the entire cortical plate (CP) (Fig. 1B). Similarly, immunostaining of P0 brains showed that strong KIDLIA expression was restricted to the CP in contrast to the VZ/IZ area (Fig. 1C). To determine whether KIDLIA was preferentially expressed between neurons and glia, we coimmunostained KIDLIA with the neuron-specific marker NeuN or the glial marker GFAP. We found that immunofluorescent signals of KIDLIA completely colocalized with NeuN-positive neurons at P0 and P14 (Fig. 1D, E), but not with GFAPpositive glia (P14; Fig. 1F), indicating that KIDLIA expression was neuron specific.

In utero knockdown of KIDLIA regulates neuronal migration without affecting the multipolar-to-bipolar transition
To investigate KIDLIA's role in neuronal migration, we used IUE to knock down KIDLIA expression during early development. KIDLIA shRNA-GFP or a scrambled control was electroporated into mouse embryonic brains at E15 and returned to the pregnant dam to develop ( Fig. 2A). Brains were first collected at E17 and immunostained for KIDLIA. In GFP-positive shRNA electroporated neurons, KIDLIA expression was significantly reduced compared with scrambled controls and nearby nonelectroporated neurons (Fig. 2B).
Callosal projecting pyramidal neurons are born around E15 in the VZ and migrate to their final location in layers II/III in the CP. At E17, 60% of the neurons electroporated with scrambled shRNA were found in the IZ, and only 13% had entered the CP. Strikingly, after electroporation of KIDLIA shRNA, 44% of the neurons were found in the IZ and 28% of the neurons had already migrated into the CP (Fig. 2C, D). These results strongly indicate that loss of KIDLIA expression alters the migration process in the developing brain.
To investigate the effect of KIDLIA on neuron migration at a later stage, we next collected brains at P0 after IUE at E15. In agreement with our findings at E17, we found that 79% of KIDLIA-shRNA neurons had already reached the upper CP at P0, compared with only 64% in scrambled controls. Additionally, in shRNA electroporated brains, only 5% of neurons were found in the IZ compared with 15% in scrambled control brains (Fig. 2E, F). Interestingly, although KIDLIA knockdown resulted in changes in the relative layer distribution of the migrating neurons, it did not affect their final laminar destination, with the majority of the electroporated neurons residing in layer II/III (Fig. 2E).
After birth in the VZ, multipolar pyramidal neurons move within the IZ/SP, where they must adopt a bipolar morphology to enter the CP. This multipolar-to-bipolar transition is key to proper migration and integration of neurons into the cortical plate. KIDLIA proteins begin to be expressed in the SP region below the cortical plate at E17 and may be involved in neuronal migration. We therefore wanted to know whether loss of KIDLIA expression resulted in neurons bypassing the multipolar stage, allowing them to move into the CP directly. In mice electroporated with KIDLIA shRNA at E15, we found that in E17 brains both KIDLIA shRNA and scrambled control neurons showed a typical multipolar morphology in the IZ/SP region. Similar to controls, KIDLIA knockdown neurons showed a normal bi-polar morphology after entering the CP (Fig. 2G, H). These findings suggest that KIDLIA does not affect multipolar-tobipolar transition during neuronal migration.

Knockdown of KIDLIA affects apical dendrite orientation in vivo
To examine the role of KIDLIA in neuronal development, we analyzed dendritic growth and soma location of neu- New Research rons after IUE of KIDLIA shRNA at E15. At P4, neurons have reached their proper laminar location at layer II/III, but the somas of neurons electroporated with KIDLIA-shRNA were located closer to the pial surface (Fig. 3A, C), possibly as a result of a facilitated migration rate or a disruption in the termination of migration. Similar to scrambled controls, neurons with KIDLIA shRNA showed a clear apical dendrite growing as single straight process directed orthogonally to the pial surface (Fig. 3A, B). However, neurons expressing KIDLIA shRNA had a longer apical neurites (Fig. 3A, D). The percentage of cells whose apical neurites reached the pia was not significantly different from controls at P4 (Fig. 3E). Strikingly, brains analyzed at P14 showed that electroporation of KIDLIA shRNA significantly disrupted the orientation of the apical dendrite. The apical dendrites of neurons after KIDLIA knockdown were largely disorganized and not directed toward the pia, compared with age-matched controls (Fig. 3F, G). A significant increase and variation in the angle of the apical dendrite to the pia was observed in KIDLIA shRNA electroporated brains compared with scrambled controls (Fig. 3H). KIDLIA knockdown also produced a 35% decrease in the length of the major apical dendrite and a significant decrease in the distance of their somas to the pia (Fig. 3I, J). Additionally, after KIDLIA knockdown, the number of dendrite tips that reached the pia was significantly decreased compared with controls (Fig. 3K), presumably owing to a disorganization of the apical dendrite orientation and decreased dendritic growth. These in vivo results showed that after knockdown of KIDLIA, neuronal somas were positioned at sites closer to the pial surface at both P4 and P14. A loss of KIDLIA caused aberrant dendrite orientation and decreased apical dendrite growth, indicating that the directed outgrowth and branching of the dendritic tree was significantly impaired, possibly as a consequence of the neurons' early arrival into the CP or a subtle shift in laminar localization.

Knockdown of KIDLIA decreases dendritic outgrowth in primary cultured neurons
To further investigate the molecular mechanisms underlying the effect of KIDLIA on dendritic growth and arborization, we suppressed KIDLIA expression in primary cultured neurons. We infected cortical neurons at the time of plating (DIV0) with lentiviral shRNA containing the same targeting sequences as those used for IUE in vivo and found a ϳ60% reduction in KIDLIA protein expression 6 d after infection (Fig. 4A, B). Consistent with the in vivo observations, we confirmed a similar nuclear localization of KIDLIA in cultured neurons (Fig. 4A, C).
To investigate the effect of KIDLIA knockdown on dendritic outgrowth, we infected neurons with KIDLIA shRNA virus at DIV0 and immunostained for MAP2 and tau1 at DIV12 to label the dendrite and axon, respectively (Fig.  4D). Strikingly, Sholl analysis revealed a large decrease in dendritic branching after KIDLIA knockdown (Fig. 4E). Compared with scrambled controls, we observed a ϳ25% reduction in the length of the longest dendrite, a nearly 50% reduction in the number of dendritic branches, and a 55% reduction in total dendritic length ( Fig. 4F-H). These results show that loss of KIDLIA expression severely stunted neuronal development in vitro.

Knockdown of KIDLIA leads to an increase in surface N-cadherin/␦-catenin association
N-cadherin, the neural member of the cadherin superfamily, has been shown to be involved in neurite outgrowth (Bard et al., 2008). N-cadherin is structurally composed of five extracellular cadherin domains, a single-pass transmembrane domain, and an intracellular domain that interacts with catenins that regulate downstream signaling cascades including the Rho GTPases.
A previous study indicated that in PC12 cells, knockdown of KIDLIA upregulates the expression of N-cadherin (Magome et al., 2013). We therefore sought to investigate whether knockdown of KIDLIA affected N-cadherin expression and localization in neurons. In DIV6 neurons that were infected with KIDLIA shRNA at DIV0, we found that KIDLIA knockdown led to a ϳ25% increase in N-cadherin protein levels compared with scrambled controls (Fig. 5A, B). Because KIDLIA is localized in the nucleus, we next examined whether KIDLIA regulates N-cadherin gene transcription. We infected DIV0 cultured cortical neurons with KIDLIA shRNAs for 7 d and measured N-cadherin mRNA by RT-PCR using the cell lysates. After knockdown of KIDLIA, we found a 35% increase in N-cadherin mRNA compared with scrambled shRNA and untreated controls (Fig. 5C). These data suggest that the KIDLIA-induced increase in N-cadherin protein amount may result from an upregulation in its gene transcription and translation.
To assess the membrane localization of N-cadherin after KIDLIA knockdown, we isolated cell-surface proteins through biotinylation and immunoprecipitation with sulfo-NHS-SS-biotin. Surprisingly, we found a greater than twofold increase in surface N-cadherin levels after shRNA-mediated knockdown of KIDLIA compared with scrambled controls (Fig. 5D, E), indicating that KIDLIA knockdown not only increased overall N-cadherin expression, but also caused a translocation from the cytosolic compartment to the cell surface.
␦-Catenin is a critical functional mediator for N-cadherin via a direct protein association. ␦-Catenin expression can induce a dendritic-like morphology in fibroblasts (Yu and Malenka, 2003) and stimulates neurite outgrowth in hippocampal neurons (Martinez et al., 2003). Importantly, an increase in membrane-localized N-cadherin suppresses the growth-promoting effects of ␦-catenin, suggesting that surface N-cadherin acts as a buffer regulating cytosolic ␦-catenin availability (Kim et al., 2008). Given that ␦-catenin is brain specific (Abu-Elneel et al., 2008), and that its localization and ability to induce neurite outgrowth are tightly linked with N-cadherin, we hypothesized that the increased membrane expression of N-cadherin sequesters ␦-catenin at the surface and thus depletes its cytosolic pool.
To investigate this hypothesis, we performed coimmunoprecipitation studies using lysates of DIV6 cultured cor- ). An angle of 0°indicates that a dendrite is growing directly toward the tical neurons infected with viral KIDLIA shRNAs. We found that knockdown of KIDLIA significantly enhanced the association of N-cadherin with ␦-catenin. Meanwhile, we observed a major reduction in the amount of free unbound ␦-catenin in the supernatant after immunoprecipitation (Fig. 5F). These results indicate that loss of KIDLIA results in an increase in the association of N-cadherin with ␦-catenin at the plasma membrane, resulting in a reduction in free cytosolic ␦-catenin.

␦-Catenin is involved in KIDLIA-dependent changes in neurite growth and arborization
Because free cytosolic ␦-catenin is required for its downstream signaling, we next examined whether over-expression of ␦-catenin after loss of KIDLIA could rescue the deficits in neurite outgrowth and branching. Neurons were treated with scrambled or KIDLIA lentiviral shRNA at DIV0 and transfected with ␦-catenin-GFP or GFP control 1 d later (Fig. 5G). At DIV6, Sholl analysis revealed a large decrease in dendritic branching in shRNA ϩ GFP cells compared with scrambled ϩ GFP. However, in neurons overexpressing ␦-catenin-GFP ϩ shRNA, neurite branching was restored to levels similar to scrambled controls (Fig. 5H). These results strongly indicate that the decrease in neurite outgrowth and branching after knockdown of KIDLIA was caused by a reduction in free ␦-catenin availability.

Loss of KIDLIA disrupts actin dynamics at the neurite growth cone
Actin is dynamically regulated at the neurite tips, which plays a crucial role in neurite growth (Meberg and Bamburg, 2000;Nicholson-Dykstra et al., 2005). To examine whether KIDLIA is implicated in cytoskeletal dynamics, we performed FRAP experiments with fluorescently labeled actin after knockdown of KIDLIA with siRNA. To test the efficacy of the KIDLIA knockdown, scrambled or KIDLIA siRNA was cotransfected with GFP at DIV0, and immunostainings of KIDLIA at DIV4 showed a ϳ60% reduction in protein expression (Fig. 6A, B). Next, GFP-actin was transfected at DIV0 into hippocampal neurons with scrambled or KIDLIA siRNA, and FRAP was performed on the growth cones at DIV4 (Fig. 6C). In neurites from KIDLIA siRNA-transfected neurons, the recovery rate of the actin signal was drastically reduced (Fig. 6D). Compared with scrambled siRNA controls, KIDLIA knockdown showed a 70% decrease in the mobile fraction (M f ) of actin (Fig. 6G) and a subsequent increase in the immobile fraction (IM f ) of actin (Fig. 6H).
Because of the large reduction of free ␦-catenin in the cytosol after KIDLIA knockdown, which is known to be involved in actin regulation, we next sought to examine whether overexpression of ␦-catenin could rescue actin dynamics with the transfection of ␦-catenin-GFP after siRNA-mediated knockdown of KIDLIA (Fig. 6E). Indeed, FRAP revealed that in ␦-catenin-transfected neurons, actin dynamics were restored (Fig. 6F) and the mobile and immobile fractions of actin returned to levels similar to those of controls (Fig. 6G, H), indicating that the impaired actin dynamics likely resulted from a reduction of free cytoplasmic ␦-catenin.

Role for RhoA in the KIDLIA-dependent impairment of actin dynamics
A major downstream effector of ␦-catenin is the Rho-GTPase pathway, which links the cadherin/catenin complex to actin dynamics. RhoA GTPase activation leads to an inhibition in neurite growth (Kozma et al., 1997;Leeuwen et al., 1997). Studies have shown that free cytosolic ␦-catenin, but not the membrane-associated fractions, inhibits RhoA activity (Kim et al., 2008). Because KIDLIA regulates the association of ␦-catenin to surface N-cadherin and thus reduces the availability of cytosolic ␦-catenin, we wanted to know whether KIDLIA knockdown affected RhoA activity. Rho activity status alternates between an active, GTP-bound state and an inactive, GDP-bound state. To perform RhoA activity assays, we infected neurons with lentivirus containing scrambled or KIDLIA shRNA. Neuron lysates were incubated with a GST fusion protein containing the binding domain of the Rho effector protein rhotekin, so that the active form of RhoA was isolated by immunoprecipitation. We then probed for total RhoA in lysates and the immunoprecipitated active RhoA via WB (Fig. 7A). Interestingly, we found that KIDLIA knockdown led to a 60% increase in the amount of active RhoA compared with scrambled controls (Fig. 7B). Because RhoA activation prevents neurite initiation and induces neurite retraction, our findings suggest that the inhibitory effect of KIDLIA knockdown on dendrite growth may be mediated by RhoA.
To further determine the role of RhoA activity in the KIDLIA-dependent effects on neuron development, we first performed FRAP experiments to examine the actin dynamics with the application of CN06, which directly inhibits the primary RhoA effector ROCK (Ishizaki et al., 2000). In KIDLIA knockdown neurons, application of CN06 1 h before FRAP was sufficient to rescue the actin dynamics to levels similar to those of scrambled controls (Fig. 7C, D). Furthermore, we wanted to determine whether the RhoA signaling pathway was responsible for the KIDLIA-dependent impairment in dendritic arborization. We therefore infected neurons with KIDLIA shRNA virus at DIV0 followed by CN06 treatment from DIV4 to DIV7. Dendritic structure indicated by MAP2 staining was examined via Sholl analysis. Indeed, after KIDLIA knockdown in neurons, we found that CN06 incubation rescued the defects in dendritic growth and branching (Fig. 7E, F). These findings establish a molecular process in which KIDLIA knockdown induces an increase in membranebound N-cadherin and sequestration of cytosolic ␦-catenin, leading to activation of the RhoA pathway and a subsequent alteration in actin dynamics, eventually causing suppression in neurite growth and branching (Fig. 7G).

Discussion
Our study provides the first evidence showing that KIDLIA, the protein product of the recently identified XLID gene KIAA2022, plays an important role in neuron migration and morphogenesis. In mouse brain, knockdown of KIDLIA results in a redistribution of more neurons in the cortical plate at earlier time points and a subtle, but potentially consequential, mislocalization of neurons within their destined cortical layers. In addition, we find that early growth of the leading apical neurite is positively regulated in KIDLIA knockdown neurons; however, at a later time point (P14), loss of KIDLIA causes an inhibition in apical dendrite growth and a disruption of dendritic orientation. Given that IUE transfects only a small portion of neurons derived at a specific time and the majority of the neighboring neurons remain unaffected, the effects of KIDLIA are likely neuron autonomous, rather than being caused by external environmental factors.
How neuron migration is regulated by KIDLIA remains to be investigated. KIDLIA protein expression was mostly restricted to the cortical plate, with a distinct band of expression turning on in the subplate region just before the CP at E17 in mouse brain. IUE of KIDLIA shRNA led to more neurons migrating to upper cortical layers with a closer positioning of the soma to the pia. After migration, neurons reached their proper laminar layers; however, the aberrant positioning of the soma relative to the pia may indicate a disruption in the termination of the migration processor the final somal translocation after migration to layer II/III. However, we observed no change in the multipolar transition phase before entry into the CP. Future studies using in utero electroporation of KIDLIA shRNA at E12.5 to label layer V/VI neurons would be useful to investigate whether loss of KIDLIA could mislocalize deeper-layer neurons to upper cortical layers. Additionally, aberrant soma positioning could be due to premature cell cycle exit during proliferation, resulting in an earlier arrival of neurons to their destined cortical layers. The distinct expression pattern of KIDLIA within and just below the CP in embryonic brains suggests that KIDLIA may Regions at the growing neurite tip were selected for photobleaching at 488 nm and imaged every 3 s. D, Analysis of the FRAP data showed that knockdown of KIDLIA produced a dramatic decrease in actin dynamics after photobleaching (n ϭ 9). E, Neurons were cotransfected with KIDLIA siRNA or scrambled siRNA with actin-mCherry and ␦-catenin-GFP or GFP alone, photobleached at 555 nm, and imaged every 3 s. F, Analysis of the FRAP data. Overexpression of ␦-catenin rescued the actin dynamics after knockdown of KIDLIA (n ϭ 7). G, The mobile fraction, calculated as the difference between the average level of bleaching and the level of recovery, was significantly decreased after knockdown of KIDLIA (n ϭ 7). H, The immobile fraction of actin, calculated as the difference between the initial fluorescence and the level of recovery, was significantly decreased (n ϭ 7). ‫‪p‬ءء‬ Ͻ 0.01, ‫‪p‬ءءءء‬ Ͻ 0.0001. Error bars ϭ SEM. act as a checkpoint factor for CP entry; a loss of KIDLIA would therefore offer neurons free access to pass the IZ-CP border and enter into the CP. We have observed similar changes in neurite growth in cultured neurons. KIDLIA knockdown led to a significant reduction in dendrite length and complexity. Using this in vitro system, we investigated the cellular mechanisms responsible for the disrupted dendritic development. We found that loss of KIDLIA induced an increase in total N-cadherin levels, with a substantial increase in the surfaced-localized fraction, which was accompanied by an elevated association of surface N-cadherin with ␦-catenin. The increased ␦-catenin/N-cadherin association led to depletion of the free cytosolic pool of ␦-catenin, thereby increasing the activation of the downstream RhoA pathway. The RhoA pathway is a major mediator of actin dynamics and neurite outgrowth and complexity. Extensively branched processes can be induced when RhoA is inhibited via ␦-catenin. Conversely, when RhoA is activated, dendrite length and the dendritic field are decreased (Li et al., 2000;Nakayama et al., 2000;Wong et al., 2000). The reduction in ␦-catenin availability is responsible for the KIDLIA-dependent effect on dendrite morphogenesis, because overexpression of ␦-catenin rescued neurite growth and dendritic branching as well as actin dynamics in neurons after KIDLIA knockdown. In line with our findings that ␦-catenin is a key mediator for the neuronal effects of KIDLIA, ␦-catenin was identified as a major genetic target in the autism population (Turner et al., 2015). Interestingly, of the autism genes positively correlated with ␦-catenin, there is a significant enrichment in genes involved in dendrite morphogenesis, including PDLIM5, SHANK1, CDKL5, and DLG4 (Turner et al., 2015). In addition, loss of ␦-catenin is implicated in impaired cognitive function and intellectual disabilities (Medina et al., 2000;Belcaro et al., 2015;Hofmeister et al., 2015), indicating a crucial role for ␦-catenin in brain development and function.
Under the condition of KIDLIA knockdown, we found an increase in N-cadherin protein levels and an elevated association between N-cadherin and ␦-catenin, but the underlying mechanism remains unclear. It is possible that a lack of KIDLIA expression in the nucleus leads to upregulation in N-cadherin gene transcription and subsequent protein translation. Regarding KIDLIA-induced changes in protein interaction, it has been shown that ␦-catenin is subject to protein palmitoylation (Kang et al., 2008), a modification that causes enhanced association of ␦-catenin with N-cadherin (Brigidi et al., 2014). Also, by binding to the juxtamembrane domain of cadherin, ␦-catenin is known to stabilize and increase the amount of N-cadherin at the surface (Reynolds and Carnahan, 2004). It is thus conceivable that a loss of KIDLIA may cause ␦-catenin palmitoylation, possibly via enhancing the expression of the palmitoyl-acyl transferase DHHC5 (Brigidi et al., 2014), leading to higher levels of association between ␦-catenin and N-cadherin.
We found that the N-cadherin/␦-catenin effect is mediated by RhoA. The Rho GTPases regulate dendrite growth and branching via modulation of cytoskeleton compo-nents (Newey et al., 2005). The role for RhoA in dendritic branching has recently been established, as RhoA activation leads to a reduction in dendritic branching (Nakayama et al., 2000), whereas RhoA inhibition enhances branching (Neumann and Schweigreiter, 2002). Cytoplasmic ␦-catenin has previously been shown to inhibit RhoA by keeping it in the inactive RhoA-GDP state, resulting in an increase in dendritic branching (Martinez et al., 2003). Constitutively active RhoA expression has been shown to reduce dendrite length and the volume of the dendritic field (Nakayama et al., 2000;Wong et al., 2000), whereas RhoA loss-of-function mutations have also been shown to cause abnormal dendritic arborization (Lee et al., 2000).
RT-PCR of mRNA prepared from prenatal and postnatal mouse brain shows a sevenfold increase in KIDLIA expression between E10.5 and E18.5, indicating a role for KIDLIA in neural development. KIDLIA mRNA expression reaches a maximum at P3 and is maintained at a low level into adulthood (Cantagrel et al., 2004;Ishikawa et al., 2012). Thus, KIDLIA expression peaks during key developmental time periods for neuronal growth and maturation. In both in vivo in mouse brain and cultured neurons, immunostainings reveal colocalization of KIDLIA with the nuclear marker Hoechst. KIDLIA is a large 170-kDa protein with monopartite and bipartite nuclear localization sequences. Given the specific nuclear localization, we suspect a major role for KIDLIA in gene regulation. It is possible that KIDLIA knockdown causes upregulation in N-cadherin gene transcription and thus an elevated amount of N-cadherin.
Attenuated growth and structural abnormalities in developing neurons lead to deficiencies in neuronal wiring and synapse formation during brain maturation. Aberrant neuron morphogenesis and synaptogenesis are associated with a number of brain disorders, including fragile-X mental retardation, Rett syndrome, Down syndrome, and CDKL5-related encephalopathy (Belmonte and Allen, 2004;Shepherd and Katz, 2011;Garner and Wetmore, 2012;Ricciardi et al., 2012). Given that KIDLIA is a novel gene with largely unknown functions, more studies are needed to elucidate the role of KIDLIA in multiple steps of neuron development including neurogenesis, morphogenesis, synapse maturation, synaptic plasticity, and behavior.