MicroRNA-214 Promotes Dendritic Development by Targeting the Schizophrenia-associated Gene Quaking (Qki)*

Proper dendritic elaboration of neurons is critical for the formation of functional circuits during brain development. Defects in dendrite morphogenesis are associated with neuropsychiatric disorders, and microRNAs are emerging as regulators of aspects of neuronal maturation such as axonal and dendritic growth, spine formation, and synaptogenesis. Here, we show that miR-214 plays a pivotal role in the regulation of dendritic development. Overexpression of miR-214 increased dendrite size and complexity, whereas blocking of endogenous miR-214-3p, a mature form of miR-214, inhibited dendritic morphogenesis. We also found that miR-214-3p targets quaking (Qki), which is implicated in psychiatric diseases such as schizophrenia, through conserved target sites located in the 3′-untranslated region of Qki mRNA, thereby down-regulating Qki protein levels. Overexpression and knockdown of Qki impaired and enhanced dendritic formation, respectively. Moreover, overexpression of Qki abolished the dendritic growth induced by miR-214 overexpression. Taken together, our findings reveal a crucial role for the miR-214-Qki pathway in the regulation of neuronal dendritic development.

Neurons are highly polarized cells composed of the following two structurally and functionally distinct processes: the axon, which relays information to other neurons, and the dendrites, which receive information inputs from other neurons (1). The dendrites are the primary site in neurons where synapse formation and signal integration occur, with dendrite size and the extent of arborization determining the number and distribution of innervating axons and functional synapses (2,3). Because dendrites play a critical role in defining the synaptic input, regulation of their growth is profoundly important for the establishment of functional neuronal networks (4,5). Consequently, impaired dendritic growth is associated with a broader class of neurodevelopmental disorders, including psy-chiatric diseases (6). However, the mechanisms governing dendritic growth remain to be fully elucidated.
MicroRNAs (miRNAs) 3 are small noncoding RNAs that function as modulators of gene expression at the post-transcriptional level and thereby influence many biological processes, including cellular proliferation, differentiation, and apoptosis. Primary miRNAs (pri-miRNAs) are transcribed from DNA and are processed into precursor miRNAs (pre-miRNAs) by the Drosha complex in the nucleus. The pre-miRNAs are transported from the nucleus to cytoplasm and are processed into mature miRNAs by Dicer. Mature miRNAs bind to the 3Ј-untranslated region (3ЈUTR) of target mRNAs and negatively regulate gene expression by inhibiting translation or mRNA degradation (7,8). Recent studies have shown that miRNAs act as regulators of neurodevelopment and dysregulation, which may contribute to neurological disorders (9,10). For example, miR-9 negatively regulates axonal growth and branching by targeting microtubule-associated protein 1b mRNA (11), and miR-138 restricts the size of dendritic spines through the regulation of acyl protein thioesterase 1 (12), whereas miR-137 inhibits dendritic morphogenesis by regulating the level of Mind bomb1 protein translation (13).
miR-214 functions in various cell types, promoting myogenic differentiation of C2C12 cells by targeting N-ras (14) and upregulating the expression level of Nanog by targeting p53 to regulate ovarian cancer cell stemness (15). miR-214 has also been shown to act as a regulator of cardiomyocyte Ca 2ϩ homeostasis and survival (16) and to promote neurite outgrowth during differentiation of neuroblastoma cells (17). However, the role of miR-214 in neuronal development remains elusive.
In this study, we show that miR-214 plays a key role in dendritic morphogenesis of hippocampal neurons. Overexpression and blocking of miR-214 promoted and inhibited dendrite development, respectively. In addition, we identified the mRNA of the quaking gene, called quaking homolog, KH domain RNA binding (Qki), which is implicated in psychiatric disorders (18,19), as a direct target of miR-214-3p. Furthermore, we show that Qki perturbs dendrite formation and that Qki expression abolishes the dendritic phenotypes caused by miR-214 overexpression. These findings reveal a critical role for the miR-214-Qki pathway in the regulation of neuronal development.

Experimental Procedures
Animals-All aspects of animal care and treatment were carried out according to the guidelines of the Experimental Animal Care Committee of Kyushu University. Timed-pregnant ICR mice (Japan SLC) were used in this research.
Lentivirus Production-Lentiviruses were produced as described previously (23). Briefly, lentiviruses were generated by co-transfecting HEK293T cells with the lentivirus vector constructs pCMV-VSV-G-RSV-Rev and pCAG-HIVgp using polyethyleneimine (Polysciences). The culture supernatants were collected 48 h after transfection, and virus was introduced into neurons by adding these supernatants to the culture media.
In Utero Electroporation-To evaluate dendritic growth in vivo, in utero electroporation was performed on E14 mouse embryos as described previously (24). Briefly, plasmid DNA (0.1 g/l in PBS containing 0.1% Fast-Green) was injected (0.5-1 l) into the lateral ventricle of the embryonic brain from outside the uterus with a glass micropipette (GD-1, Narishige). Holding the embryo in the uterus with forceps-type electrodes (NEPA GENE), 50-ms electric pulses of 45 V were delivered five times at intervals of 950 ms using a model CUY21 Single Cell Electroporator (Nepa Gene). Glass micropipettes were prepared using a P-1000IVF (Sutter). Animals were perfused with 4% paraformaldehyde at postnatal day 10 (P10). Collected brains were postfixed with 4% paraformaldehyde overnight at 4°C and then equilibrated in 30% sucrose. Brains were frozen at Ϫ80°C after embedding in optimal cutting temperature compound (Sakura Finetek) and serially sectioned at 40-m thickness.
Immunocytochemistry-Cells were fixed at the indicated day(s) in vitro (DIV) with 4% paraformaldehyde in phosphatebuffered saline (PBS), washed with PBS, permeabilized, and blocked with blocking buffer (3% FBS and 0.1% Triton X-100 in PBS) at room temperature. The cells were then incubated with primary antibody solution at room temperature for 3 h. After being washed with PBS, the cells were incubated with secondary antibody solution at room temperature for 1 h, and after further washing with PBS, they were mounted on glass slides.
Immunohistochemistry-Sections were washed with PBS, permeabilized, and blocked with blocking buffer at room temperature. The sections were incubated with primary antibody solution overnight at 4°C. After being washed with PBS, the sections were incubated with secondary antibody solution at room temperature for 2 h. After being washed with PBS, the sections were mounted on glass slides. Fluorescence images were acquired using a Zeiss LSM 700 confocal microscope with a ϫ20 objective lens. Z series of 20 images were taken at 1-m intervals at a 1024 ϫ 1024-pixel resolution.

miR-214 Regulates Dendrite Development by Targeting Qki
Immunoblotting-Cells were lysed with a buffer containing 0.5% Nonidet P-40, 10 mM Tris-HCl, pH 7.5, 150 mM NaCl, and 1% protease inhibitor mixture (Nacalai Tesque). Lysates were sonicated and centrifuged at 20,000 ϫ g for 15 min at 4°C. Total cell lysates were subjected to SDS-PAGE and transferred to a PVDF transfer membrane (GE Healthcare). The blots were blocked with 0.3% skim milk in TBST (50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 0.1% Tween 20), and after incubation with a primary antibody, they were washed with TBST and incubated with a peroxidase-conjugated secondary antibody. Immunoreactive bands were detected by enhanced chemiluminescence using ECL Prime Western blotting detection reagent (GE Healthcare).
Morphological Analysis of Cultured Hippocampal Neurons-For analysis of neurite development, hippocampal neurons were subjected to immunocytochemistry using anti-Tuj-1 and anti-GFP antibodies at 3DIV. Tuj-1-positive neurite length was measured using ImageJ software.
To analyze axon development, hippocampal neurons were subjected to immunocytochemistry using anti-Tau-1 and anti-GFP antibody at 3DIV. Neurites with a strong Tau-1 signal at their proximal end were counted as axons. Axon length and branch number were measured using ImageJ.
For analysis of dendrite development in vitro, hippocampal neurons were subjected to immunostaining with antibodies against MAP2 and GFP at 6DIV. Dendrites were defined as MAP2-positive neurites. Sholl analysis and quantification of dendritic length and branch number were performed using ImageJ software. For Sholl analysis, concentric circles having 10-m increments in radius were defined from the center of the cell body. The number of MAP2-positive dendrites crossing each circle was counted. The total number of crossings for each cell was measured as an index for total dendritic complexity as described previously (25).
For in vivo dendrite analysis, brain sections were subjected to immunohistochemistry with anti-GFP antibody. Total dendritic length and branch number of GFP-positive neurons in layer 4 were measured using ImageJ. For Sholl analysis, concentric circles having 10-m increments in radius were defined from the center of the cell body. The number of GFP-positive dendrites crossing each circle was counted. The total number of crossings for each cell was calculated as an objective measurement of total dendritic complexity.
qRT-PCR-qRT-PCR analysis was performed to measure the expression levels of primary and mature miRNAs, as described previously (26). In brief, total RNAs were extracted with TRIzol (Invitrogen) and subjected to reverse transcription with the SuperScript VILO cDNA synthesis kit (Invitrogen) according to the manufacturer's protocol. qRT-PCR was performed with the StepOne real time PCR system (Applied Biosystems). To detect primary and mature miRNAs, a TaqMan microRNA assay kit (Applied Biosystems) was used in accordance with the manufacturer's protocol. Data analysis was performed using the comparative Ct method. Results were normalized to Gapdh or U6 snRNA.
Statistical Analysis-The results presented are the average of at least three experiments, each performed in triplicate, with standard errors. Statistical analyses were performed by oneway ANOVA, followed by Tukey's multiple comparison tests or by Student's t test, as appropriate, using Prism 5 (GraphPad Software). Probabilities of p Ͻ 0.05 were considered significant.

Structure and Expression of miR-214 -miR-214
is an intragenic microRNA encoded in the mouse dynamin 3 (Dnm3) gene, located on the opposite strand in the 14th intronic region (14). miR-214 is transcribed together with miR-199a-2 as an antisense RNA of Dnm3 (Dnm3os) on mouse chromosome 1, and the two mature forms of miR-214, miR-214 -5p and miR-214-3p, are highly conserved across mammalian species (Fig.  1A). To explore possible roles of miR-214 in neuronal development, we first investigated expression levels of miR-214 in the mouse brain by qRT-PCR analysis. Although regional variation was observed, substantial expression of miR-214 was confirmed in P1 mouse brain (Fig. 1B). We also measured the level of miR-214 in developing cultured neurons derived from E17.5 hippocampi. The expression level of primary miR-214 transiently increased at an early stage in cultured hippocampal neurons and then declined at later stages (Fig. 1C). However, mature miR-214 levels gradually increased during neuronal miR-214 Regulates Dendrite Development by Targeting Qki maturation (Fig. 1D), suggesting that miR-214 plays some role in neuronal development.
miR-214 Promotes Dendritic Development of Hippocampal Neurons-To investigate the function of miR-214 in neurons, we next expressed miR-214 in primary cultured E17 hippocampal neurons by infecting them with lentiviruses expressing GFP as control or GFP together with miR-214 ( Fig. 2A), and we evaluated axonal and dendritic morphologies. Overexpression of miR-214 was confirmed by qRT-PCR (Fig. 2B). We found that overexpression of miR-214 in hippocampal neurons significantly increased total dendrite length and dendritic branch numbers compared with control ( Fig. 2, C-E). We also performed Sholl analysis by measuring the number of dendrites that intersect concentric circles at different radial distances from the cell body (Fig. 2F). The results revealed that miR-214expressing neurons exhibited enhanced dendritic complexity compared with control neurons (Fig. 2G). In accordance with this result, the total crossing number was significantly increased by miR-214 overexpression in neurons (Fig. 2H). However, miR-214-expressing neurons did not show any significant change in axonal growth (Fig. 2, I and J). These results suggest that miR-214 promotes dendritic but not axonal development in hippocampal neurons.
miR-214-3p Functions in Dendritic Development-Precursor miR-214 generates two mature miRNAs, miR-214 -5p and miR-214-3p. Therefore, we next examined which mature form of miR-214 regulates dendritic development of neurons. We expressed an miRNA inhibitor (sponge) against each miR-214 -5p and miR-214-3p (Fig. 3A) in hippocampal neurons and evaluated dendrite formation. Blocking of endogenous miR-214-3p significantly decreased both dendritic branch number and length compared with control, although the inhibition of miR-214 -5p did not affect dendritic development (Fig. 3,  B-D). Moreover, inhibition of miR-214-3p but not miR-214 -5p markedly reduced dendritic complexity compared with control (Fig. 3, E and F). We obtained almost the same FIGURE 1. Genomic structure of miR-214 and its expression patterns in the developing brain and hippocampal neurons. A, diagram of the structure of the mouse miR-214 locus and the sequence of miR-214 precursor. pri-miR-214 is transcribed as an antisense RNA of dynamin-3 (Dnm3os) with pri-miR-199a-2. The nucleotide sequences of mature miR-214 -5p and -3p are highly conserved among mammalian species. Highlighted regions indicate the seed sequence. B, mature miR-214 expression levels in P1 mouse brain tissues were measured by qRT-PCR. C and D, expression levels of primary (C) and mature (D) forms of miR-214 were measured by qRT-PCR in cultured developing hippocampal neurons at 0, 1, 3, 6, and 10DIV.

miR-214 Regulates Dendrite Development by Targeting Qki
results by using another inhibitor for miR-214-3p with a different sequence from Sponge-miR-214-3pi-1 (data not shown). Consistent with the gain-of-function experiments, inhibition of neither miR-214 -5p nor miR-214-3p influenced axonal growth (Fig. 3, G and H). These results indicate that miR-214-3p is important for dendritic development in hippocampal neurons.
miR-214-3p Targets Qki in Hippocampal Neurons-To gain further insight into the mechanisms by which miR-214 regulates dendritic development, we attempted to identify downstream target genes of miR-214-3p. We first searched miR-214-3p targets using the public databases miRDB, TargetScan, and PicTar, and 24 candidate target genes, common to all three databases, were identified. To further narrow down plausible target genes, we sought candidate targets that have more than three putative miR-214-3p seed sites in their 3ЈUTR and found that five genes, quaking (Qki), neuronal pentraxin receptor (Nptxr), v-crk avian sarcoma virus CT10 oncogene homologlike (Crkl), hepatoma-derived growth factor (Hdgf), and leucine zipper, down-regulated in cancer 1 (Ldoc1), met this criterion (Fig. 4A). We then performed functional screening for direct miR-214-3p targets by expressing the five genes in hippocampal neurons and evaluating neurite outgrowth after 3 days. To function as a mediator of miR-214-dependent effects on dendritic formation, a downstream target of miR-214-3p should negatively regulate neurite growth. Among the candidate genes, we found that only Qki overexpression significantly suppressed Tuj-1-positive neurite outgrowth (Fig. 4, B and C). To

miR-214 Regulates Dendrite Development by Targeting Qki
further investigate whether miR-214-3p targets Qki in neurons, we generated miRNA reporter constructs in which a luciferase reporter gene was placed under post-transcriptional control of the native Qki 3ЈUTR or of a Qki 3ЈUTR harboring mutations in all three miR-214-3p seed sites (Fig. 4D). These luciferase constructs were co-transfected with a miR-214-expressing plasmid into hippocampal neurons, and luciferase activity was measured 3 days later. The luciferase activity of the native Qki 3ЈUTR construct was significantly decreased by miR-214 expression, whereas the reporter constructs with mutated seed sequences showed no such sensitivity to miR-214 expression (Fig. 4E, left). In contrast, when we performed luciferase assay using the construct with 3ЈUTRs of Crkl and Hdgf, the luciferase activities were not altered by miR-214 expression, sug-gesting that mRNAs of them are not targets of miR-214 (Fig.  4E, middle and right). To determine whether miR-214 regulates expression levels of Qki, we expressed miR-214 and assessed Qki protein levels in neurons by immunoblotting analysis. The Qki gene generates three alternatively spliced isoforms encoding Qki-5, Qki-6, and Qki-7 that differ in their C-terminal 30 amino acids (27). We found that protein levels of all Qki isoforms were significantly decreased in miR-214-overexpressing cells (Fig. 4, F and G). From these observations, we concluded that miR-214-3p directly targets Qki in hippocampal neurons.
Overexpression of Qki Suppresses Dendritic Formation-Qki is an RNA-binding protein belonging to the STAR (signal transduction and activation of RNA) protein family, and it post-

miR-214 Regulates Dendrite Development by Targeting Qki
transcriptionally regulates its mRNA ligands (28). Functional studies of mouse Qki have revealed its role in oligodendrocyte development (28). In humans, QKI is located in a previously identified schizophrenia susceptibility locus on chromosome 6 (29 -33). Furthermore, other studies showed reduced QKI expression in psychiatric diseases such as schizophrenia (34 -36) and major depressive disorders (37), suggesting that QKI has an important role in the pathogenesis of psychiatric disorders, especially of schizophrenia. However, the function of QKI in neurons remains unexplored.
As a first step toward understanding the function of Qki in neurons, we performed a gain-of-function experiment by expressing Qki in hippocampal neurons (Fig. 5A) and evaluating dendritic growth. Overexpression of Qki was confirmed by immunoblotting using an anti-QKI antibody (Fig. 5B). In Qkioverexpressing neurons, total dendrite length and branch numbers decreased compared with control neurons (Fig. 5, C-E). In addition, Sholl analysis indicated that overexpression of Qki reduced the dendritic arborization of neurons (Fig. 5, F and G).
These results indicate that Qki negatively regulates dendritic formation in hippocampal neurons.
Knockdown of Qki Promotes Dendritic Formation-In light of the above results, we next analyzed the effects of Qki down-regulation on neuronal development. Hippocampal neurons were infected with lentivirus expressing short hairpin RNAs (shRNAs) against Qki (sh-Qki-1, -2, and -3) (Fig. 6,  A and B), and dendritic formation was evaluated. We first checked the knockdown efficiency of sh-Qki-1 by immuno-  JUNE 24, 2016 • VOLUME 291 • NUMBER 26 blotting analysis and observed a marked reduction of Qki protein levels following the expression of the shRNA (Fig.  6C). Knockdown of Qki increased dendritic numbers and total dendrite length (Fig. 6, D-F). Dendritic complexity was also increased by Qki knockdown (Fig. 6, G and H). We repeated the same experiments with an additional two shRNAs for Qki (sh-Qki-2 and -3) with different target sequences and obtained almost the same results (Fig. 6, B  and I-N). These results suggest that Qki is important for dendritic elaboration in neurons.

miR-214 Regulates Dendrite Development by Targeting Qki
Qki Acts Downstream of miR-214 in Dendritic Development-If miR-214 influences dendritic development by regulating Qki, expression of Qki should cancel the effects of miR-214. To test this prediction, we co-expressed miR-214 with Qki, either pos-

miR-214 Regulates Dendrite Development by Targeting Qki
sessing or lacking its 3ЈUTR containing three miR-214 target sites, in hippocampal neurons (Fig. 7A) and assessed dendrite morphology. The expression levels of miR-214 and Qki in lentivirus-infected neurons were confirmed by qRT-PCR and immunoblotting, respectively (Fig. 7, B and C). We found that co-expression with Qki abrogated the enhanced dendritic growth induced by the expression of miR-214 (Fig. 7, D-F). The effects of miR-214 on dendritic complexity were also diminished by Qki expression (Fig.   7G). The total number of dendrite crossings in Qki-co-expressing neurons showed abrogation of the increased dendrite complexity by miR-214 expression (Fig. 7H). When Qki possessing its 3ЈUTR sequence (Qki-3ЈUTR) was co-expressed with miR-214, abrogation of miR-214 function in dendritic formation was less effective (Fig. 7, D-H). Together, these data indicate that Qki acts downstream of miR-214 in the regulation of dendritic development in hippocampal neurons.  JUNE 24, 2016 • VOLUME 291 • NUMBER 26

JOURNAL OF BIOLOGICAL CHEMISTRY 13899
miR-214 and Qki Affect Dendritic Growth in Vivo-To confirm the effects of miR-214 and Qki on dendritic growth in vivo, we introduced constructs expressing GFP alone (control) or GFP together with miR-214 or Qki into embryonic cerebral cortices by in utero electroporation at E14, and the brains were fixed at P10. Almost all of the transduced cells were situated in layer 2/3-4 (Fig.  8A). Expression of miR-214 significantly increased total dendrite length and branch number compared with control (Fig. 8, B-E).
Sholl analysis also revealed that overexpression of miR-214 promoted dendritic arborization (Fig. 8F). In addition, the total number of crossings was increased in miR-214-expressing neurons (Fig. 8G). In contrast, expression of Qki clearly suppressed dendritic formation compared with control (Fig. 8, B-E). Dendritic complexity was also decreased by Qki expression (Fig. 8, F and G). Taken together, these results suggest that the miR-214-Qki pathway regulates dendritic development in vivo.

Discussion
As dendrites are the main site of synaptic input into neurons, the structure of the dendrite branch and the targeting of dendrites into appropriate territories are critical determinants of the input properties of neurons. Therefore, the regulation of dendritic morphogenesis is crucial for the establishment of functional neuronal circuits, and dysregulation of dendrite formation may be a cause of neurological diseases such as psychiatric disorders (4, 5, 38, 39).
Recent research has revealed that miRNAs act as regulators of many aspects of neuronal development such as neuronal differentiation, neuronal outgrowth, and dendritic spine morphogenesis (11, 40 -42). Although it has recently been reported that miR-137 negatively regulates aspects of neuronal maturation, including dendritic formation (13), the role of miRNA in dendrite development remains poorly understood.
In this study, we investigated the functional role of miR-214 in primary cultured hippocampal neurons. We observed a tran-

miR-214 Regulates Dendrite Development by Targeting Qki
sient up-regulation of primary miR-214 expression at an early stage in the development of hippocampal neurons in culture, and its expression decreased at later stages. In contrast, the level of mature miR-214 gradually increased during neuronal maturation. These observations made us think that miR-214 might play a role in neuronal maturation and also suggested that the abundance of mature miR-214 is tightly controlled at the posttranscriptional level during neuronal maturation. Here, we demonstrated that overexpression of miR-214 increases total dendritic length, branch numbers, and dendritic complexity. We also showed that loss of miR-214 function inhibits dendritic arborization. These data clearly indicate that miR-214 positively controls dendritic development.
Identifying downstream mRNA targets is essential to understand the function of miRNAs. By performing database searches and functional screening, we identified Qki as a candidate target gene of miR-214. Qki governs post-transcriptional regulation of its mRNA ligands by regulating pre-mRNA splicing (43,44), mRNA turnover (45), and translation (46). Qki has also been shown to regulate cellular processes, including apoptosis, the cell cycle, and development (47,48). In particular, Qki is involved in oligodendrocyte development and myelination (49,50) in the central nervous system. However, the function of Qki in neurons has not yet been investigated. In this study, we demonstrated that overexpression and knockdown of Qki impeded and enhanced dendritic morphogenesis, respectively, suggesting that Qki negatively regulates dendritic formation. The finding that Qki abolishes dendritic phenotypes induced by the expression of miR-214 further supports the negative effects of Qki on dendritic development and its role as a downstream effector of miR-214. Although Qki clearly functions downstream of miR-214, database searches identified other predicted miR-214 targets, and we therefore cannot rule out the possibility that miR-214 can modulate the expression of these genes. Further experiments to identify additional miR-214 targets will give us more insight into the molecular function of miR-214 during neuronal development.
How does Qki regulate dendritic development? Previous work has identified many putative mRNA targets of Qki, using SELEX (systematic evolution of ligands by exponential enrichment) and bioinformatic analysis (51). Interestingly, among these candidate targets are Wnt2a and Rab5a. The Wnt-dishevelled pathway regulates dendrite morphogenesis in mammalian neurons, whereas Rab5, a component of the early endocytic pathway, promotes dendritic branching of fly dendritic arborization neurons (6). Thus, it is plausible that Qki controls dendrite development by regulating these mRNAs. In addition, because actin is one of the major structural components that underlie dendrite morphology, regulators of actin are implicated in dendrite morphogenesis. Another study showed that Qki regulates actin-interacting protein-1 (AIP1) mRNA stability during oligodendrocyte differentiation (52). Thus, it is possible that Qki also targets AIP1 in neurons, thereby regulating dendritic morphogenesis. It will be of interest to determine how Qki controls dendritic development in future studies.
Multiple studies have implicated QKI in schizophrenia (37,53). Furthermore, it is known that altered dendritic morphology contributes to various neurological disorders, including schizophrenia (54 -56). Here, we described an important function of miR-214 in dendritic growth as a regulator of Qki expression in hippocampal neurons. Thus, it is possible that impairments of dendritic development by miR-214-Qki pathway dysfunction lead to the abnormal dendritic phenotypes observed in psychiatric diseases. Given our demonstration that miR-214 targets Qki, it will be intriguing to explore further whether miR-214 is a candidate susceptibility gene for major mental illness, and whether miR-214 knock-out mice show any of behavioral abnormalities associated with psychiatric diseases.
Taken together, our findings uncover an important role for the miR-214-Qki pathway in dendritic development (Fig. 9). We anticipate that elucidating this pathway in more detail will also contribute to a deeper understanding of the molecular mechanisms underlying neuropsychiatric disorders such as schizophrenia.
Author Contributions-K. I. performed all of the experiments with support from H. N. K. T. conceived and designed the research. K. I., K. T., and K. N. wrote the manuscript. K. N. coordinated and supervised the study. All authors reviewed and approved the final version of the manuscript. pre-miR-214 is processed from pri-miR-214 (Dnm3os). pre-miR-214 is further processed into mature miR-214 -5p and -3p. miR-214-3p binds to the Qki 3ЈUTR and suppresses the expression of Qki, a protein that negatively regulates dendritic development in hippocampal neurons. Consequently, miR-214 promotes dendritic growth in hippocampal neurons.