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. 2015 Dec 25;26(2):239–253. doi: 10.1038/cr.2015.152

NudC regulates actin dynamics and ciliogenesis by stabilizing cofilin 1

Cheng Zhang 1,*, Wen Zhang 1,*, Yi Lu 1,*, Xiaoyi Yan 1,2, Xiumin Yan 3, Xueliang Zhu 3, Wei Liu 1, Yuehong Yang 1,2,*, Tianhua Zhou 1,2,*
PMCID: PMC4746604  PMID: 26704451

Abstract

Emerging data indicate that actin dynamics is associated with ciliogenesis. However, the underlying mechanism remains unclear. Here we find that nuclear distribution gene C (NudC), an Hsp90 co-chaperone, is required for actin organization and dynamics. Depletion of NudC promotes cilia elongation and increases the percentage of ciliated cells. Further results show that NudC binds to and stabilizes cofilin 1, a key regulator of actin dynamics. Knockdown of cofilin 1 also facilitates ciliogenesis. Moreover, depletion of either NudC or cofilin 1 causes similar ciliary defects in zebrafish, including curved body, pericardial edema and defective left-right asymmetry. Ectopic expression of cofilin 1 significantly reverses the phenotypes induced by NudC depletion in both cultured cells and zebrafish. Thus, our data suggest that NudC regulates actin cytoskeleton and ciliogenesis by stabilizing cofilin 1.

Keywords: NudC, actin dynamics, ciliogenesis, cofilin 1, zebrafish development

Introduction

Cilia are evolutionarily conserved microtubule-based organelles that project from the cell surface. In vertebrates, cilia are classified as motile or nonmotile (primary). Motile cilia often occur in epithelial tissues to generate fluid flow, while non-motile cilia are distributed widely and are considered critical for extracellular signal reception and transduction1,2. Cilia play essential roles in vertebrate development, including establishment of left-right asymmetry, and brain and kidney development3,4,5. Disruption of cilia structure or motility is associated with a range of human disorders termed ciliopathies, such as primary ciliary dyskinesias, cystic kidney diseases and situs inversus6,7,8,9.

Accumulating data suggest that actin dynamics affects ciliogenesis. Either silencing of actin-related protein ARP3 or treatment with actin polymerization inhibitor cytochalasin D facilitates cilia formation and promotes cilia elongation in mammalian cells10. Recently, we found that miR-129-3p, a microRNA conserved in vertebrates, promotes both ciliogenesis and the axoneme growth by repressing branched F-actin formation11. However, the regulation of ciliogenesis by actin dynamics remains elusive.

Nuclear distribution gene C (NudC) was first identified as a regulator of nuclear movement in the filamentous fungus Aspergillus nidulans12. We and other groups have found that NudC plays crucial roles in diverse cellular processes, including cell division and neuronal migration, partially by modulating the dynein complex13,14,15. A growing body of evidence implies that NudC functions as a co-chaperone of Hsp90 to stabilize client proteins16,17,18. Proteomics data from our laboratory and others indicate that NudC may interact with cofilin 117,18, a key regulator of actin dynamics, yet little is known about the role of NudC in actin cytoskeleton.

In this report, we find that NudC is essential for actin organization and dynamics by regulating the stability of cofilin 1. Depletion of either NudC or cofilin 1 facilitates ciliogenesis in mammalian cells and results in ciliary defects in zebrafish. More importantly, exogenous expression of cofilin 1 significantly reverses the phenotypes caused by NudC knockdown in either cultured cells or zebrafish. These results indicate a critical role of NudC in actin cytoskeleton and ciliogenesis by stabilizing cofilin 1.

Results

Depletion of NudC influences actin dynamics

To determine the role of NudC in actin cytoskeleton, we first examined the cellular localization of NudC together with actin in RPE-1 cells. The data revealed that NudC was mainly localized in cytoplasm and concentrated in lamellipodia (Supplementary information, Figure S1). Then, we employed lentivirus-mediated RNAi targeting two different regions of NudC mRNA in RPE-1 cells and found that the protein level of NudC was substantially reduced (Figure 1A). Immunostaining results showed that thick stress fibers were frequently detected in RPE-1 cells depleted of NudC (Figure 1B), which was reversed by ectopic expression of RNAi-resistant NudC (Supplementary information, Figure S2). Scratch wound assays further displayed that NudC depletion significantly inhibited collective cell migration and lamellipodia formation at the leading edge (Figure 1C, 1D and Supplementary information, Figure S3). Kymographs of lamellipodial protrusion confirmed that knockdown of NudC led to decreases in protrusion velocity with concomitant increases in protrusion persistence (Figure 1E-1G). Moreover, we also observed that NudC depletion resulted in impaired cell spreading (Figure 1H and 1I). These data strongly indicate that NudC is a crucial regulator of actin dynamics.

Figure 1.

Figure 1

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Depletion of NudC disrupts actin organization. RPE-1 cells were treated with lentivirus-delivered shRNAs, NudC RNAi-1 or -2, targeting different regions of NudC. (A) Western blotting showing efficient suppression of NudC. GAPDH is the loading control. (B) Immunofluorescence revealing thick stress fibers (arrows) in NudC-depleted cells. (C, D) Immunostaining showing less lamellipodia formation (arrowheads) in cells depleted of NudC at the leading edge after scratching (C). Cells with lamellipodia are counted (D). More than 50 cells are analyzed per experiment. (E-G) Kymographs revealing decreases in protrusion dynamics of NudC-depleted cells. Minimum intensity projection of a 250-frame movie (3 s per frame) is presented on the right. Pixel intensities along a one-pixel-wide line (white) are used to generate the kymograph presented on the left (E). The velocity (F) and persistence (G) of lamellipodia protrusion are calculated. (H, I) Phase contrast images showing impaired cell spreading in NudC knockdown cells. The areas of cell spreading are outlined by dashed lines and measured by Image J software (NIH). More than 20 cells are counted in each experiment. DNA is labeled with DAPI. Scale bars represent 20 μm. Quantitative data are derived from at least three independent experiments and expressed as mean ± SD. n, sample size. *P < 0.05; **P < 0.01; ***P < 0.001.

NudC suppresses primary cilia assembly

As it has been reported that actin dynamics affects ciliogenesis in mammalian cells10,11, we tested the potential role of NudC in primary cilia assembly. Given that cilia typically form during G1 or G0 phase and disassemble around the time of mitosis, serum starvation induces ciliogenesis and addition of serum inhibits ciliation6,19,20. In this study, cilia length was measured under serum deprivation and the percentage of ciliated cells was calculated under serum-rich condition. NudC depletion in RPE-1 cells caused a significant elongation of primary cilia in the absence of serum and increased the percentage of the ciliated cells in the presence of serum (Figure 2A-2F). Induction of ciliogenesis by NudC knockdown was significantly reversed by ectopic expression of RNAi-resistant NudC (Supplementary information, Figure S4). In consistence with the results above, knockdown of NudC in HEK293T cells also substantially induced primary cilia assembly (Supplementary information, Figure S5). Given that ciliation is associated with cell cycle regulation1,21,22, we determined whether NudC depletion influences cell cycle. Flow cytometry showed that there was no significant difference between the control and NudC-depleted RPE-1 cells during cell cycle progression under our conditions (Figure 2G and 2H). As inhibition of actin dynamics has been shown to induce ciliogenesis by accumulating ciliogenic membrane vesicles positive for Rab11a around the centrosome regions10,11,20, we tested whether NudC depletion promotes ciliogenesis via the similar mechanism. In NudC-depleted RPE-1 cells, Rab11a-positive vesicles were more frequently accumulated around the centrosome region compared with the control cells (Figure 2I and 2J). Furthermore, overexpression of NudC considerably inhibited ciliation in RPE-1 cells (Figure 2K-2N). Thus, these results suggest that NudC plays an inhibitory role in ciliogenesis in mammalian cells.

Figure 2.

Figure 2

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NudC suppresses ciliogenesis in mammalian cells. (A-C) RPE-1 cells treated with either NudC RNAi-1 or -2 under serum starvation are subjected to the following analyses. Immunoblotting confirms significant knockdown of NudC (A). GAPDH is the internal control. Immunofluorescence with anti-Arl13b (cilia marker) and γ-tubulin (γ-tub) antibodies reveals an increase in cilia length after NudC depletion (B). Boxed regions are enlarged in insets. Lengths of more than 120 cilia (per experiment) are measured by Image J software (C). (D-J) RPE-1 cells treated with either NudC RNAi-1 or -2 are analyzed. Western blotting shows significant suppression of NudC (D). Immunostaining reveals spontaneous ciliogenesis (arrow) in NudC knockdown cells (E). Percentage of cells with cilia in each experiment (F). Flow cytometry reveals no significant difference between control and NudC-depleted cells during cell cycle progression (G, H). Immunofluorescence with anti-acetylated tubulin (ace-tub, cilia marker) and Rab11a antibodies reveals an increase in Rab11a-positive vesicles around the centrosome regions (arrowheads) in NudC-depleted cells (I, J). More than 150 cells are scored each time. (K-N) Overexpression of NudC suppresses ciliogenesis. RPE-1 cells transfected with the indicated vectors are subjected to western blotting (K) and immunostaining (L). Lengths of more than 60 cilia (per experiment) are measured by Image J software (M). Over 180 cells with cilia are counted in each experiment (N). DNA is visualized by DAPI. Scale bars represent 10 μm. Quantitative data from at least three independent experiments are shown as mean ± SD. n, sample size. ***P < 0.001; ns, not significant (P > 0.05).

NudC knockdown results in ciliary phenotypes in zebrafish

Cilia have been demonstrated to be involved in various developmental processes in vertebrates5,11,23,24; therefore, we explored the function of NudC during zebrafish development. Zebrafish NudC shares high homology with human NudC (identity, 72.0%; similarity, 85.0%) and the polyclonal antibodies against human NudC also recognized zebrafish NudC (Figure 3A). RT-PCR analysis revealed that NudC mRNA was ubiquitously expressed in embryonic and early larval stages of zebrafish (Supplementary information, Figure S6A). Whole mount in situ hybridization showed that NudC was detected in the brain, eyes, pronephros and so on (Supplementary information, Figure S6B-S6I). We then designed antisense morpholino oligonucleotides (MOs) to block the translation of NudC mRNA (NudC MO-1) and found that injection with low dose of NudC MO-1 (2.5 ng per embryo) obviously decreased endogenous NudC in zebrafish embryos (Figure 3A). NudC morphants exhibited several ciliary defects such as curved body (56.7%), pericardial edema (87.7%) and hydrocephalus (27.1%) at 72 h post fertilization (hpf) (Figure 3B and 3C). Histological cross-sections confirmed the existence of hydrocephalus and displayed dilation of anterior pronephric duct in NudC morphants (Figure 3D and 3E). Furthermore, we tested the position of the heart tube (using cardiac myosin light chain 2, cmlc2, as a marker) and distribution of an early asymmetry-determining factor (lefty2) in NudC morphants. The results revealed that cmlc2 (34.8%) and lefty2 (43.3%) were not restricted to the left side of the embryos injected with NudC MO-1 (Figure 3F-3I), implying an essential role of NudC in controlling left-right asymmetry. Importantly, all of these defects caused by NudC MO-1 were effectively reversed by exogenous expression of NudC mRNA (Figure 3B, 3C, 3G and 3I).

Figure 3.

Figure 3

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NudC depletion induces multiple ciliary defects in zebrafish. Embryos were injected with 2.5 ng control morpholino (Ctrl MO), 2.5 ng NudC MO-1, 25 pg NudC mRNA or 2.5 ng NudC MO-1 plus 25 pg NudC mRNA and collected at the indicated times. (A) Western analysis showing efficiency of NudC knockdown. α-tubulin (α-tub) is used as the internal control. (B, C) Bright-field micrographs of embryos showing body curvature, pericardial edema (arrow) and hydrocephalus (arrowhead) in NudC morphants at 72 hpf. Scale bar, 500 μm. (D, E) Sections of brain (D) and pronephric duct (E) of NudC morphants displaying hydrocephalus (asterisk) and dilated pronephric ducts (arrows) at 72 hpf. Black dashed lines indicate the boundaries of pronephric ducts. Scale bar, 200 μm. (F-I) Whole mount in situ hybridization with cmlc2 at 30 hpf (F) or lefty2 at 22 hpf (H) shows defective left-right asymmetry (dorsal view). Scale bar, 500 μm. Percentages of different expression patterns of cmlc2 (G) or lefty2 (I) are also presented. (J, K) Immunofluorescence with anti-ace-tub antibody (green) reveals an increase in cilia length in KV of NudC morphants at 8-somite stage (8 ss). Scale bar, 10 μm. Cilia length in KV is measured using Image J software (K). (L) Immunostaining of anterior pronephric ducts shows longer cilia in NudC morphant at 24 hpf. Scale bar, 10 μm. (M, N) Images extracted from video of anterior pronephric duct showing an enlarged lumen in NudC morphant at 48 hpf. Embryos (lateral views) are oriented with anterior to the left and dorsal up (M). White dashed lines and red lines indicate the boundaries and lumens of pronephric ducts, respectively. Scale bar, 20 μm. The width of lumen is measured using Image J software (N). Data from at least three independent experiments are represented as mean ± SD. n, sample size. ***P < 0.001; ns, not significant (P > 0.05).

Given that Kupffer's vesicle (KV) is a ciliated organ that governs left-right asymmetry of zebrafish embryo25,26, we performed whole mount immunofluorescence (IF) and observed that NudC knockdown significantly increased cilia length in KV, which was reversed by ectopic expression of NudC mRNA (Figure 3J and 3K). As it has been reported that the motile cilia in pronephric ducts are crucial for fluid flow5,11,23, we examined whether NudC influences the cilia in pronephric ducts. Immunostaining showed that NudC depletion caused longer cilia in anterior pronephric ducts of NudC morphants, which was reversed by exogenous expression of NudC mRNA (Figure 3L). Video microscopy showed that the cilia in enlarged pronephric ducts of NudC morphants were randomly orientated and beat in an uncoordinated manner, which were also significantly rescued by ectopic expression of NudC mRNA (Figure 3M and 3N; Supplementary information, Movies S1-S4).

In order to minimize the off-target effects of NudC MO, we employed another MO targeting a different region of NudC mRNA (NudC MO-2), and observed similar phenotypes to that of NudC MO-1, which were also significantly reversed by NudC mRNA (Supplementary information, Figure S7). A recent study showed that generation of robust biallelic mutations by CRISPR/Cas9 system in the injected zebrafish embryos appears to allow for phenotypic analysis directly in the F0 animals27. To further confirm the function of NudC during zebrafish development, we designed a guide RNA (gRNA) to target zebrafish NudC. Phenotypes of Cas9/NudC-gRNA-injected embryos were similar to that of NudC morphants (Supplementary information, Figure S8). These data together suggest a crucial role of NudC in ciliation and cilia-mediated developmental processes in zebrafish.

NudC binds to and stabilizes cofilin 1

Mass spectrometry data of proteins co-immunoprecipitated with NudC reported by our group and others have indicated that cofilin 1 may interact with NudC17,18. The similar roles of NudC and cofilin 1 in actin dynamics prompted us to investigate the biochemical interaction between these two proteins28,29,30. GST pull-down and immunoprecipitation experiments revealed that NudC associated with cofilin 1 (Figure 4A and 4B). More importantly, endogenous NudC was also able to interact with cofilin 1 in RPE-1 cells (Figure 4C and 4D). IF combined with scratch wound assay confirmed that NudC was colocalized with cofilin 1 at the leading edge (Figure 4E). These results strongly suggest that NudC forms a complex with cofilin 1 in mammalian cells.

Figure 4.

Figure 4

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NudC binds to and stabilizes cofilin 1. (A) GST pull-down assay revealing the interaction between NudC and cofilin 1 in vitro. Input proteins are stained with Coomassie brilliant blue. 5% of total input from RPE-1 cell lysates is shown. (B-D) Co-immunoprecipitation confirms that NudC is associated with cofilin 1 in vivo. RPE-1 cells transfected with the indicated vectors (B) or not (C, D) are subjected to immunoprecipitation with indicated antibodies and western blotting. 3% of total input is shown. (E) Immunofluorescence revealing colocalization of NudC and cofilin 1. DNA is stained with DAPI (blue). Higher magnification of the boxed region is shown in inset. Scale bar, 20 μm. (F) Western analysis showing significantly decreased levels of cofilin 1 in NudC-depleted cells. Band intensities are quantified using Image J software. (G) Quantitative RT-PCR revealing that NudC RNAi has no significant effect on cofilin 1 mRNA. GAPDH is the internal control. (H) Proteasome inhibitor MG132 reverses cofilin 1 degradation induced by NudC depletion. RPE-1 cells treated with or without NudC RNAi were incubated with either 5 μM MG132 or DMSO (vehicle), and subjected to western blotting. (I) NudC depletion induces the ubiquitination of cofilin 1. RPE-1 cells depleted of NudC or not were transfected with the indicated vectors and treated with 5 μM MG132. Immunoprecipitates with anti-Flag antibody from cell lysates are analyzed by immunoblotting. 3% of total input is shown Quantitative data from three independent experiments are shown as mean ± SD. n, sample size. **P < 0.01; ***P < 0.001; ns, not significant (P > 0.05).

Previous data from our laboratory and others suggest that NudC may be involved in the regulation of protein stability17,18. We tested whether NudC regulates the stability of cofilin 1 and found that NudC depletion substantially decreased the protein level of cofilin 1, but not its mRNA level (Figure 4F and 4G). Ubiquitin proteasome pathway is responsible for the targeted degradation of intracellular proteins such as cofilin 131,32; we thus investigated whether the proteasome pathway is involved in the regulation of cofilin 1 stability by NudC. Indeed, degradation of cofilin 1 after NudC depletion was blocked by MG132, a proteasome inhibitor (Figure 4H), and NudC depletion significantly increased the ubiquitination of cofilin 1 (Figure 4I). Thus, NudC depletion may induce the degradation of cofilin 1 via the ubiquitin proteasome pathway.

NudC acts upstream of cofilin 1 to regulate cilia assembly

Based on the data that NudC influences ciliogenesis and cofilin 1 stability (Figures 2, 3, 4), we assumed that NudC may modulate ciliogenesis by regulating cofilin 1 stability. Depletion of cofilin 1 by two different small interfering RNAs (siRNAs) in RPE-1 cells caused a significant elongation of primary cilia in the absence of serum and increased the percentage of the ciliated cells in the presence of serum (Figure 5A-5F). Consistent with the data above, knockdown of cofilin 1 in HEK293T cells also considerably promoted cilia assembly (Supplementary information, Figure S9). More Rab11a-positive vesicles were observed around the centrosome regions in cofilin 1-depleted cells compared with the control (Figure 5H and 5G). Furthermore, overexpression of cofilin 1 effectively inhibited ciliogenesis (Figure 5I-5L). These results indicate that cofilin 1 plays a similar role in ciliogenesis as NudC.

Figure 5.

Figure 5

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Cofilin 1 suppresses cilia assembly in mammalian cells. (A-C) RPE-1 cells were transfected with siRNA oligos, cofilin 1 RNAi-1 or -2, targeting different regions of cofilin 1 mRNA. Western blotting shows efficient knockdown of cofilin 1 (A). GAPDH is the internal control. Immunofluorescence with anti-Arl13b and γ-tubulin (γ-tub) antibodies reveals an increase in cilia length after cofilin 1 depletion (B). Insets are higher magnifications of the boxed areas. Cilia length (more than 70 cilia in each experiment) is scored using Image J software (C). (D-H) RPE-1 cells were treated with cofilin 1 RNAi. Western blotting confirms significant depletion of cofilin 1 (D). Immunostaining with antibodies reveals spontaneous ciliogenesis (arrows) in cofilin 1 knockdown cells (E). Percentage of cells with cilia in each treatment (F). Immunofluorescence reveals Rab11a-positive vesicles are frequently accumulated around the centrosome regions (arrowheads) in cofilin 1-depleted cells (G, H). More than 150 cells are scored each time. (I-L) Overexpression of cofilin 1 suppresses ciliogenesis. Western blotting (I) and immunostaining (J) of RPE-1 cells transfected with the indicated vectors. Insets show higher magnifications of cilia. Cilia length (more than 40 cilia in each experiment) is measured using Image J software (K). Percentage of cells with cilia in each treatment (L). DNA is labeled with DAPI. Scale bars represent 10 μm. Quantitative data from at least three independent experiments are shown as mean ± SD. n, sample size. ***P < 0.001.

To determine whether NudC regulates ciliogenesis via modulating cofilin 1 expression, we performed RNAi rescue assays in mammalian cells. Exogenous expression of cofilin 1 significantly reversed the abnormal ciliogenesis induced by NudC depletion, but not vice versa (Figure 6A-6D and 6G-6J). Furthermore, double knockdown of NudC and cofilin 1 did not show synergistic effects on ciliogenesis compared with that of cofilin 1 depletion (Figure 6E, 6F, 6K and 6L), suggesting that NudC and cofilin 1 may act in the same pathway to modulate ciliogenesis.

Figure 6.

Figure 6

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Cofilin 1 rescues the ciliary defects induced by NudC depletion, but not vice versa. (A-F) RPE-1 cells treated with the indicated RNAi and expression vectors and subjected to serum starvation are analyzed by western blotting and immunofluorescence. Cilia length is determined by Image J software. Ectopic expression of cofilin 1 reverses abnormal cilia elongation caused by NudC depletion (A, B). Exogenous expression of NudC fails to inhibit aberrant cilia elongation induced by cofilin 1 knockdown (C, D). Double depletion of NudC and cofilin 1 has no synergistic effect on cilia length (E, F). (G-L) RPE-1 cells treated with the indicated RNAi and expression vectors are analyzed by immunoblotting and immunostaining. Percentages of cells with cilia in different treatments are shown. Ectopic expression of cofilin 1 inhibits spontaneous ciliogenesis caused by NudC knockdown (G, H). Exogenous expression of NudC is unable to reverse spontaneous ciliogenesis induced by cofilin 1 depletion (I, J). NudC knockdown shows no synergistic effect with cofilin 1 depletion on ciliation (K, L). Quantitative data derived from at least three independent experiments are shown as mean ± SD. n, sample size. ***P < 0.001; ns, not significant (P > 0.05).

Cofilin 1 rescues the ciliary phenotypes in NudC morphants

To further investigate the role of cofilin 1 in ciliogenesis during zebrafish development, we used MO to deplete cofilin 1 and found that injection with low dose of cofilin 1 MO-1 (2.0 ng per embryo) effectively decreased endogenous cofilin 1 in embryos (Supplementary information, Figure S10A). Cofilin 1 morphants displayed several ciliary defects, including curved body (42.0%) and pericardial edema (81.9%; Figure 7A and 7B), which were significantly reversed by exogenous expression of cofilin 1 mRNA (Supplementary information, Figure S10). Whole mount in situ hybridization revealed that cmlc2 was not restricted to the left side in 48.4% of embryos injected with cofilin 1 MO-1, and lefty2 was not restricted to the left side in 46.3% of cofilin 1 morphants (Figure 7C-7F). Immunostaining of cofilin 1 morphants showed a significant increase of cilia length in KV compared with the control (Figure 7G and 7H). To rule out the off-target effects of MO, we employed another MO targeting a different region of cofilin 1 mRNA (cofilin 1 MO-2), and observed similar phenotypes (Supplementary information, Figure S11). Furthermore, the phenotypes of Cas9/cofilin 1-gRNA-injected embryos were consistent with those of cofilin 1 morphants (Supplementary information, Figure S12). It is important to point out the similarities between the phenotypes caused by cofilin 1 depletion and NudC knockdown.

Figure 7.

Figure 7

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Cofilin 1 reverses the ciliary defects in NudC morphants. Embryos were injected with Ctrl MO (2.5 ng), NudC MO (2.5 ng), cofilin 1 MO (2.0 ng) or NudC MO (2.5 ng) plus cofilin 1 mRNA (25 pg) and collected at the indicated times. (A, B) Bright-field micrographs showing body curvature and pericardial edema (arrow) in cofilin 1 morphant at 72 hpf. Ectopic expression of cofilin 1 mRNA rescues the ciliary phenotypes induced by NudC depletion. Scale bar, 500 μm. (C-F) Whole mount in situ hybridization with cmlc2 at 30 hpf (C) or lefty2 at 22 hpf (E) reveals that the defective left-right asymmetry in NudC morphants is reversed by cofilin 1 mRNA (dorsal view). Scale bar, 500 μm. Percentages of different expression patterns of cmlc2 (D) and lefty2 (F) are also shown. (G, H) Immunofluorescence with anti-ace-tub antibody (green) at 8 ss shows that cofilin 1 mRNA rescues abnormal cilia elongation in NudC morphants. Scale bar, 10 μm. Cilia length in KV is measured by Image J software. The data are presented as mean ± SD derived from at least three independent experiments. n, sample size. *P < 0.05; ***P < 0.001; ns, not significant (P > 0.05). (I) Working model for the role of NudC in actin cytoskeleton and ciliogenesis. NudC binds to and stabilizes cofilin 1 to regulate actin dynamics and ciliogenesis. Depletion of NudC causes cofilin 1 degradation and inhibits actin dynamics possibly via the ubiquitin-proteasome pathway, resulting in accumulation of ciliogenic vesicles at basal body to facilitate cilia assembly.

Furthermore, ectopic expression of cofilin 1 partially, but significantly, reversed the ciliary phenotypes induced by NudC depletion with either NudC MO-1 or MO-2 (Figure 7A-7H, Supplementary information, Figures S11-S13 and Movies S5-S8), suggesting that NudC may regulate ciliation and cilia-mediated developmental events by modulating cofilin 1 expression in zebrafish.

Discussion

In this study, we provide evidence that NudC plays essential roles in regulating actin cytoskeleton, ciliogenesis and zebrafish development by stabilizing cofilin 1. Actin cytoskeleton participates in many cellular processes, including muscle contraction, cell motility and cell signaling. Cofilin 1 has a pivotal role in actin dynamics by modulating actin polymerization and depolymerization through its severing activity33,34,35. Here we find that depletion of NudC causes an accumulation of bundled stress fibers and inhibits cell spreading and lamellipodia formation (Figure 1), resembling the cellular phenotypes induced by cofilin 1 knockdown29,30,33. Furthermore, our results show that NudC forms a complex with cofilin 1, colocalizes with cofilin 1 especially at the leading edge and influences the stability of cofilin 1 (Figure 4). Thus, these data suggest that NudC may act as an upstream regulator of actin cytoskeleton and dynamics by stabilizing cofilin 1.

Recent data from our group and others have indicated that actin cytoskeleton is involved in ciliogenesis10,11,36,37. However, whether and how NudC regulates ciliogenesis remains unknown. In this report, we show that NudC depletion increases cilia length and facilitates spontaneous ciliation in mammalian cells (Figure 2). The ciliary phenotypes induced by NudC knockdown are similar to those by actin cytoskeleton disruption or cofilin 1 depletion10,11 (Figure 5). More importantly, depletion of either NudC or cofilin 1 causes similar ciliary defects in zebrafish, including body curvature, pericardial edema and defective left-right asymmetry (Figures 3 and 7 and Supplementary information, Figures S7, S10 and S11). Ectopic expression of cofilin 1 significantly reverses these phenotypes induced by NudC depletion in both cultured cells and zebrafish (Figures 6 and 7). Taken together, these findings support the hypothesis that NudC may regulate ciliogenesis via cofilin 1-mediated actin dynamics (Figure 7I).

Previous results showed that NudC is highly expressed in ciliated epithelia and localized in motile cilia38. Interestingly, when we examined the localization of NudC together with cilia in RPE-1 cells, we found that NudC mainly distributed in the cytoplasm, but not in cilia under our conditions (Supplementary information, Figure S14). This discrepancy suggests that NudC may have different expression patterns in different cells or tissues. The localization of NudC in motile cilia implies that NudC may have additional roles in the regulation of cilia.

As the studies from our laboratory and others indicate that NudC functions as a co-chaperone of Hsp90 to stabilize client proteins16,17,18, we also investigated whether NudC regulates the stability of cofilin 1 via the Hsp90 pathway. Inhibition of Hsp90 activity by geldanamycin significantly suppressed cilia assembly (Supplementary information, Figure S15), which is consistent with the previous study39. Unexpectedly, geldanamycin treatment had no significant effect on the protein level of cofilin 1 (Supplementary information, Figure S16), implying that NudC may stabilize cofilin 1 via an Hsp90-independent pathway. It will be of great interest to elucidate the detailed mechanism by which NudC influences the stability of cofilin 1.

Although depletion of either NudC or cofilin 1 in zebrafish induced the similar ciliary defects such as body curvature, pericardial edema and defective left-right asymmetry, cofilin 1 morphants did not exhibit hydrocephalus and kidney cysts that were observed in NudC morphants (Figures 3 and 7). Proteomics data from our group and others have shown that NudC may influence dozens of client proteins besides cofilin 116,17,18, indicating that there may be cofilin 1-independent pathways involved in the role of NudC in zebrafish development. Further study is clearly needed to explore the physiological significance of NudC in vertebrates.

Materials and Methods

Plasmids and oligonucleotides

GST-NudC, GFP-NudC, Flag-cofilin 1 and Myc-NudC-R vectors were constructed as described previously17,40. HA-ubiquitin and pCS107 vectors were kindly provided by Dr Ping Wang (East China Normal University) and Dr Xiao Huang (Zhejiang University), respectively. pGLV3/H1/GFP lentiviral vectors were purchased from GenePharma. To generate lentivirus expressing shRNA targeting human NudC, the following sequences were used: 5′-GAAGGGATGGCAGAGAAGC-3′ (NudC RNAi-1) and 5′-AACACCTTCTTCAGCTTCCTT-3′ (NudC RNAi-2). Oligos corresponding to the following sequences were synthesized by GenePharma: 5′-GGATCAAGCATGAATTGCAAGCAAA-3′ for cofilin 1 RNAi-141 and 5′-CATG GAAGCAGGACCAGTA-3′ for cofilin 1 RNAi-242. Full-length zebrafish NudC and cofilin 1 were amplified by RT-PCR from 72 hpf zebrafish larvae and subcloned into pCS107 vector. PCR was also used to construct RNAi-resistant NudC vectors by silent mutation of five nucleic acids in the RNAi targeting region of NudC mRNA. NudC MO-1 (5′-TCTTTCGTCATCGTCACCCATTTTC-3′) targeted part of the open reading frame of zebrafish NudC mRNA, the rescue construct was engineered to change the nucleotide sequence without altering the encoded protein. As NudC MO-2, cofilin 1 MO-1 and MO-2 separately target the 5′- UTR sequence of NudC and cofilin 1 mRNA, the open reading frames of these two genes were simply cloned into pCS107 vector for rescue experiments43. Capped and polyadenylated RNAs were synthesized with the SP6 mMessage mMachine kit (Ambion). All of these constructs were confirmed by DNA sequencing.

Cell culture and transfection

RPE-1 cells were maintained in DMEM/F12 (Corning) containing 10% serum (PAA Laboratories) at 37 °C in 5% CO2. HEK293T cells were cultured in DMEM (Corning) with 10% serum at 37 °C in 5% CO2. To examine cilia length, culture medium was replaced with serum-free medium when cells were 90% confluent, then cultured for 48 h before use. The plasmids and synthetic oligonucleotides were transfected using Lipofectamine 2000 (Invitrogen) according to the manufacturer's instructions.

Antibodies

For IF and western blotting (WB), mouse monoclonal antibodies against acetylated tubulin (Sigma, 1:1 000 for IF), c-Myc (Santa Cruz, 1:1 000 for WB, 1:200 for IF), γ-tubulin (Sigma, 1:1 000 for IF), α-tubulin (Sigma, 1:5 000 for WB), GAPDH (Proteintech, 1:10 000 for WB) and cofilin 1 (Proteintech, 1:1 000 for WB, 1:200 for IF) were used. Rabbit polyclonal antibodies against ARL13b (Proteintech, 1:200 for IF), CETN1 (Proteintech, 1:200 for IF) and Rab11a (Invitrogen, 1:200 for IF) were also employed. Anti-NudC antibody was generated using bacterially expressed GST-NudC as an antigen and subjected to affinity purification (Proteintech, 1:500 for WB, 1:50 for IF). Secondary antibodies for IF analyses were Alexa Fluor 488-, 568- and 647-conjugated anti-rabbit or anti-mouse IgG (Invitrogen, 1:500). Goat anti-mouse or anti-rabbit secondary antibodies (LI-COR, 1:5 000) conjugated with either Alexa Fluor 680 or IRDye 800 were used for WB.

Kymography analysis

For kymography, phase-contrast time-lapse sequences were captured using a ×40 oil objective on an Olympus IX81-FV1000 confocal microscope. Images were recorded for 10-15 min at a rate of one frame per 3 s. Kymographs were produced and analyzed by Image J software (NIH). Quantitative analysis of kymographs was performed as previously described44.

Scratch wound experiment

Scratch wound assays were performed as described previously45. In brief, RPE-1 cells were plated onto fibronectin (10 mg/ml)-coated coverslips and incubated at 37 °C in 5% CO2 to create a confluent monolayer. The monolayer was scratched using a sterile pipette tip. The cells were washed to remove the debris and then replaced with fresh medium. For lamellipodia formation assay or colocalization assay, the cells were fixed and stained after 3 h of scratching.

Cell spreading assay

Cell spreading assays were performed as described previously32. In brief, cells were resuspended in serum-free media after trypsinization and incubated at 37 °C in 5% CO2 for 1 h. Cells were collected and reseeded on fibronectin (10 mg/ml)-coated plates. After 1 h, cells were fixed with 4% paraformaldehyde and photographed in random fields.

Flow cytometry

For flow cytometry analysis, cells were collected, washed once with cold phosphate-buffered saline and then fixed in 70% ethanol. DNA was stained with propidium iodide (Sigma) for 30 min at 37 °C. The samples were analyzed using a FC 500 MCL Flow Cytometer (Beckman Coulter).

GST pull-down assay

GST pull-down assays were performed as described previously15. To detect the association between NudC and cofilin 1, blots were probed with antibodies indicated in the text.

Immunoprecipitation and western blotting

Immunoprecipitation was performed as previously described46,47. In brief, cells transfected with the indicated vectors were subjected to immunoprecipitation with anti-Flag antibody-coupled beads (Sigma). Endogenous NudC and cofilin 1 were immunoprecipitated with anti-cofilin 1 and NudC antibodies, respectively. Protein samples were separated by SDS-PAGE gel, transferred to polyvinylidene fluoride membrane (Millipore), incubated with indicated antibodies and detected by an enhanced chemiluminescence system (Amersham) or LI-COR Odyssey (LI-COR).

Immunofluorescence staining

Cells were grown on coverslips and fixed for 15 min with 4% paraformaldehyde. To label cilia with acetylated tubulin, cells were kept on ice for 30 min before fixation. Rhodamine phalloidin (1:500, Invitrogen) and 4,6-diamidino-2-phenylindole (Sigma) were used to visualize F-actin and DNA, respectively. The images were acquired using a ×60 oil immersion objective (Olympus IX81-FV1000). The whole mount immunostaining of zebrafish embryos was performed as previously described48. The embryos mounted in 1% low melting agarose were imaged using a 60× water immersion objective (Olympus BX61W1-FV1000).

Quantitative real-Time RT-PCR

Quantitative RT-PCR analyses for NudC and cofilin 1 were performed using a Bio-Rad CFX-Touch System with PrimeScript RT reagent Kit (Takara, RR037A). All of the reactions were performed in triplicate. GAPDH served as internal control.

Zebrafish maintenance and embryo production

Wild-type zebrafish (strain AB) were maintained at 28.5 °C using standard protocols. Zebrafish embryos were staged according to Kimmel et al.49.

Morpholinos and microinjection

NudC MO-1 (5′-TCTTTCGTCATCGTCACCCATTTTC-3′), NudC MO-2 (5′-TTTGACGGGTGATGCTAAGAATCAC-3′), cofilin 1 MO-1 (5′-CATGGCTGTGTCTCTGTGCTAGTCG-3′) and cofilin 1 MO-2 (5′-TCTGGGTTGGAATTGAATGAGCTGT-3′) were designed to target the translation of NudC and cofilin 1 mRNA, respectively50. MOs were synthesized by Gene Tools and injected into zebrafish embryos at 1- to 4-cell stages at the concentration described in the text. For the rescue experiments, synthetic capped mRNAs (25 pg per embryo) were co-injected into the zebrafish embryos with MOs.

In situ hybridization

Whole mount in situ hybridization was performed as described previously51. In brief, zebrafish embryos and larvae were fixed with 4% paraformaldehyde at 4 °C overnight, hybridized at 68 °C with cmlc2 or lefty2 RNA probe labeled by DIG RNA labeling kit and then stained with BM purple (Roche).

Histology

Zebrafish larvae were fixed at 72 hpf in 4% paraformaldehyde at room temperature for 2-3 h, dehydrated with ethanol, progressively infiltrated and embedded in paraffin. Sections (4 μm) were then stained with hematoxylin and eosin.

High-speed videomicroscopy

Zebrafish larvae (48 hpf) were placed in egg water containing 40 mmol/l 2,3-butanedione monoxime (Sigma) to stop the heartbeat and circulation, embedded in a low melting point agarose on a glass slide, and overlaid with a drop of egg water containing 20 mmol/l 2,3-butanedione monoxime. The images were captured using a ×60 oil immersion objective on an Olympus IX71 microscope equipped with a high-speed ANDOR Neo sCMOS digital video camera (Photron) at 250 frames per second for 2 s.

Statistics

Data are representative of at least three independent experiments. Means and SDs were calculated and are shown in the graphs. The indicated P values were obtained with one-way ANOVA using GraphPad Prism (GraphPad Software).

Author Contributions

CZ, WZ and YL designed the experiments. CZ and YL performed the experiments on cell biology. WZ performed zebrafish experiments. TZ conceived and directed the project. CZ, WZ, YL, YY, XZ, XY, WL and TZ analyzed data and wrote the manuscript.

Competing Financial Interests

The authors declare no competing financial interests.

Acknowledgments

We thank Ping Wang for providing us the HA-ubiquitin expression vector; Xiao Huang for pCS107 vector. We are grateful to Yibin Kang, Lynn W Enquist and Lu Zhao for helpful suggestions; Lei Zhu, Yirong Zhang, Biao Zhu and Yijun Liu for technical assistance. We thank State Key Laboratory of Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences and Chinese Academy of Sciences for instrument support. This work was supported by Ministry of Science and Technology of China (2012CB945004, 2013CB945603 and 2011CBA01001), National Natural Science Foundation of China (31125017, 31190063, 31100975, 31571446 and 31471259), Ministry of Education of China (20110101110103), Natural Scientific Foundation of Zhejiang Province, China (LY14C070001 and LY14C070002), the 111 Project (B13026), Department of Science and Technology of Zhejiang Province (2012C37089 and 2013TD13) and Zhejiang Provincial Program for the Cultivation of High-level Innovative Health talents.

Footnotes

(Supplementary information is linked to the online version of the paper on the Cell Research website.)

Supplementary Material

Supplementary information, Figure S1

The cellular localization of NudC together with actin in RPE-1 cells.

Click here for additional data file. (249.8KB, pdf)
Supplementary information, Figure S2

Ectopic expression of NudC rescues the actin defects induced by NudC depletion.

Click here for additional data file. (422.2KB, pdf)
Supplementary information, Figure S3

Knockdown of NudC impairs collective cell migration.

Click here for additional data file. (1MB, pdf)
Supplementary information, Figure S4

Exogenous expression of NudC rescues the ciliary defects induced by NudC depletion.

Click here for additional data file. (252.4KB, pdf)
Supplementary information, Figure S5

NudC suppresses ciliogenesis in HEK293T cells.

Click here for additional data file. (487.7KB, pdf)
Supplementary information, Figure S6

NudC expression patterns during zebrafish development.

Click here for additional data file. (1.1MB, pdf)
Supplementary information, Figure S7

Zebrafish embryos injected with NudC MO-2 exhibit multiple ciliary defects.

Click here for additional data file. (1.2MB, pdf)
Supplementary information, Figure S8

Disruption of NudC by CRISPR/Cas9 causes ciliary defects.

Click here for additional data file. (561.5KB, pdf)
Supplementary information, Figure S9

Cofilin 1 inhibits cilia assembly in HEK293T cells.

Click here for additional data file. (396.8KB, pdf)
Supplementary information, Figure S10

Exogenous expression of cofilin 1 mRNA rescues the ciliary defects in cofilin 1 morphants.

Click here for additional data file. (978.6KB, pdf)
Supplementary information, Figure S11

Cofilin 1 reverses the ciliary defects in zebrafish injected with NudC MO-2.

Click here for additional data file. (792.8KB, pdf)
Supplementary information, Figure S12

Disruption of cofilin 1 by CRISPR/Cas9 induces ciliary phenotypes.

Click here for additional data file. (558.3KB, pdf)
Supplementary information, Figure S13

Cofilin 1 partially rescues the enlarged pronephric duct in NudC morphants.

Click here for additional data file. (537.5KB, pdf)
Supplementary information, Figure S14

The cellular localization of NudC in RPE-1 cells.

Click here for additional data file. (461.6KB, pdf)
Supplementary information, Figure S15

Inhibition of Hsp90 activity suppresses ciliogenesis in mammalian cells.

Click here for additional data file. (315.8KB, pdf)
Supplementary information, Figure S16

Inhibition of Hsp90 activity has no significant effect on the protein level of cofilin 1.

Click here for additional data file. (182.9KB, pdf)
Supplementary information, Movie S1

Ciliary motility in pronephric duct of control morphant. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S2

Ciliary motility in pronephric duct of NudC morphant. Blue arrows indicate pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S3

Ciliary motility in pronephric duct of the embryo injected with NudC mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S4

Ciliary motility in pronephric duct of NudC morphant co-injected with NudC mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S5

Ciliary motility in pronephric duct of control morphant. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S6

Ciliary motility in pronephric duct of NudC morphant. Blue arrows indicate pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S7

Ciliary motility in pronephric duct of the embryo injected with cofilin 1 mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S8

Ciliary motility in pronephric duct of NudC morphant co-injected with cofilin 1 mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)

References

  1. 1Nigg EA, Raff JW. Centrioles, centrosomes, and cilia in health and disease. Cell 2009; 139:663–678. [DOI] [PubMed] [Google Scholar]
  2. 2Kim S, Dynlacht BD. Assembling a primary cilium. Curr Opin Cell Biol 2013; 25:506–511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 3Panizzi JR, Becker-Heck A, Castleman VH, et al. CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms. Nat Genet 2012; 44:714–719. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 4Stooke-Vaughan GA, Huang P, Hammond KL, Schier AF, Whitfield TT. The role of hair cells, cilia and ciliary motility in otolith formation in the zebrafish otic vesicle. Development 2012; 139:1777–1787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 5Zhao L, Yuan S, Cao Y, et al. Reptin/Ruvbl2 is a Lrrc6/Seahorse interactor essential for cilia motility. Proc Natl Acad Sci USA 2013; 110:12697–12702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. 6Fliegauf M, Benzing T, Omran H. When cilia go bad: cilia defects and ciliopathies. Nat Rev Mol Cell Biol 2007; 8:880–893. [DOI] [PubMed] [Google Scholar]
  7. 7Goetz SC, Anderson KV. The primary cilium: a signalling centre during vertebrate development. Nat Rev Genet 2010; 11:331–344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. 8Nigg EA, Cajanek L, Arquint C. The centrosome duplication cycle in health and disease. FEBS Lett 2014; 588:2366–2372. [DOI] [PubMed] [Google Scholar]
  9. 9Li Y, Ling K, Hu J. The emerging role of Arf/Arl small GTPases in cilia and ciliopathies. J Cell Biochem 2012; 113:2201–2207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. 10Kim J, Lee JE, Heynen-Genel S, et al. Functional genomic screen for modulators of ciliogenesis and cilium length. Nature 2010; 464:1048–1051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. 11Cao J, Shen Y, Zhu L, et al. miR-129-3p controls cilia assembly by regulating CP110 and actin dynamics. Nat Cell Biol 2012; 14:697–706. [DOI] [PubMed] [Google Scholar]
  12. 12Xiang X, Fischer R. Nuclear migration and positioning in filamentous fungi. Fungal Genet Biol 2004; 41:411–419. [DOI] [PubMed] [Google Scholar]
  13. 13Willins DA, Xiang X, Morris NR. An alpha tubulin mutation suppresses nuclear migration mutations in Aspergillus nidulans. Genetics 1995; 141:1287–1298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. 14Aumais JP, Williams SN, Luo W, et al. Role for NudC, a dynein-associated nuclear movement protein, in mitosis and cytokinesis. J Cell Sci 2003; 116:1991–2003. [DOI] [PubMed] [Google Scholar]
  15. 15Zhou T, Aumais JP, Liu X, Yu-Lee LY, Erikson RL. A role for Plk1 phosphorylation of NudC in cytokinesis. Dev Cell 2003; 5:127–138. [DOI] [PubMed] [Google Scholar]
  16. 16Zheng M, Cierpicki T, Burdette AJ, et al. Structural features and chaperone activity of the NudC protein family. J Mol Biol 2011; 409:722–741. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. 17Zhu XJ, Liu X, Jin Q, Cai Y, Yang Y, Zhou T. The L279P mutation of nuclear distribution gene C (NudC) influences its chaperone activity and lissencephaly protein 1 (LIS1) stability. J Biol Chem 2010; 285:29903–29910. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. 18Taipale M, Tucker G, Peng J, et al. A quantitative chaperone interaction network reveals the architecture of cellular protein homeostasis pathways. Cell 2014; 158:434–448. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. 19Spalluto C, Wilson DI, Hearn T. Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1. Febs Open Bio 2013; 3:334–340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. 20Yan X, Zhu X. Branched F-actin as a negative regulator of cilia formation. Exp Cell Res 2013; 319:147–151. [DOI] [PubMed] [Google Scholar]
  21. 21Seeley ES, Nachury MV. The perennial organelle: assembly and disassembly of the primary cilium. J Cell Sci 2010; 123:511–518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. 22Ishikawa H, Marshall WF. Ciliogenesis: building the cell's antenna. Nat Rev Mol Cell Biol 2011; 12:222–234. [DOI] [PubMed] [Google Scholar]
  23. 23Kishimoto N, Cao Y, Park A, Sun Z. Cystic kidney gene seahorse regulates cilia-mediated processes and Wnt pathways. Dev Cell 2008; 14:954–961. [DOI] [PubMed] [Google Scholar]
  24. 24Juric-Sekhar G, Adkins J, Doherty D, Hevner RF. Joubert syndrome: brain and spinal cord malformations in genotyped cases and implications for neurodevelopmental functions of primary cilia. Acta Neuropathol 2012; 123:695–709. [DOI] [PubMed] [Google Scholar]
  25. 25Essner JJ, Amack JD, Nyholm MK, Harris EB, Yost HJ. Kupffer's vesicle is a ciliated organ of asymmetry in the zebrafish embryo that initiates left-right development of the brain, heart and gut. Development 2005; 132:1247–1260. [DOI] [PubMed] [Google Scholar]
  26. 26Burdine RD, Caspary T. Left-right asymmetry: lessons from Cancun. Development 2013; 140:4465–4470. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. 27Chang NN, Sun CH, Gao L, et al. Genome editing with RNA-guided Cas9 nuclease in Zebrafish embryos. Cell Res 2013; 23:465–472. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. 28Chan AY, Bailly M, Zebda N, Segall JE, Condeelis JS. Role of cofilin in epidermal growth factor-stimulated actin polymerization and lamellipod protrusion. J Cell Biol 2000; 148:531–542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. 29Hotulainen P, Paunola E, Vartiainen MK, Lappalainen P. Actin-depolymerizing factor and cofilin-1 play overlapping roles in promoting rapid F-actin depolymerization in mammalian nonmuscle cells. Mol Biol Cell 2005; 16:649–664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. 30Wiggan O, Shaw AE, DeLuca JG, Bamburg JR. ADF/cofilin regulates actomyosin assembly through competitive inhibition of myosin II binding to F-actin. Dev Cell 2012; 22:530–543. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. 31Goldberg AL. Protein degradation and protection against misfolded or damaged proteins. Nature 2003; 426:895–899. [DOI] [PubMed] [Google Scholar]
  32. 32Yoo Y, Ho HJ, Wang C, Guan JL. Tyrosine phosphorylation of cofilin at Y68 by v-Src leads to its degradation through ubiquitin-proteasome pathway. Oncogene 2010; 29:263–272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. 33Wang W, Eddy R, Condeelis J. The cofilin pathway in breast cancer invasion and metastasis. Nat Rev Cancer 2007; 7:429–440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. 34Bravo-Cordero JJ, Magalhaes MA, Eddy RJ, Hodgson L, Condeelis J. Functions of cofilin in cell locomotion and invasion. Nat Rev Mol Cell Biol 2013; 14:405–415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. 35Bernstein BW, Bamburg JR. ADF/cofilin: a functional node in cell biology. Trends Cell Biol 2010; 20:187–195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. 36Chhabra ES, Higgs HN. The many faces of actin: matching assembly factors with cellular structures. Nat Cell Biol 2007; 9:1110–1121. [DOI] [PubMed] [Google Scholar]
  37. 37Goley ED, Welch MD. The ARP2/3 complex: an actin nucleator comes of age. Nat Rev Mol Cell Biol 2006; 7:713–726. [DOI] [PubMed] [Google Scholar]
  38. 38Gocke CD, Osmani SA, Miller BA. The human homologue of the Aspergillus nuclear migration gene nudC is preferentially expressed in dividing cells and ciliated epithelia. Histochem Cell Biol 2000; 114:293–301. [DOI] [PubMed] [Google Scholar]
  39. 39Prodromou NV, Thompson CL, Osborn DP, et al. Heat shock induces rapid resorption of primary cilia. J Cell Sci 2012; 125:4297–4305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. 40Shen M, Cai Y, Yang Y, Yan X, Liu X, Zhou T. Centrosomal protein FOR20 is essential for S-phase progression by recruiting Plk1 to centrosomes. Cell Res 2013; 23:1284–1295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. 41von Blume J, Duran JM, Forlanelli E, et al. Actin remodeling by ADF/cofilin is required for cargo sorting at the trans-Golgi network. J Cell Biol 2009; 187:1055–1069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. 42Klamt F, Zdanov S, Levine RL, et al. Oxidant-induced apoptosis is mediated by oxidation of the actin-regulatory protein cofilin. Nat Cell Biol 2009; 11:1241–1246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. 43Bill BR, Petzold AM, Clark KJ, Schimmenti LA, Ekker SC. A primer for morpholino use in zebrafish. Zebrafish 2009; 6:69–77. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. 44Bear JE, Svitkina TM, Krause M, et al. Antagonism between Ena/VASP proteins and actin filament capping regulates fibroblast motility. Cell 2002; 109:509–521. [DOI] [PubMed] [Google Scholar]
  45. 45Liang CC, Park AY, Guan JL. In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro. Nat Protoc 2007; 2:329–333. [DOI] [PubMed] [Google Scholar]
  46. 46Yang Y, Yan X, Cai Y, Lu Y, Si J, Zhou T. NudC-like protein 2 regulates the LIS1/dynein pathway by stabilizing LIS1 with Hsp90. Proc Natl Acad Sci USA 2010; 107:3499–3504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. 47Yang YF, Ran J, Liu M, et al. CYLD mediates ciliogenesis in multiple organs by deubiquitinating Cep70 and inactivating HDAC6. Cell Res 2014; 24:1342–1353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. 48Wloga D, Webster DM, Rogowski K, et al. TTLL3 is a tubulin glycine ligase that regulates the assembly of cilia. Dev Cell 2009; 16:867–876. [DOI] [PubMed] [Google Scholar]
  49. 49Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF. Stages of embryonic development of the zebrafish. Dev Dyn 1995; 203:253–310. [DOI] [PubMed] [Google Scholar]
  50. 50Lin CW, Yen ST, Chang HT, et al. Loss of cofilin 1 disturbs actin dynamics, adhesion between enveloping and deep cell layers and cell movements during gastrulation in zebrafish. PLoS One 2010; 5:e15331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. 51Oxtoby E, Jowett T. Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development. Nucleic Acids Res 1993; 21:1087–1095. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary information, Figure S1

The cellular localization of NudC together with actin in RPE-1 cells.

Click here for additional data file. (249.8KB, pdf)
Supplementary information, Figure S2

Ectopic expression of NudC rescues the actin defects induced by NudC depletion.

Click here for additional data file. (422.2KB, pdf)
Supplementary information, Figure S3

Knockdown of NudC impairs collective cell migration.

Click here for additional data file. (1MB, pdf)
Supplementary information, Figure S4

Exogenous expression of NudC rescues the ciliary defects induced by NudC depletion.

Click here for additional data file. (252.4KB, pdf)
Supplementary information, Figure S5

NudC suppresses ciliogenesis in HEK293T cells.

Click here for additional data file. (487.7KB, pdf)
Supplementary information, Figure S6

NudC expression patterns during zebrafish development.

Click here for additional data file. (1.1MB, pdf)
Supplementary information, Figure S7

Zebrafish embryos injected with NudC MO-2 exhibit multiple ciliary defects.

Click here for additional data file. (1.2MB, pdf)
Supplementary information, Figure S8

Disruption of NudC by CRISPR/Cas9 causes ciliary defects.

Click here for additional data file. (561.5KB, pdf)
Supplementary information, Figure S9

Cofilin 1 inhibits cilia assembly in HEK293T cells.

Click here for additional data file. (396.8KB, pdf)
Supplementary information, Figure S10

Exogenous expression of cofilin 1 mRNA rescues the ciliary defects in cofilin 1 morphants.

Click here for additional data file. (978.6KB, pdf)
Supplementary information, Figure S11

Cofilin 1 reverses the ciliary defects in zebrafish injected with NudC MO-2.

Click here for additional data file. (792.8KB, pdf)
Supplementary information, Figure S12

Disruption of cofilin 1 by CRISPR/Cas9 induces ciliary phenotypes.

Click here for additional data file. (558.3KB, pdf)
Supplementary information, Figure S13

Cofilin 1 partially rescues the enlarged pronephric duct in NudC morphants.

Click here for additional data file. (537.5KB, pdf)
Supplementary information, Figure S14

The cellular localization of NudC in RPE-1 cells.

Click here for additional data file. (461.6KB, pdf)
Supplementary information, Figure S15

Inhibition of Hsp90 activity suppresses ciliogenesis in mammalian cells.

Click here for additional data file. (315.8KB, pdf)
Supplementary information, Figure S16

Inhibition of Hsp90 activity has no significant effect on the protein level of cofilin 1.

Click here for additional data file. (182.9KB, pdf)
Supplementary information, Movie S1

Ciliary motility in pronephric duct of control morphant. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S2

Ciliary motility in pronephric duct of NudC morphant. Blue arrows indicate pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S3

Ciliary motility in pronephric duct of the embryo injected with NudC mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S4

Ciliary motility in pronephric duct of NudC morphant co-injected with NudC mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S5

Ciliary motility in pronephric duct of control morphant. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S6

Ciliary motility in pronephric duct of NudC morphant. Blue arrows indicate pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S7

Ciliary motility in pronephric duct of the embryo injected with cofilin 1 mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)
Supplementary information, Movie S8

Ciliary motility in pronephric duct of NudC morphant co-injected with cofilin 1 mRNA. Blue arrows show pronephric duct.

Click here for additional data file. (4.7MB, mpeg)

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