Published in Volume
123, Issue 12
(December 2, 2013)J Clin Invest.
Copyright © 2013, American Society for Clinical Investigation
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
1Division of Nephrology, Department of Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, Massachusetts, USA.
2Inserm U983, Necker Hospital, Paris, France.
3Université Paris Descartes, Sorbonne Paris Cité, Imagine Institute, Paris, France.
4Department of Chemistry and Biochemistry and Molecular Biology Institute, UCLA, Los Angeles, California, USA.
5Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
6Division of Nephrology, University Health Network, and University of Toronto, Toronto, Ontario, Canada.
7Department of Pathology, University Health Network, Toronto, Ontario, Canada.
8Program in Genomic Biology, Hospital for Sick Children, Toronto, Ontario, Canada.
9Bioinformatics Plateform, Université Paris Descartes, Paris, France.
10Genomics Plateform, Imagine Institute, Université Paris Descartes, Paris, France.
11Service de Néphrologie et Rhumatologie Pédiatrique, Centre de référence des maladies rénales rares, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Bron, France.
12Jules Stein Eye Institute, UCLA School of Medicine, Los Angeles, California, USA.
13Institute of Human Genetics, Helmholtz Zentrum Munich, Neuherberg, Germany.
14Institute of Human Genetics, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.
15Division of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
16Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, United Kingdom.
17Pediatrics Department, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
18Nottingham University Hospitals, Nottingham, United Kingdom.
19Children’s and Academic Renal Unit, University of Bristol, Bristol, United Kingdom.
20UCL Institute of Child Health and Paediatric Nephrology, Great Ormond Street Hospital, London, United Kingdom.
21Department of Pediatric Nephrology and Rheumatology, Gülhane Military Academy of Medicine, School of Medicine, Etlik, Ankara, Turkey.
22Biomedical Research Core Facilities and
23Department of Internal Medicine, Department of Pathology, and Department of Otolaryngology, University of Michigan, Ann Arbor, Michigan, USA.
24Department of Genetics, Howard Hughes Medical Institute, and
25Yale Center for Mendelian Genomics, Yale University School of Medicine, New Haven, Connecticut, USA.
26HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
27Department of Internal Medicine — Molecular Medicine and Genetics, University of Michigan, Ann Arbor, Michigan, USA.
28Department of Woman and Child Health, University of Padova and Istituto di Ricerca Pediatrica Città della Speranza, Padova, Italy.
29Assistance Publique – Hôpitaux de Paris, Department of Genetics, Necker Hospital, Paris, France.
30Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.
31Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Address correspondence to: Friedhelm Hildebrandt, Howard Hughes Medical Institute, Boston Children’s Hospital, 300 Longwood Avenue, HU319, Boston, Massachusetts 02115, USA. Phone: 617.355.6129; Fax: 617.730.0569; E-mail:
Friedhelm.Hildebrandt@childrens.harvard.edu. Or to: Corinne Antignac, Inserm U983 (ex-U574) and Department of Genetics, Necker Hospital, 149, rue de Sevres, 75015 Paris, France. Phone: 220.127.116.11.50.98; Fax: 18.104.22.168.02.90; E-mail:
firstname.lastname@example.org. Or to: York Pei, Division of Nephrology and of Genomic Medicine, University Health Network and University of Toronto, 8N838, 585 University Avenue, Toronto, Ontario, Canada M5G2N2. Phone: 416.340.4257; Fax: 416.340.4999; E-mail:
Authorship note: Shazia Ashraf and Heon Yung Gee contributed equally to this work.
First published November 25, 2013
Submitted: January 28,
2013; Accepted: September 6,
Identification of single-gene causes of steroid-resistant nephrotic syndrome (SRNS) has furthered the understanding of the pathogenesis of this disease. Here, using a combination of homozygosity mapping and whole human exome resequencing, we identified mutations in the aarF domain containing kinase 4 (ADCK4) gene in 15 individuals with SRNS from 8 unrelated families. ADCK4 was highly similar to ADCK3, which has been shown to participate in coenzyme Q10 (CoQ10) biosynthesis. Mutations in ADCK4 resulted in reduced CoQ10 levels and reduced mitochondrial respiratory enzyme activity in cells isolated from individuals with SRNS and transformed lymphoblasts. Knockdown of adck4 in zebrafish and Drosophila recapitulated nephrotic syndrome-associated phenotypes. Furthermore, ADCK4 was expressed in glomerular podocytes and partially localized to podocyte mitochondria and foot processes in rat kidneys and cultured human podocytes. In human podocytes, ADCK4 interacted with members of the CoQ10 biosynthesis pathway, including COQ6, which has been linked with SRNS and COQ7. Knockdown of ADCK4 in podocytes resulted in decreased migration, which was reversed by CoQ10 addition. Interestingly, a patient with SRNS with a homozygous ADCK4 frameshift mutation had partial remission following CoQ10 treatment. These data indicate that individuals with SRNS with mutations in ADCK4 or other genes that participate in CoQ10 biosynthesis may be treatable with CoQ10.
Nephrotic syndrome (NS) is a chronic kidney disease that is defined by significant proteinuria (>40 mg/m2/h), with resulting hypoalbuminemia, which causes edema (1). NS constitutes the second most frequent cause of end-stage kidney disease (ESKD) in children (2, 3). While most children with NS have steroid-sensitive NS, approximately 10%–20% of children and 40% of adults with NS do not achieve sustained remission after glucocorticoid therapy and additional immunosuppressive therapy and enter into ESKD (1). These cases of steroid-resistant NS (SRNS) manifest histologically as focal segmental glomerulosclerosis (FSGS) (4).
Recent discoveries of the single-gene causes of NS have significantly increased our understanding of glomerular filtration barrier physiology and of pathogenic mechanisms of NS (1). To date, more than 9 recessive genes that cause NS if mutated have been identified (5, 6). Overall, these genes account for up to approximately 66% of NS that starts within the first year of life (2). However, monogenic causes of a significant proportion of childhood- or adult-onset NS are still molecularly unsolved. Moreover, recently identified genes are very rare, being mutated in only one family out of hundreds (7). To overcome the limitations posed by the rarity of genes when identifying genes associated with NS, we established a strategy of combining homozygosity mapping (HM) with whole-exome resequencing (WER) (8, 9). Here, we applied this approach to sibling cases of childhood-onset NS and thereby identified mutations of aarF domain containing kinase 4 (ADCK4) as a single-gene cause of SRNS.
Mutations in ADCK4 cause SRNS. To identify further single-gene causes of SRNS, we performed HM followed by WER in a group of individuals with histology that revealed FSGS (Figure 1, A and B). In a family (A2338) of Arab origin, 2 siblings had early-onset SRNS and renal histology that revealed glomerulosclerosis (Figure 1A). HM in both affected siblings yielded 5 regions of homozygosity by descent with a cumulative genomic length of approximately 115 Mb, none of which coincided with any of 7 common recessive causes of SRNS (Figure 1C). The presence of homozygosity strongly suggested a recessive causative gene, and the lack of overlap with known NS gene loci suggested that the gene to be identified in this family would be novel. By WER in one of the affected siblings from family A2338, we detected a homozygous missense mutation (c.532C>T;p.R178W) in ADCK4 (NM_024876.3) on chromosome 19, encoding ADCK4. This variant was the only homozygous variant remaining from the variant filtering process (Supplemental Table 1; supplemental material available online with this article; doi:
10.1172/JCI69000DS1). The mutation (p.R178W) alters an amino acid residue conserved throughout evolution from Chlamydomonas reinhardtii. It segregated with the affected status in this family and was absent from >190 ethnically matched healthy control individuals and from >8,600 European controls in the Exome Variant Server (
HM and exon capture resequencing reveal ADCK4 mutations as causes of SRNS.
(A) Renal histology of individual A2338-21 reveals global glomerulosclerosis by excess PAS staining (red). Original magnification, ×200. (B) Renal histology of individual Pt5496 shows cFSGS. PAS staining (left) reveals retraction and collapse of the capillary tuft, with numerous foam cells and groups of hyperplastic and vacuolated visceral epithelial cells. Original magnification, ×40. Electron microscopy image (right) shows foot process effacement (black arrowheads). In addition, capillary basement membranes are thickened and remodeled. Original magnification, ×15,000. (C) Nonparametric LOD (log of the odds ratio) (NPL) score profile across the human genome in 2 siblings with SRNS of consanguineous family A2338. Five maximum NPL peaks (red circles) indicate candidate regions of homozygosity by descent. ADCK4 is positioned (arrowhead) within a peak on chromosome (Chr) 19. Numbers at the bottom of the panels are measured in centimorgan (cM). (D) Exon structure of human ADCK4 cDNA. ADCK4 contains 15 exons. Positions of start codon (ATG) and of stop codon (TGA) are indicated. (E) Domain structure of ADCK4. The helical, ABC1, and kinase domains are depicted by colored bars in relation to encoding exon position. (F) Eleven different ADCK4 mutations in eight families with SRNS. Family numbers and amino acid changes (Table 1) are given above sequence traces. Arrowheads denote altered nucleotides. Lines and arrows indicate positions of mutations in relation to exon D and protein domain E. (G) For the 5 missense mutations (p.R178W, p.D286G, p.R320W, p.R343W, and p.R477Q) conservation across evolution of altered amino acid residues is shown.
WER in an addtional 6 different families with SRNS also yielded 9 additional mutations in ADCK4 (3 families with homozygous mutations and 3 families with compound heterozygous mutations) (Figure 1, D–G, and Table 1). WER of one affected individual in family 386 identified compound heterozygous mutations: c.101G>A;p.W34* and c.954_956dup;p.T319dup. We identified compound heterozygous mutations (c.645delT;p.F215Lfs*14 and c.4130G>A;p.R477Q in ADCK4) in 2 affected siblings from family 231 from Algeria (Figure 1F and Table 1). The missense mutation (p.R477Q) altered an amino acid residue that was continually conserved from C. reinhardtii to humans (Figure 1G). In a family (A5170) of 3 affected siblings, WER revealed compound heterozygous mutations: c.857A>G;p.D286G and c.1447G>T;p.E483* in ADCK4 (Figure 1F and Table 1). This missense mutation (p.D286G) altered an amino acid residue that is continually conserved from C. reinhardtii to humans (Figure 1G). One of the homozygous mutations (p.R320W) in ADCK4 was found in 2 affected siblings from the ABD family from Tunisia in an amino acid residue continually conserved throughout evolution from C. reinhardtii (Figure 1, F and G, and Table 1). In another family (Mek) from Morocco, we discovered a missense mutation c.1027C>T;p.R343W in this gene in 2 affected siblings (Figure 1F and Table 1). The amino acid residue R343 has been conserved from C. reinhardtii to humans (Figure 1G). The other homozygous mutation was an out-of-frame deletion of 7 bases (p.Q452Hfs) in exon 15 of ADCK4 in 2 affected siblings from a family from India, with renal histology showing collapsing FSGS (cFSGS) (Figure 1F and Table 1).
Recessive ADCK4 mutations detected in individuals with SRNS
To discover additional mutations in ADCK4, we then performed multiplex barcoded array-based PCR amplification and next-generation sequencing in an additional 400 individuals with SRNS (10). In an individual with SRNS (A4169-21), we detected a homozygous insertion of an “A” (H400Nfs*11) in exon 13 of ADCK4 (Figure 1F and Table 1). Sequences of primers used to amplify exons and exon-intron boundaries of ADCK4 are listed in Supplemental Table 2. All 15 affected individuals of the 8 families with recessive mutations in ADCK4 had SRNS. Renal biopsy revealed FSGS in most cases. Interestingly, in 3 affected individuals (1146, Pt5497, and Pt5497), renal histology showed cFSGS (Figure 1B and Table 1). Moreover, the individual A4169-21, who has a homozygous truncating allele, showed the earliest onset of SRNS and also presented with developmental delay (Table 1).
ADCK4 spans 12 kb on chromosome 19q13.1. Up to 17 different putative alternatively spliced ADCK4 transcripts encoding different proteins have been proposed (AceView;
http://www.ncbi.nlm.nih.gov/ieb/research/acembly/index.html). The longest transcript of ADCK4 (NM_024876.3) has 14 coding exons (Figure 1D) and encodes a 60.1-kDa protein (NP_079152.3, isoform a, 544 amino acids) (Figure 1E). Analysis of the ADCK4 amino acid sequence yielded a helical domain and an ABC1 domain and a kinase domain (Figure 1E). ADCK4 has high sequence similarity to Abc1/Coq8 and is evolutionarily conserved to Ciona intestinalis (sea squirt) (XP_002126787.1), Drosophila melanogaster (NP_572836.1), Caenorhabditis elegans (NP_498014.2), C. reinhardtii (XP_001702520.1), and Saccharomyces cerevisiae (NP_011396.1), suggesting a conserved function of the domain assembly.
Knockdown of adck4 in animal models recapitulates the nephrosis phenotype. To further validate the causative role of ADCK4 for the SRNS phenotype, we performed knockdown of the ADCK4 ortholog in zebrafish. For zebrafish gene knockdown experiments, we used a p53 morpholino oligonucleotide (MO) as a negative control to minimize nonspecific apoptotic MO effects (11). p53 MO injection into fertilized zebrafish eggs at the 1- to 4-cell stage did not produce any phenotype through 168 hours postfertilization (hpf) (Figure 2A). However, coinjection of the p53 control MO with an MO targeting the translation initiation site of zebrafish adck4 caused the nephrosis phenotype of periorbital and total body edema, reminiscent of signs of NS in humans, in 54.1% of embryos at 120 hpf (Figure 2B). Similar results were obtained with 2 MOs targeting the splice donor site (e2i2 MO and e3i3 MO) (Figure 2C; Supplemental Figure 1, A–D; and Supplemental Table 3). The summary of edema phenotype observed in adck4 morphants is displayed in Supplemental Figure 1E. The proteinuric effect of the adck4 MO was confirmed using an established zebrafish proteinuria assay (12) by ELISA against a fusion protein of vitamin D–binding protein and GFP in l-fabp::VDBP-GFP transgenic zebrafish (Figure 2D). We then performed transmission electron microscopy imaging of zebrafish to permit a more direct evaluation of glomerular structures of morphants. When compared with the control (Figure 2E), we observed upon knockdown of adck4 characteristic alterations of nephrosis (Figure 2E). These included podocyte foot process effacement and disorganization, rarefaction of slit membranes, and disorganization of the glomerular basement membranes in zebrafish glomeruli (Figure 2E, black arrowheads in right panel), as previously described in plce1 knockdown (13).
Functional analysis of adck4 knockdown in zebrafish.
(A) Control zebrafish were injected with p53 MO (0.2 mM) as a control to minimize nonspecific MO effects. p53 MO was injected into fertilized eggs at the 1- to 4-cells stage and did not produce any phenotype up to 168 hpf (n >100). Scale bar: 0.5 mm. (B) Zebrafish coinjected with adck4 ATG MO (0.2 mM) targeting the translation initiation site of zebrafish adck4 and with p53 MO. At 120 hpf, adck4 morphants display the nephrosis phenotype of periorbital edema (arrows) and total body edema in 54.1% (193 out of 357) of embryos. (C) Zebrafish coinjected with adck4 e3i3 MO (0.2 mM) targeting the donor site of intron 3 of zebrafish adck4 and with p53 MO. At 120 hpf, adck4 morphants display the nephrosis phenotype (arrows) in 48.3% (274 out of 567) of embryos. Scale bar: 1 mm (B and C). (D) Proteinuria assay by ELISA against a fusion protein of vitamin D–binding protein and GFP in l-fabp::VDBP-GFP transgenic zebrafish. Note that knockdown of adck4 causes significant proteinuria compared with that in control fish injected with p53 MO only. (P < 0.001). Symbols indicate each measurements; horizontal bars indicate the average; data are presented with the average ± SEM denoted by 3 horizontal lines. (E) Electron microscopic ultrastructure of GBM and podocyte foot processes in p53 MO control and adck4 morphant zebrafish. In the control zebrafish, the foot processes are regularly spanned by slit diaphragms (black arrowheads). In contrast, the foot processes of the morphants are effaced and disorganized (black arrowheads). Scale bar: 2 μm.
In addition, we performed knockdown of Drosophila coq8 (dcoq8) in Drosophila pericardial nephrocytes, which share remarkable similarities to the glomerular podocytes (14). The protein uptake assay showed that knockdown of dcoq8 in nephrocytes reduced the uptake ability of a secreted fusion protein of rat atrial natriuretic factor (ANF) and GFP, suggesting that dcoq8 is required for nephrocyte function in Drosophila (Supplemental Figure 2, A and B). The amino acid of dCoq8 has 53% sequence identity to both ADCK3 and ADCK4 Drosophila (Supplemental Figure 2C).
ADCK4 localizes to the mitochondria and foot processes in podocytes. Since most gene products that are defective in SRNS are located in glomerular podocytes, we examined the subcellular localization of ADCK4 in adult rat kidney by immunofluorescence (IF). Podocytes, as identified by expression of nuclear WT1, expressed ADCK4 at high levels in cell bodies and primary processes (Figure 3A). ADCK4 also partially colocalized with cytochrome oxidase subunit VI (COXIV) and mitochondrially encoded cytochrome c oxidase 1 (MTCO1), 2 known mitochondrial marker proteins, suggesting that ADCK4 partly localizes to the mitochondria in renal glomeruli (Figure 3, B and C). In addition, ADCK4 is detected in proximal tubules and collecting ducts (Supplemental Figure 3, A and B). To further investigate the localization of ADCK4, we performed immunogold electron microscopy in adult rat kidneys. In podocytes, ADCK4 was predominantly detected at foot processes (Figure 3D). The specificity of the anti-ADCK4 antibody used in the IF and immunogold electron microscopy studies is demonstrated in Supplemental Figure 4. We also examined the expression of ADCK4 in cultured podocytes by IF. The overexpressed ADCK4–red fluorescent protein (ADCK4-RFP) partially colocalized to mitochondria, and we also noticed that ADCK4-RFP localized to ruffles (Figure 3E) of podocytes, the equivalents of foot processes (Figure 3E and Supplemental Figure 3, C and D). Consistent with data from the cellular fractionation of cultured podocytes, these findings showed that ADCK4 is endogenously present in both the cytosolic and mitochondrial fractions (Figure 3F). Thus, in addition to its role in the mitochondrial respiratory chain, ADCK4 seems to have a very localized function at ruffles and foot processes of podocytes.
ADCK4 localizes to the mitochondria and cytoplasm of podocytes in adult rat glomeruli and also in cultured human podocytes. (A–C) Coimmunofluorescence of ADCK4 with (A) WT1 as well as (B) MTCO1 and (C) COXIV in adult rat glomeruli. ADCK4 partially colocalizes to mitochondria with the 2 mitochondrial markers COXIV and MTCO1. Scale bar: 10 μm. (D) Immunogold electron microscopy of adult rat kidney displays localization of ADCK4 (black arrowheads) at podocyte foot processes of glomeruli. A control without a primary antibody is shown on the left. Scale bar: 1 μm; ×2.5 (inset). (E) Podocytes were transfected with ADCK4-RFP and stained with an anti-COXIV antibody. ADCK4 partially colocalizes to mitochondria with COXIV. Note that ADCK4 also localizes along the plasma membrane (white arrowheads) in podocytes. Scale bar: 25 μm. (F) Subcellular fractionation of ADCK4 in undifferentiated and differentiated podocytes. Mitochondrial and cytosol fractions were prepared and immunoblotted for ADCK4, MTCO1, and COXIV, respectively. Each lane was loaded with 50 μg protein. Note that ADCK4 is present in both mitochondrial (marked by MTCO1 and COXIV), and cytosolic fractions in both undifferentiated and differentiated podocytes. W, whole cell lysates; Cyto, cytosol fraction; MT, mitochondrial fraction.
ADCK4 is enriched in podocytes and interacts with COQ6 and COQ7. By quantitative real-time PCR, we showed that, although ADCK3 expression exceeds that of ADCK4 in most human tissues (Supplemental Figure 5), ADCK4 is enriched in both differentiated and undifferentiated human podocytes (Figure 4A).
ADCK4 is enriched in podocytes and interacts with COQ6 and COQ7. (A) Relative expression of ADCK3 and ADCK4 in kidney tissue and podocytes, as measured by quantitative real-time PCR. Error bars indicate SD of 4 experiments. (B) Interaction of ADCK4 with COQ6 and COQ7 in cultured human podocytes. A C-terminally V5-tagged COQ6 construct (COQ6-V6) was transfected into the undifferentiated cultured podocytes. Coimmunoprecipitation was performed using an anti-V5 antibody and then blotting was performed with antibodies for ADCK4, COQ6, and COQ7. Note that the protein complex precipitated by COQ6 includes COQ7 and ADCK4. (C) Interaction of endogenous ADCK4 and COQ6 in differentiated podocytes. Podocyte lysates were precipitated with an anti-ADCK4 antibody or a control rabbit IgG. The precipitated proteins were separated by SDS-PAGE and blotted with an anti-COQ6 antibody.
Furthermore, we performed coimmunoprecipitation studies in cultured podocytes to examine whether ADCK4 interacts with other proteins like COQ6 and COQ7 that are involved in the coenzyme Q10 (CoQ10) biosynthesis pathway. COQ6 was overexpressed in podocytes, and coimmunoprecipitation was performed. Interestingly, the protein complex precipitated by COQ6 included COQ7 and ADCK4 (Figure 4B). We also confirmed that ADCK4 and COQ6 interact endogenously in lysates from differentiated podocytes (Figure 4C).
Levels of CoQ10 are decreased in individuals with ADCK4 mutations.
To investigate whether the defect in ADCK4 has any effect on CoQ10 biosynthesis, we measured the total CoQ10 contents in EBV-transformed lymphoblasts or cultured skin fibroblasts derived from individuals from the A2338, A4169, and Pt5496/Pt5497 families, in which ADCK4 mutations were detected. In the case of the A2338 and A4169 families, the total CoQ10 was found to be strongly reduced in the affected siblings, A2338-21 (81.92 ± 18.45 pmol/mg protein) and A2338-22 (75.99 ± 34.60 pmol/mg protein), who have a homozygous missense mutation (p.R178W), and in an affected individual, A4169-21 (59.12 ± 9.57 pmol/mg protein), who has a homozygous frameshift mutation (p.H400Nfs*11) (Figure 5A). In contrast, the unaffected individuals, A2338-26 and A2338-27, who have both wild-type alleles, had 784.40 ± 164.10 and 758.00 ± 286.60 pmol/mg protein of total CoQ10, respectively (Figure 5A).
CoQ10 content in EBV-transformed lymphoblasts and fibroblasts from SRNS families with mutations in ADCK4.
(A) Scatter plot showing the total CoQ10 content in EBV-transformed lymphoblasts derived from either healthy or affected individuals from the A2338 and A4169 families. Individuals A2338-21, A2338-22, and A4169-21 are affected with SRNS, while A2338-26 and A2338-27 have both wild-type alleles. The content of CoQ10 is presented with the average ± SD denoted by 3 horizontal lines (n = 4; except n = 6 for A4169-21). The content from A2338-26 is significantly higher than the CoQ10 content from A2338-21, A2338-22, and A4169-21 (multiple comparison, P < 0.0001). Symbols indicate individual lymphoblasts; horizontal bars indicate the average. (B) Scatter plot showing the total CoQ10 content in fibroblasts derived from either healthy parents or affected individuals (Pt5496 and Pt5497). The content of CoQ10 is presented with the average ± SD denoted by 3 horizontal lines (n = 8). CoQ10 content from #50551 is statistically lower than CoQ10 content from #50550 (multiple comparison, P = 0.0134) and significantly higher than the CoQ10 contents from #50552 and #50553 (multiple comparison, P < 0.0001). Symbols indicate individual fibroblasts; horizontal bars indicate the average. (C) In vivo maximal uncoupled OCR over the whole respiratory chain, including the Q10 transfer of electrons from mitochondrial complex I and complex II to complex III. Maximal respiration was significantly reduced in fibroblasts from Pt5496 and Pt5497 compared with that in control fibroblasts. Data shown are mean ± SD (n > 10). *P < 0.001.
Likewise, in the case of Pt5496 and Pt5497, we confirmed similar results and found that the total CoQ10 was reduced in fibroblasts (20.11 ± 3.41 pmol/mg protein for #50552 and 19.75 ± 4.63 pmol/mg protein for #50553) from these individuals, who have a homozygous frameshift mutation (p.Q452Hfs), and normal in fibroblasts (64.33 ± 11.92 pmol/mg protein for #50551 and 83.04 ± 20.64 pmol/mg protein for #50550) from the unaffected parents (Figure 5B).
In addition, we examined mitochondrial respiratory enzyme activity in fibroblasts by measuring maximal uncoupled oxygen consumption rate (OCR), which shows the CoQ10 transfer of electrons from mitochondrial complex I and complex II to complex III. Maximal OCR was significantly reduced in fibroblasts from Pt5496 and Pt5497 compared with that in fibroblasts from controls or their healthy parents (Figure 5C).
Loss of ADCK4 does not induce proliferation or apoptosis in fibroblasts or cultured podocytes. We had previously reported that knockdown of COQ6 can cause apoptosis in podocytes (7). Since ADCK4 interacts with COQ6, we investigated the effect of loss of ADCK4 on cell proliferation and apoptosis in fibroblasts from individuals with a homozygous frameshift ADCK4 mutation (Pt5496 and Pt5497) and their healthy parents as well as in cultured podocytes. We found that fibroblasts (#50552 and #50553) from affected individuals did not show any difference in cell proliferation or apoptosis induced by hydrogen peroxide compared to parental fibroblasts (#50550 and #50551) (Supplemental Figure 6, A and B). Furthermore, in contrast to COQ6, knockdown of ADCK4 in podocytes did not affect proliferation or apoptosis (Supplemental Figure 6, C and D).
ADCK4 knockdown reduces podocyte migration, which is reversed by the addition of CoQ10.
We next examined the effect of ADCK4 knockdown on podocyte migration using the xCELLigence system, which monitors cell migration in real-time (Figure 6). We found that migration of podocytes was reduced by knockdown of ADCK4 (Figure 6A). Because CoQ10 treatment had resulted in improvement of the NS phenotype in an individual with a mutation in ADCK4, we tested the effect of the addition of CoQ10 on podocyte migration. Interestingly, we found that the addition of CoQ10 reversed the decreased migratory phenotype caused by ADCK4 knockdown (Figure 6, A and B). Similar results were obtained when 2 additional siRNAs were used for knockdown of ADCK4 in cultured human podocytes (ADCK4 siRNAs #5 and #6) (Figure 6, C and D). We further found that decreased migration, which was caused by an ADCK4 siRNA (ADCK4 siRNA #6), was reversed when wild-type mouse ADCK4 was transfected into podocytes (Figure 6C). This result also confirmed that the effect on podocyte migration was caused by ADCK4 loss of function.
Knockdown of ADCK4 decreases the migratory phenotype of podocytes. (A) The effect of ADCK4 knockdown on podocyte migration. Podocytes transfected with ADCK4 siRNA (red) exhibited decreased migration compared with podocytes transfected with scrambled siRNA (black). The decrease in podocyte migration was partially reversed by the addition of 50 μM CoQ10 (green). Error bars are shown in only one direction for clarity and indicate SDs from 3 independent experiments. (B) The efficiency of ADCK4 siRNA used in A was confirmed by immunoblotting with an anti-ADCK4 antibody and an anti–β-actin antibody. (C) Transfection of podocytes with 2 additional ADCK4-specific siRNAs (siRNA #5 and #6) confirmed the result from A that ADCK4 knockdown in human podocytes reduces migration (red dotted and solid lines) compared with podocytes transfected with the scrambled siRNA (black). The decrease in podocyte migration by ADCK4 knockdown using ADCK4 siRNA #6 was rescued by transfection of mouse Adck4 construct (green). Mouse ADCK4 has 5 mismatches from the siRNA target sequences. Error bars indicate SDs of 3 independent experiments. (D) The efficiency of ADCK4 siRNAs used in C was confirmed by immunoblotting. 100 nM of each siRNA was transfected into podocytes.
Here, we describe the discovery of mutations in ADCK4 as causes of SRNS. We have shown that ADCK4 is expressed in podocytes and localizes to mitochondria and foot processes and interacts with COQ6 endogenously. Knockdown of ADCK4 in podocytes reduced their migration phenotype, which could be reversed by overexpression of siRNA-resistant ADCK4 or, most importantly, by the addition of CoQ10. By knockdown of adck4 in zebrafish, we clearly demonstrated that the function of this gene is necessary to avoid the NS disease phenotype. The fact that ADCK4 has high sequence similarity with ADCK3, which was previously reported to be associated with CoQ10 deficiency (15), and the fact that cells from affected individuals with ADCK4 mutations (families A2338, A4169, and Pt5496/Pt5497) had reduced total CoQ10 content suggests that ADCK4 is also involved in CoQ10 biosynthesis.
CoQ10, also known as ubiquinone, is a lipid-soluble component of virtually all cell membranes, in which it is thought to play an important antioxidant role as well as to transport electrons from complexes I and II to complex III in the respiratory chain of the mitochondrial inner membrane (16). The biochemical pathway of CoQ10 biosynthesis is complex and has not been completely elucidated. Primary CoQ10 deficiencies due to mutations in ubiquinone biosynthetic genes (COQ2, COQ4, COQ6, PDSS1, PDSS2, and ADCK3) have been identified (7, 15, 17–26). Clinical manifestations of CoQ10 deficiency are variable. For example, individuals with COQ2 mutations present with phenotypes ranging from isolated NS to catastrophic neonatal multisystem disorder with encephalomyopathy and renal involvement to a recently described multiple-system atrophy (20, 23–27). In addition, COQ6 (7) and PDSS2 (19) have also been implicated in the cause of SRNS.
We as well as Montini et al. have shown previously that the individuals affected with SRNS due to mutations in CoQ10 biosynthesis pathway genes like COQ2 and COQ6 can be treated with the innocuous food supplement CoQ10 (7, 28). CoQ10 deficiency in individuals with ADCK4 mutations thus raises the possibility of supplementation therapy. So far, only one individual (A4169-21) with ADCK4 mutation has been treated with CoQ10 (15 mg/kg/d) for over 4 years. He was first treated with intravenous methylprednisolone followed by 2 mg/kg/d prednisolone over 10 weeks without achieving remission of NS. Subsequently, he was treated with 2 mg/kg/d cyclophosphamide for 3 months. The treatment resulted in partial remission, but treatment had to be stopped because of infections. Treatment with CoQ10 was commenced at 1 year of age, giving 100 mg/d CoQ10 orally together with 5 mg of prednisolone every other day. Then, the edema disappeared and proteinuria decreased significantly. The individual is currently being treated with CoQ10 (15 mg/kg/d) with captopril (12.5 mg/d). Even though the effectiveness of CoQ10 treatment cannot be generalized for individuals with ADCK4 mutations at the moment based on this single case, we still think that the identification of molecular defects of CoQ10 biosynthesis is important because they may represent forms of SRNS that are treatable by administration of CoQ10.
ADCK3 and ADCK4 are highly similar members of an ancient atypical kinase family and appear to result from gene duplication in vertebrates (15). The yeast Coq8/Abc1 is required for CoQ biosynthesis (29) and is essential for the organization of high-molecular-mass Coq polypeptide complex and for phosphorylated forms of the Coq3, Coq5, and Coq7 polypeptides that perform methylation and hydroxylation steps in CoQ biosynthesis (30, 31). Considering their similarity, it is interesting that mutations in ADCK3 result in cerebellar ataxia and seizures without renal involvement (15, 21), whereas mutations in ADCK4 cause SRNS mostly without neurological symptoms. Currently, there is no clear explanation for this; however, this may be partially due to their differential tissue expression (Figure 4A and Supplemental Figure 5). Xie et al. previously showed that ADCK3 can rescue yeast coq8 mutants and restore phosphorylated forms of yeast Coq polypeptides (30), but the same group observed that expression of ADCK4 failed to rescue coq8 mutants (data not shown). On the other hand, knockdown of Dcoq8, which has 53% amino acid identity to both ADCK3 and ADCK4, caused defects in nephrocyte function (Supplemental Figure 2). Overall, these results suggest that ADCK3 and ADCK4 are independently required for synthesis of CoQ, yet retain distinct functions, a difference that may have evolved in vertebrates, and that ADCK3 may be closer to yeast Coq8.
cFSGS is defined morphologically by the presence of hyperplastic and hypertropic podocytes overlying collapsed capillary loops within glomerular tufts (32). Interestingly, the histology of affected individuals (1146, Pt5496, and Pt5497) with ADCK4 mutations showed cFSGS. In addition, mutant kd/kd mice, which have a missense mutation in Pdss2 and present with isolated nephropathy, have features of cFSGS (33). Therefore, it will be important to investigate whether nephropathy resulting from CoQ10 deficiency results in cFSGS, because this may be a phenotypic criterion with which to choose individuals with SRNS that should be screened for genes involved in CoQ10 biosynthesis, such as COQ2, COQ6, PDSS2, and ADCK4. To answer this, it is necessary to investigate more SRNS cases resulting from CoQ10 deficiency. In addition, knockout animal models for Coq2, Coq6, and Adck4 will be helpful.
In conclusion, we identified recessive mutations in ADCK4 as novel single-gene causes of SRNS. Early recognition of this new genetic entity of SRNS will be important because it may represent a form of SRNS that can potentially be treated by CoQ10 supplementation.
Subjects. Following informed consent, we obtained clinical data and blood samples from individuals with SRNS or steroid-sensitive NS from worldwide sources. The diagnosis of NS was made by (pediatric) nephrologists based on standardized clinical and renal histological criteria (34). Renal biopsies were evaluated by renal pathologists. Clinical data were obtained using a standardized questionnaire (
HM, WER, and mutation calling. For the A2338 family, HM, WER, and mutation calling were performed as described previously (35). HM in the 231 and ABD families was performed using Human Mapping 250k NspI Array (Affymetrix), and parametric logarithm of odds (LOD) scores were calculated with MERLIN (36). For WER of the 231, ABD, and Mek families, DNA was processed using All Exon 50Mb V3 (Agilent SureSelect) to enrich for exonic sequences and a SOLiD 5500XL high-throughput sequencing machine (Applied Biosystems) (paired-end reads: 50 bases forward, 25 bases reverse). Obtained sequences were aligned to the human genome (NCBI build 37/hg19) using Lifescope suite from Lifetech. Substitution and variation calls were made with the GATK pipeline (mpileup, bfctools, vcfuitil). Variants were then annotated with an in-house software (Polyweb), which allows users to set up bioinformatic filters in order to identify the putative mutation.
Plasmids, cell culture, and transfection. A human ADCK4 clone was purchased from Open Biosystems (clone accession BC013114.1). The mutant clones of ADCK4 were generated by a PCR-based site-directed mutagenesis method. The COQ6 clones were described previously (7). The immortalized human podocytes (37) were maintained in RPMI plus GlutaMAX-I (Gibco) supplemented with 10% FBS, penicillin (50 IU/ml)/streptomycin (50 μg/ml), and Insulin-Transferrin-Selenium-X (Invitrogen). Plasmids and siRNA were transfected into podocytes using Lipofectamine 2000 (Invitrogen). The ADCK4-specific and control scrambled siRNAs were purchased from Dharmacon or Sigma-Aldrich. Lymphoblasts were purified from blood samples using Ficoll-Paque PLUS (GE Healthcare) according to the manufacturer’s instructions. The isolated lymphoblasts were transformed by EBV and immortalized as described previously (38). Human fibroblasts were grown in DMEM supplemented with 15% FBS, penicillin (50 IU/ml)/streptomycin (50 μg/ml), and nonessential amino acids (Invitrogen).
Immunoblotting, immunoprecipitation, and IF staining. These experiments were performed as described previously (13). Anti-ADCK4 (LSBio), anti-MTCO1 (Abcam), anti-COXIV (Abcam), anti-COQ6 (Santa Cruz Biotechnology Inc.), anti-COQ7 (Proteintech), and anti-V5 (Invitrogen) were used. Fluorescent images were obtained with a Leica SP5X laser scanning microscope.
Immunogold electron microscopy. Rat renal cortex samples were dissected and trimmed into 1-mm-thick blocks, which were fixed by immersion in 4% formaldehyde and 0.5% glutaraldehyde in 0.1 M cacodylate buffer, pH 7.4, and processed for embedment in LR White. Semithin sections (700 nm) were first obtained to locate areas that contained glomeruli. Subsequently, ultrathin sections (70 nm) were obtained from those areas and collected on formvar-coated nickel grids and etched with saturated sodium periodate for 15 minutes. Sections were blocked with 0.1 M phosphate buffer, pH 7.4, containing 1% BSA, 3% goat serum, and 0.05% Tween-20 for 1 hour at room temperature and incubated with a rabbit anti-ADCK4 antibody (LSBio) in buffer overnight at 4°C. Sections were then washed and incubated with goat anti-rabbit IgG conjugated to 18 nm gold (Jackson ImmunoResearch Laboratories) and stained with uranyl acetate. Sections in which the primary antibody was omitted during the overnight incubation were used as negative control. Sections were observed on a Zeiss 910 transmission electron microscope.
Mitochondrial fractionation. The mitochondrial fractionation of podocytes was done using Mitochondrial Isolation Kit for Cultured Cells (Thermo Scientific), Mitochondrial/Cytosol Fractionation Kit (Abcam), and Mitochondrial Fractionation Kit (Active Motif) according to the manufacturer’s instructions.
Podocyte migration and proliferation assay. Real-time migration assays were performed using the xCELLIgence system (ACEA Biosciences) according to the manufacturer’s instructions. For migration assays, 24 hours after transfection, 4 × 104 cells were plated with serum-free media in the upper chamber of the CIM-plate 16 (ACEA Biosciences). The lower chambers were filled with 10% FBS for chemoattraction or with serum-free media. For proliferation assays, 4 × 104 cells were plated with serum-free media in the E-plate 16 (ACEA Biosciences). The data obtained were analyzed with RTCA software. Results are presented as the time versus cell index curve.
Zebrafish studies. Zebrafish (Danio rerio) were maintained and reared as described previously (12). Approval for zebrafish research was obtained from the University of Michigan and the Boston Children’s Hospital Committees on the Use and Care of Animals. MOs were injected into the AB* wild-type strain for phenotype analysis of morphants and transmission electron microscopy. The proteinuria assays were performed using l-fabp::VDBP-GFP transgenic fish and the GFP ELISA Kit (Cell Biolabs) as described previously (12).
Cells (approximately 0.1 g) were thawed on ice and resuspended in 1.5 ml phosphate-buffered saline (0.14 M NaCl, 12.0 mM NaH2PO4, 8.1 mM Na2HPO4, pH 7.4), followed by homogenization with a polytron (Kinematica PT 2500E) for 1 minute at 15,300 g on ice. Lipid extracts were prepared by addition of 1.2 ml methanol, followed by 1.8 ml petroleum ether. Diethoxy-CoQ10 served as an internal standard (39). A typical standard curve contains 5 standards with 7.2 pmol, 20 pmol, 72 pmol, 140 pmol, and 400 pmol of CoQ10, respectively. Standard curve samples and experimental samples shared identical extractions. Each of the extraction tubes were vortexed for 45 seconds. The upper layer was removed, and the lower aqueous phase was reextracted with 1.8 ml petroleum ether. Nitrogen gas dried the combined organic phase, and 200 μl ethanol dissolved the dried lipids (USP, Apaer Alcohol and Chemical Co.). A binary HPLC solvent delivery system with a Luna Phenyl-Hexyl column (particle size 3 μm, 50 × 2.00 mm; Phenomenex) coupled with an Applied Biosystems 4000 QTRAP linear MS/MS spectrometer determined the total CoQ10 content. The mobile phase consisted of solvent A (methanol/isopropanol, 95:5, with 2.5 mM ammonium formate) and solvent B (isopropanol, with 2.5 mM ammonium formate). The percentage of solvent B started at 0% for the first 1.5 minutes, increased linearly to 15% by 2 minutes, remained constant for the next 1 minute, and decreased linearly back to 0% by 4 minutes. The flow rate remained constant at 600 μl/min. Data acquisition and processing required Analyst software (version 1.4.2). Multiple-reaction monitoring mode detected quinone content, with the following transitions: mass-to-charge [m/z] ratio 880.7:197.0 (CoQ10 with ammonium adduct); m/z 882.7:197.0 (Q10H2 with ammonium adduct); m/z 908.7:225.1 (diethoxy-Q10 with ammonium adduct), and m/z 910.7:225.1 (diethoxy-Q10H2 with ammonium adduct).
Mitochondrial respiratory enzyme activity measurement. Fibroblasts derived from controls (NHDF-neo, Bio-Rad), healthy parents, or 2 affected individuals (Pt5496 and Pt5497) were seeded at 20,000 cells per well in 80 ml DMEM and incubated at 37°C, 5% CO2 for 24 hours. In vivo maximal uncoupled OCR over the whole respiratory chain, including the CoQ10 transfer of electrons from mitochondrial complex I and complex II to complex III, was measured using the XF96 Extracellular Flux Analyzer (Seahorse Bioscience) (40). Mitochondria membrane potential was uncoupled by the addition of carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone (FCCP, 0.4 μM). Nonmitochondrial respiration was determined after the addition of 2.5 μM rotenone/5 μM antimycin A.
RNAi-based Drosophila nephrocyte functional assay. The MHC-ANF-RFP transgenic flies were generated in previous studies (14, 41). Nephrocyte-specific gene knockdown was achieved by using nephrocyte-specific Gal4 and UAS-RNAi transgenes (14, 41). Nephrocyte function was measured by the amount of secreted red fluorescent proteins accumulated in nephrocytes at the second instar larvae stage (14, 41). Hand-GFP (42) was used to label the cardiac nephrocytes.
Statistics. Results are presented as mean ± SEM or SD for the number of experiments indicated in the figure legends. Statistical analysis of continuous data was performed with 2-tailed Student’s t test or multiple comparison, as appropriate. P < 0.05 was considered statistically significant.
Study approval. Approval for research in human subjects was obtained from the IRBs of the University of Michigan, Boston Children’s Hospital, Université Paris Descartes, University of Toronto, Yale University, and Beth Israel Deaconess Medical Center.
The authors thank the families who contributed to this study. This research was supported by grants from the NIH to F. Hildebrandt (DK076683, DK086542), to R.C. Wiggins (DK46073 and DK081943), to E.A. Otto (DK090917), to W. Zhou (DK091405), to Z. Han (R01HL090801), to D.S. Williams (EY07042), and to R.P. Lifton (U54HG006504); by the Kidney Foundation of Canada and Nephcure Canada (to A.D. Paterson and Y. Pei); by the Nephcure Foundation (to F. Hildebrandt and M. Pollak); by the National Research Foundation (Basic Science Research Program funded by the Ministry of Education, Science and Technology) (to H.Y. Gee, 2012R1A6A3A03040212); by the American Heart Association (to Z. Han, AHA-0630178N); by the Association Francaise contre les Myopathies (to C. Antignac, GLOMGENE project: ANR-08-GENOPAT-017-01); by the Fondation pour la Recherche Medicale (to C. Antignac, project DMP 2010-11-20-386); by the European Community’s 7th Framework program grant (to C. Antignac, Eurenomics 2012-305608); by a Ruth L. Kirschstein NIH Service Award (to L.X. Xie, GM 007185); by Kids Kidney Research and Garfield Weston Foundation (to D. Böckenhauer and R. Kleta); by the King Abdul-Aziz University (to J.A. Kari, D. Böckenhauer, and R. Kleta); by the Fondazione CARIPARO (to L. Salviati); by a National Science Foundation grant (to C.F. Clarke, 0919609); and by the German Network of mitochondrial disorders (to H. Prokisch, mitoNET 01GM1113C). The LC-MS/MS determination of quinones was supported in part by NIH grant S10RR024605 from the National Center for Research Resources. The authors also acknowledge with thanks the Deanship of Scientific Research; King Abdulaziz University, Jeddah, for their support; the Bloomington stock center; and the Vienna Drosophila RNAi Center for Drosophila stocks. H.Y. Gee is a research fellow of the American Society of Nephrology. A.D. Paterson holds a Canada Research Chair in Complex Traits Genetics. W. Zhou is a Carl W. Gottschalk Scholar. D. Böckenhauer is a Higher Education Funding Council for England Clinical Reader. D.S. Williams is an Research to Prevent Blindness Jules and Doris Stein professor. F. Hildebrandt is an investigator of the Howard Hughes Medical Institute and the Frederick G.L. Huetwell Professor.
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