Abstract
Acrokeratoelastoidosis (AKE) is a rare autosomal dominant hereditary skin disease characterized by small, round-oval, flat-topped keratotic papules on the palms, soles and dorsal aspect of hands or feet. The causative gene for AKE remains unidentified. This study aims to identify the causative gene of AKE and explore the underlying biological mechanisms. A large, three-generation Chinese family exhibiting classic AKE symptoms was identified. A genome-wide linkage analysis and whole-exome sequencing were employed to determine the causative gene. shRNA knockdown in human skin fibroblasts and CRISPR/Cas9 knockout in HEK293T cells were utilized to assess gene functions in the progression of elastic fiber biosynthesis. The linkage analysis identified a susceptibility region between rs7296765 to rs10784618 on chromosome 12. Whole-exome sequencing confirmed a splicing mutation of 1101 + 1 G > A in the CCDC91 gene, resulting in exon 11 skipping and a subsequent 59-amino-acid-residue loss (residues L309-Q367del). Further functional analysis revealed distended Golgi cisternae, cytoplasmic vesicle accumulation, and lysosome presence. Immnunostaining of si-CCDC91-HSF cells demonstrated tropoelastin accumulation in the Golgi and abnormal extracellular aggregates. There are no significant changes in Fibrillin-1 microfibril assembly and lysyl oxidase activity. The findings strongly suggest that the protein product of the CCDC91 gene plays a crucial role in elastin transport. This discovery enhances our understanding of CCDC91’s function and broadens the known pathogenic mechanisms of AKE.
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Introduction
Acrokeratoelastoidosis (AKE) (OMIM:101850) is an autosomal dominant hereditary skin disorder characterized by bilateral multiple hyperkeratotic papules primarily distributed on the lateral portion of the palmoplantar regions. It was initially described by Oswaldo Costa in 1953 [1, 2]. Clinically, the first lesions typically develop during childhood or early adulthood and progressively increase in size and number, eventually becoming grouped or forming plaques [3, 4].
The primary etiology of AKE remains elusive. Both sporadic and familial cases of autosomal dominant inheritance have been reported in the literature. Previous studies have suggested that light exposure and trauma may constitute risk factors for sporadic cases [5]. In 1983, Greiner et al. demonstrated a potential linkage to chromosome 2 based on genetic mapping of 21 affected members [6]. Although AKE was classified as type III punctate palmoplantar keratoderma (PPKP3) in 1996 [7], some pathogenesis elements of palmoplantar keratoderma, such as the AAGAB gene in type I palmoplantar keratoderma (PPKP1), have been found not to be involved in AKE [8]. Consequently, current research still has not identified the pathogenic gene of AKE.
In this study, we report the identification of a splicing mutation in the CCDC91 gene (OMIM: 617366) within a Chinese family affected by AKE. Further functional analysis suggests that this gene may influence vesicle transport within the Golgi apparatus, thereby interfering with the synthesis and secretion of elastin.
Materials and methods
Subjects and clinical characteristics
In this study, we recruited a three-generation AKE family from Jiangsu province, China, consisting of 22 living individuals, including ten males and twelve females. (Fig. 1a). All patients were diagnosed by experienced clinical dermatologists at the Shanghai Skin Disease Hospital based on typical clinical manifestations and histological features. The proband (III-7), a 28-year-old man, presented an 18-year history of multiple keratotic papules on his hands. The first small asymptomatic papule developed on his right hand and gradually increased in number. Further physical examination revealed multiple, flesh-colored, shiny papules symmetrically present along the margins of both hands, resembling a “paving stone” appearance (Fig. 1b, c). After immersion for 5 min, the rash on the palms and back of the hands became swollen and whitish (Fig. 1d, e). None of the patients had a history of hyperhidrosis, trauma, or excessive sun exposure. A skin-biopsy specimen from a papule, collected from the proband via skin biopsies, was stained with traditional hematoxylin and eosin (H&E) stain and Verhoeff-Van Gieson (VVG) stain. Histological examination revealed thick hyperkeratosis within focal cup-like depressions of the epidermis, hypergranulosis, slight acanthosis, and sparse perivascular lymphocytic infiltration in the superficial dermis (Fig. 1f). VVG stain revealed thick, curved, coarse, fragmented, and rarefied elastic fibers in the reticular dermis (Fig. 1g).
DNA Isolation
Following informed consent, peripheral venous blood samples were collected from the proband and his family members. Genomic DNA was extracted from peripheral blood using the QIAamp DNA Blood Mini Kit (catalog number 51304, Qiagen, Valencia, CA, USA). The concentration and purity of the DNA were assessed utilizing a NanoDrop2000 Spectrophotometer (Thermo Scientific, Waltham, USA).
Genotyping and linkage analysis
A comprehensive genome-wide SNP genotyping was executed employing the Illumina Human 660W-Quad_v1 BeadChips (Illumina, San Diego, CA), encompassing 655,214 SNP and copy number variation (CNV) probes. Ultimately, 6,886 markers were examined through multipoint parametric linkage analysis using the MERLIN program (version 1.1.2; Ann Arbor, MI, USA).
Whole-exome sequencing
A total of 1 µg of DNA from the proband and three family members was employed to generate genomic DNA libraries, adhering to the protocols recommended by Illumina. Subsequently, Roche NimbleGen’s SeqCap EZ Human Exome Library v3.0 (64 Mb) was utilized for capture the genome’s exon regions. Following capture and PCR amplification, the libraries underwent sequencing via Illumina Hiseq 2000 Analyzers (Illumina, San Diego, USA). The remaining reads were aligned to the standard human genome reference (hg19) using Burrows-Wheeler analysis with default parameters [9]. Variants were sequentially filtered against dbSNP138, the 1000 Genomes project, and Hapmap 8.
Sanger sequencing validation
All potential mutations identified through next-generation sequencing (NGS) were further confirmed via Sanger sequencing. The primer sequences are provided in Table S1. The PCR products were purified using the TIANgel Midi Purification Kit (TianGen, Beijing, China). The purified PCR products were examined with the 3730xl Capillary Sequencer (Applied Biosystems). Sequence comparisons and analyses were conducted using DNASTAR software.
Reverse transcription-polymerase chain reaction (RT-PCR)
Peripheral blood mononuclear cells (PBMCs) were isolated via Ficoll-Uromiro cell density centrifugation. Subsequently, total RNA from the PBMCs was extracted using TRIzol Reagent (Invitrogen). Design primers around the splicing site (Table S1)and synthesize cDNA using the PPrimeScriptTMII 1st Strand cDNA Synthesis Kit (TaKaRa Bio Inc, Tokyo, Japan). Finally, the PCR products of the proband and healthy individuals were sequenced.
Cell culture
Human skin fibroblasts (HSF) were obtained from the Laboratory of Cell Biology at the Second Military Medical University (Shanghai, China). Cells were cultured in high-glucose Dulbecco’s Modified Eagle’s Medium (DMEM, Gibco) supplemented with 10% fetal bovine serum (FBS, BI) and 100 units of penicillin-streptomycin (Hyclone). Human embryonic kidney (HEK) 293 T cells were cultivated in the same medium with the addition of 10% FBS. All cell lines were maintained at 37 °C in a humidified atmosphere containing 5% CO2.
Knockdown of CCDC91 gene in HSF
Four distinct short hairpin RNA (shRNA) sequences were designed based on the CCDC91 reference sequence (Gene Bank Accession No. NM_018318.5) using online siRNA tools (Table S1). The target sequences were synthesized and cloned into an over-expressing lentiviral vector. All specific shRNAs were verified through sequencing.
The vectors were transfected into 293 T cells to generate packaged lentivirus, which was subsequently screened by adding 3 µg /ml puromycin. After determining the virus titer, the lentiviral stock was transfected into the HSF cell line. To assess the interference effect, CCDC91 expression was detected using quantitative real-time PCR (Q-PCR) and western blot techniques. Q-PCR was performed using SYBR Premix Ex TaqTM II (Takara Bio Inc., Tokyo, Japan) on a LightCycler 480 real-time platform (Roche, Basel, Switzerland). The primers are presented in Table S1, and GAPDH was measured as the house-keeping gene.
CRISPR/Cas9 knockout of exon 11 in HEK293T
Based on the CCDC91 gene sequence, two guide RNAs were designed to target exon 11 (Table S1). The sequences were validated using the CRISPR design tool (http://crispr.mit.edu/) and cloned into pSpCas9-2A-Puro (PX459) employing the BbsI enzyme (Thermo Fisher Scientific). The plasmid was cloned into Escherichia coli (DH5a) and subsequently extracted using a Miniprep kit (Qiagen).
HEK293T cells were transfected using Lipofectamine 2000 (Thermo Fisher Scientific). Following 8 h of transfection, cells were cultured in complete, fresh DMEM medium and screened by adding 3 µg /ml puromycin. Finally, the cDNA of the CCDC91 gene was sequenced to evaluate the knockout effect.
Immunofluorescence analysis
To investigate the function of CCDC91, we assessed the structural impairment of the Golgi apparatus by performing immunofluorescence analysis in HSF cells with low CCDC91 expression and HEK293T cell which was knockout CCDC91 exon 11. Cells grown on glass coverslips were fixed in 4% formaldehyde for 10 min. After washing with PBS, cells were blocked for 30 min in 1% BSA, and subsequently incubated with primary antibodies against human CCDC91 (sc-514452, Santa Cruz) and GM130 (12480 T, Cell Signaling Technology) at 4 °C overnight. Different secondary antibodies were used for the two cell lines, anti-mouse IgG Alexa Fluor 488 (Invitrogen) and anti-rabbit IgG Alexa Fluor 568CyTM3 (Invitrogen) in HSF and anti-mouse (IgG Alexa Fluor 488 CST) and anti-rabbit IgG Alexa Fluor 594CyTM3 (CST) in HEK293T. DNA was stained by DAPI. Images were acquired and analyzed using laser scanning microscopy (LSM880, Carl Zeiss, Germany).
Furthermore, to investigate the influences of CCDC91 gene on elastic fiber, the expression and distribution of the human recombinant tropoelastin (TE), human aortic alpha elastin, and human fibrilin-1 were evaluated using immunofluorescence analysis in HSF cells with low CCDC91 expression. against TE (PR398, Elastin Products Company, Owensville, MO, USA), human aortic alpha elastin (PR533, EPC), human fibrilin-1 (NBP1-84722, NOVUS biologicals).
Transmission electron microscope (TEM)
Cultured HSF and HEK293T cells were harvested and fixed in 0.1 mol/L phosphate buffer containing 2.5% glutaraldehyde at 4 °C overnight. Cells were then washed and post-fixed in 1% OsO4 buffer for 1 h at 4 °C. Following dehydration in a graded ethanol series, the samples were infiltrated with a Spurr resin and propylene oxide mixture for 24 h at room temperature. Finally, the samples were embedded in Spurr resin. Ultrathin sections were prepared using an EM UC6 ultra-microtome (Leica, Wetzlar, Germany) and stained with 3% uranium acetate and lead citrate at room temperature for 10 min. The samples were observed and imaged using a transmission electron microscope (JEM-1230, Japan) operating at 120 kV.
Enzyme-linked immunosorbent assay (ELISA)
Culture medium was collected from fibroblasts after 10 days cultures. Insoluble elastin was quantified using the Human Elastin SimpleStep ELISA kit (ab239433) following the manufacturer’s instructions.
Statistical and bioinformatics analysis
Results are presented as mean ± standard deviation (SD). Differences among groups were assessed using one-way ANOVA, with a p-value of less than 0.05 considered statistically significant. The three-dimensional structure model of the CCDC91 protein was generated using a combination of software applications, including FR-t5-M [10, 11] and I-TASSER [12]. The wild-type and mutant forms of CCDC91 were optimized using the side-chain packing program CIS-RR [13]. The structure models were visualized using PyMOL software (www.pymol.org/). Additionally, the impact of the deletion mutation(L309_Q367del) in CCDC91 was evaluated using the PROVEAN [14].
Results
Linkage analysis of the AKE Family
Owing to the current lack of reports on the genetic causes of AKE, we conducted genotype analysis on 17 individuals from this AKE family. Linkage analysis revealed chromosome 12 (46.93–56.50 cM), located between rs7296765 to rs10784618, as the susceptibility region due to the shared common haplotype among all affected individuals (Fig. 2a). The maximal LOD score was 3.55 (Fig. 2b, Table S3).
Whole exome sequencing identified CCDC91 mutations
We performed whole exome sequencing (WES) on four individuals from this family (Fig. 1a). We identified eight possible variants that appeared to be pathogenic (Table S2), and only the CCDC91 gene located in the susceptibility region identified in the linkage analysis (Fig. 2c).
Further validation with Sanger sequencing confirmed a heterozygous splice mutation in CCDC91(NM_018318: exon11: c.1101+1 G > A), which was present in the affected individuals, but absent in unaffected individuals (Fig. 2d).
To determine the function of splicing mutations (c.1101+1 G > A), primers were designed in the mutation site area for RT-PCR. The results of electrophoresis showed that the healthy individual had only one cDNA fragment (606 bp), while patients exhibited two bands (606 bp and 429 bp) (Fig. 2e), suggesting that an abnormal cDNA fragment was generated by alternative splicing in CCDC91. Further Sanger sequencing indicated that c.1101+1 G > A mutation could result in the deletion of exon11 from mature RNA (Fig. 2f), which caused a 59-amino-acid-residue loss in the ccdc91 protein (residues L309-Q367del).
Bioinformatics prediction of structural changes in alternative splicing transcript
Due to the exon deletion observed in exon 11 of CCDC91, we assessed the evolutionary conservation of the missing amino acid residues and discovered that they were highly conserved among mammalian species (Fig. 2g). Further structural analysis revealed that the lost residues (L309_Q367del) form a stable motif comprising two alpha-helices opposing antiparallel beta-sheets (Fig. 2h). In comparison to the wild-type ccdc91 protein (Fig. 2i), the mutant protein exhibits a narrower structure and a more concave surface, which may significantly impact its function (Fig. 2j). This result is also supported by the PROVEAN prediction of the deletion mutation (L309_Q367del), which is deleterious (−115.041).
Abnormal Golgi apparatus in ccdc91 knockdown of HSF and Exon 11 knockout in HEK293T
To investigate whether the CCDC91 gene affects the AKE phenotype, we introduced packaged shRNA-encoding lentivirus into HSF cells. A successful knockdown of ccdc91 expression was observed via QPCR and Western blot (Fig. 3a, b). Considering that ccdc91 is located in the Golgi apparatus, which is essential for elastin transportation, we performed immunofluorescence staining to detect ccdc91 and Golgi marker GM130. As shown in Fig. 3c and 3d, significant co-localization of overlapping signals from GM130 (red) and ccdc91 (green) was observed in both groups. Furthermore, we observed a dispersed, vesicular morphology of the Golgi apparatus in CCDC91 knockdown cells compared to the negative control (Fig. 3f). Additional TEM analysis revealed that, compared to the negative control (Fig. 3e, g), the Golgi apparatus in the CCDC91 knockdown group appeared more swollen and fragmented into numerous small pieces, suggesting that reduced CCDC91 expression may lead to elastin transport disorder, causing its accumulation in the Golgi apparatus. Additionally, increased lysosomes and autophagosomes were observed in this group (Fig. 3f, h).
As the c.1101+1 G > A mutation results in the loss of exon 11 in the CCDC91 gene, we employed the CRISPR/CAS9 system to knock out exon 11 in 293 T cell line (Fig. S1a, S1b). Compared to the negative control, we observed significant swelling of the Golgi apparatus in the CRISPR-CCDC91 293 T cell line (Fig. S1e, S1f).
Abnormal tropoelastin deposition in CCDC91 knockdown of HSF
Given that AKE is characterized by abnormal structure or quantities of elastic fibers, and tropoelastin, elastin, and fibrillin microfibril are essential components for elastic fiber biosynthesis. Compared to control the normal control group, Immunostaining for insoluble elastin revealed a reduction in si-CCDC91-HSF (Fig. 4c, d). An increased immunoreactivity from globular TE deposits was identified in si-CCDC91-HSF (Fig. 4a, b). No significant differences in fibrillin-1 were observed between si-CCDC91-HSF and the control fibroblasts (Fig. 4e, f). These results further suggested that CCDC91 may affect the structure of elastic fibers by interfering with elastin transport, while not impacting fibrillin-1. A subsequent quantitative assessment of insoluble elastin by ELISA demonstrated that the synthesis of insoluble elastin in si-CCDC91-HSF fibroblasts was significantly decreased compared to the control group (Fig. 4g).
Discussion
AKE is considered a hereditary skin disease with autosomal dominant transmission [15,16,17], although its genetic causes remain unclear. A genetic study involving 21 affected members has provided evidence for the genetic linkage of AKE to chromosome 2 [6]. Based on the histopathological characteristics of elastic fibers, one hypothesized pathogenesis may be related to a reduced number and impaired function of fibroblasts in the dermis [18]. A report has suggested that fragmented elastic fibres were not only observed in the lesional skin but also in normal-appearing, non-sun-exposed skin, indicating that the disorder could be considered a generalized defect of elastic tissue [4].
In the present study, we identified a novel splice mutation in the CCDC91 gene from a Chinese AKE family using linkage analysis and WES. Further Sanger sequencing revealed that the mutation was present in affected individuals but absent in unaffected individuals, confirming that the CCDC91 gene is one of the pathogenic genes of AKE.
The CCDC91 gene is located on the short arm of chromosome 12 (12p11.22). It has 13 exons, with the first three exons subject to alternative splicing [19]. Although the splicing is highly variable at the 5-prime exons, other exons are conserved, encoding a protein composed of 441 amino acids with a predicted central coiled-coil domain. Immunofluorescence analysis demonstrated that ccdc91 colocalized with GGA1, GGA2, and GGA3, which is a critical accessory protein that promotes transport of carrier vesicles between the Golgi and lysosomes [20]. Although the function of ccdc91 is not well understood, some genome-wide association studies (GWAS) studies have reported that CCDC91 polymorphism may be associated with lung function and ossification of the posterior longitudinal ligament [21, 22]. A meta-analysis of 17 GWAS studies identified sentinel variants in or near the CCDC91 gene associated with forced vital capacity (FVC), a key criterion for the diagnosing restrictive lung diseases such as pulmonary fibrosis [21]. Further expression analysis indicated that the CCDC91 gene was over-expressed in lung tissue and was relevant to lung function in a DNase-seq experiment. These results suggest that the CCDC91 gene may be an important regulator of elastic fiber homeostasis.
Previous studies have suggested that keratotic papules may be caused by over-production of filaggrin [23, 24]. while disturbances in elastic fiber have been observed in some AKE cases [25]. Elastin, the most abundant protein in elastic fibres, constitutes nearly 90% of the mature structure [26]. It is encoded by the ELN gene and initially synthesized as a soluble precursor tropoelastin (TE) polypeptide on the ribosome. Following synthesis, the secreted TE polypeptide is transported to the endoplasmic reticulum for preliminary processing and then to the Golgi apparatus for further modification [27]. Finally, soluble TE is secreted from the Golgi apparatus into the extracellular matrix, where it aggregates to form spherical elastin [28, 29]. During this assembly process, the CCDC91 gene, located in the Golgi, may experience mutations that interfere with tropoelastin transport, leading to tropoelastin accumulation within the Golgi and significantly reduced deposition of mature elastin. In this study, we utilized a CCDC91 knockdown cell line and a 293 T cell with exon 11 of CCDC91 knockout, observing a significant swelling of the Golgi apparatus, increased lysosomes, and accumulation of vesicles in the cytoplasm. These findings further support our hypothesis that CCDC91 gene mutations may affect vesicle transport within the Golgi apparatus and limit the synthesis and secretion of elastin.
Clinically, AKE is characterized by multiple, firm, round-to-oval, flesh-colored or yellowish keratotic papules along the lateral or medial borders of hands or feet, typically distributed in a bilateral and symmetrical pattern. However, some unilateral cases have been reported [30,31,32], which have been attributed to genetic mosaicism. In this study, we observed multiple, flesh-colored, shiny papules along the margins of both hands in affected individuals, suggesting that the pathogenic mutation may have originated from germline cells. After immersing the hands for five minutes, lesions appeared swollen and whitish. Similar clinical phenotypes have been described in aquagenic palmoplantar keratoderma (APK), characterized by translucent or whitish papules on the palms and soles that develop after brief water exposure [33, 34]. Although several studies have linked APK with cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction [35, 36], we did not identify any CFTR gene mutations in our study. Interestingly, a previous report described a patient with concurrent AKE and APK appearing, yet without CFTR gene mutations [37]. These findings further suggest that AKE pathogenesis may differ from APK, and the thick hyperkeratosis induced by AKE potentially altering ion or protein channels of the eccrine ducts.
Although familial and sporadic AKE have been reported, the underlying pathogenic genes of AKE are still unknown. Our probands and their affected family members exhibit characteristic clinical and histological features of AKE. In this study, we also collected two sporadic cases and detected the causative gene by NGS. However, we did not find any genetic variants in the CCDC91 (Table S4). Therefore, we inferred that the pathogenic mechanism of hereditary AKE may be different from sporadic cases. Further genetic studies are warranted to test this speculation.
In summary, we investigated a Chinese family presenting with characteristic AKE lesions on the palms, soles and dorsal aspect of hands or feet. Through linkage analysis and deep sequencing, we identified a causative mutation in the CCDC91 gene. Our study further suggests that the ccdc91 protein may function as a regulator, enhancing the vesicular transport of elastin from the Golgi apparatus to the extracellular matrix. Its dysfunction may lead to abnormalities in elastic fibers, potentially contributing to the typical lesions observed in AKE patients.
Data availability
The datasets generated during the current study are available from the corresponding author.
References
Costa OG. Akrokerato-elastoidosis; a hitherto undescribed skin disease. Dermatologica. 1953;107:164–8.
Costa OG. Acrokeratoelastoidosis. AMA Arch Derm Syphilol. 1954;70:228–31.
Bogle MA, Hwang LY, Tschen JA. Acrokeratoelastoidosis. J Am Acad Dermatol. 2002;47:448–51.
Fiallo P, Pesce C, Brusasco A, Nunzi E. Acrokeratoelastoidosis of costa: a primary disease of the elastic tissue? J Cutan Pathol. 1998;25:580–2.
Highet AS, Rook A, Anderson JR. Acrokeratoelastoidosis. Br J Dermatol. 1982;106:337–44.
Greiner J, Kruger J, Palden L, Jung EG, Vogel F. A linkage study of acrokeratoelastoidosis. Possible mapping to chromosome 2. Hum Genet. 1983;63:222–7.
Stevens HP, Kelsell DP, Bryant SP, Bishop DT, Spurr NK, Weissenbach J, et al. Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas. Arch Dermatol. 1996;132:640–51.
Taki T, Ogawa Y, Sakakibara A, Kono M, Akiyama M. Image gallery: unilaterally dominant acrokeratoelastoidosis (punctate palmoplantar keratoderma type 3). Br J Dermatol. 2017;177:e157.
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009;25:1754–60.
Dai W, Song T, Wang X, Jin X, Deng L, Wu A, et al. Improvement in low-homology template-based modeling by employing a model evaluation method with focus on topology. PLoS ONE. 2014;9:e89935.
Dai W, Wu A, Ma L, Li YX, Jiang T, Li YY. A novel index of protein-protein interface propensity improves interface residue recognition. BMC Syst Biol. 2016;10:112.
Yang J, Yan R, Roy A, Xu D, Poisson J, Zhang Y. The I-TASSER Suite: protein structure and function prediction. Nat Methods. 2015;12:7–8.
Cao Y, Song L, Miao Z, Hu Y, Tian L, Jiang T. Improved side-chain modeling by coupling clash-detection guided iterative search with rotamer relaxation. Bioinformatics. 2011;27:785–90.
Choi Y, Sims GE, Murphy S, Miller JR, Chan AP. Predicting the functional effect of amino acid substitutions and indels. PLoS ONE. 2012;7:e46688.
Hussain A, Jenkins A, Feneran A, Abdulla F. New-onset acrokeratoelastoidosis in an immunosuppressed patient. JAAD Case Rep. 2018;4:75–76.
Xu CC, Fu LY, Lin D, Li H, Du WH, Wang PG. A case of acrokeratoelastoidosis. Clin Exp Dermatol. 2018;43:819–20.
Uribe P, Ortiz E, Wortsman X, Gonzalez S. Acrokeratoelastoidosis of the foot with clinical, dermoscopic, ultrasonographic, and histopathologic correlation. J Am Podiatr Med Assoc. 2018;108:178–81.
Zychowska M, Batycka-Baran A, Baran W. Acrokeratoelastoidosis as an example of marginal papular acrokeratoderma with prominent elastorrhexis. Postepy Dermatol Alergol. 2019;36:772–4.
Lui WW, Collins BM, Hirst J, Motley A, Millar C, Schu P, et al. Binding partners for the COOH-terminal appendage domains of the GGAs and gamma-adaptin. Mol Biol Cell. 2003;14:2385–98.
Mardones GA, Burgos PV, Brooks DA, Parkinson-Lawrence E, Mattera R, Bonifacino JS. The trans-Golgi network accessory protein p56 promotes long-range movement of GGA/clathrin-containing transport carriers and lysosomal enzyme sorting. Mol Biol Cell. 2007;18:3486–501.
Soler Artigas M, Wain LV, Miller S, Kheirallah AK, Huffman JE, Ntalla I, et al. Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Nat Commun. 2015;6:8658.
Nakajima M, Takahashi A, Tsuji T, et al. A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine. Nat Genet. 2014;46:1012–6.
Abulafia J, Vignale RA. Degenerative collagenous plaques of the hands and acrokeratoelastoidosis: pathogenesis and relationship with knuckle pads. Int J Dermatol. 2000;39:424–32.
Pfendner EG, Vanakker OM, Terry SF, Vourthis S, McAndrew PE, McClain MR, et al. Mutation detection in the ABCC6 gene and genotype-phenotype analysis in a large international case series affected by pseudoxanthoma elasticum. J Med Genet. 2007;44:621–8.
Johansson EA, Kariniemi AL, Niemi KM. Palmoplantar keratoderma of punctate type: acrokeratoelastoidosis Costa. Acta Derm Venereol. 1980;60:149–53.
Baldwin AK, Simpson A, Steer R, Cain SA, Kielty CM. Elastic fibres in health and disease. Expert Rev Mol Med. 2013;15:e8.
Chung MI, Miao M, Stahl RJ, Chan E, Parkinson J, Keeley FW. Sequences and domain structures of mammalian, avian, amphibian and teleost tropoelastins: Clues to the evolutionary history of elastins. Matrix Biol. 2006;25:492–504.
Muiznieks LD, Cirulis JT, van der Horst A, Reinhardt DP, Wuite GJ, Pomès R, et al. Modulated growth, stability and interactions of liquid-like coacervate assemblies of elastin. Matrix Biol. 2014;36:39–50.
Hinek A, Pshezhetsky AV, von Itzstein M, Starcher B. Lysosomal sialidase (neuraminidase-1) is targeted to the cell surface in a multiprotein complex that facilitates elastic fiber assembly. J Biol Chem. 2006;281:3698–710.
AlKahtani HS, AlHumidi AA, Al-Hargan AH, Al-Sayed AA. A sporadic case of unilateral acrokeratoelastoidosis in Saudi Arabia: a case report. J Med Case Rep. 2014;8:143.
Klekowski N, Shwayder T. Unilateral acrokeratoelastoidosis-second reported case. Pediatr Dermatol. 2011;28:20–22.
Moulin C, Petiot-Roland A, Chouvet B, Faure M, Claudy A. [Unilateral acro-keratoelastoidosis]. Ann Dermatol Venereol. 1996;123:654–6.
Cabrol C, Bienvenu T, Ruaud L, Girodon E, Noacco G, Delobeau M, et al. Aquagenic palmoplantar keratoderma as a CFTR-related disorder. Acta Derm Venereol. 2016;96:848–9.
D’Erme AM, Braggion C, de Martino M, Greco A. Aquagenic palmoplantar keratoderma: a sign of cystic fibrosis early in life. Int J Dermatol. 2014;53:e536–8.
Raynal C, Girodon E, Audrezet MP, Cabet F, Pagin A, Reboul MP, et al. CFTR gene variants: a predisposition factor to aquagenic palmoplantar keratoderma. Br J Dermatol. 2019;181:1097–9.
Denos C, Dreyfus I, Chiaverini C, Labreze C, Abasq C, Phan A, et al. [Clinical and evolutionary characteristics of a child with aquagenic keratoderma: a retrospective study of 12 patients]. Ann Dermatol Venereol. 2018;145:250–6.
Poiraud C, Vourc’h-Jourdain M, Cassagnau E, Barbarot S. Aquagenic palmoplantar keratoderma associated with acrokeratoelastoidosis. Clin Exp Dermatol. 2014;39:671–2.
Acknowledgements
We are grateful to the patients for their interest and participation in this study.
Funding
This work was supported by the Key Project of Clinical Research from Shanghai Hospital Development Center (SHDC2020CR4020; SHDC12020117) and Funding from Shanghai Skin Disease Hospital (2018KYQD01). We are grateful to the patients for their interest and participation in this study.
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YL and YB coordinated the project. WN and FW participated in the blood sample preparation and DNA extraction. YLand YB directed and performed NGS and SNP microarray. YL and WN were responsible for cell culture and construction. FW, MY and NH were responsible for immunostaining, transmission electron microscope and ELISA. YL, YB and ML performed the data analyses and wrote the manuscript. YB perform the analysis with NGS data.
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All clinical details and images have been obtained with the patient’s informed consent. This study has been approved by the Ethics Committee of Shanghai Dermatology Hospital.
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Zhu, Y., Bai, Y., Yan, W. et al. A mutation in CCDC91, Homo sapiens coiled-coil domain containing 91 protein, cause autosomal-dominant acrokeratoelastoidosis. Eur J Hum Genet (2024). https://doi.org/10.1038/s41431-024-01573-3
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DOI: https://doi.org/10.1038/s41431-024-01573-3