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. 2018 Jan 22;41(1):1–8. doi: 10.1590/1678-4685-GMB-2016-0162

Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation

Asmat Ullah 1,*, Ajab Gul 2,*, Muhammad Umair 1, Irfanullah 1, Farooq Ahmad 1, Abdul Aziz 3, Abdul Wali 2, Wasim Ahmad 1
PMCID: PMC5901503  PMID: 29384555

Abstract

Split-hand/split-foot malformation (SHFM), also known as ectrodactyly is a rare genetic disorder. It is a clinically and genetically heterogeneous group of limb malformations characterized by absence/hypoplasia and/or median cleft of hands and/or feet. To date, seven genes underlying SHFM have been identified. This study described four consanguineous families (A-D) segregating SHFM in an autosomal recessive manner. Linkage in the families was established to chromosome 12p11.1–q13.13 harboring WNT10B gene. Sequence analysis identified a novel homozygous nonsense variant (p.Gln154*) in exon 4 of the WNT10B gene in two families (A and B). In the other two families (C and D), a previously reported variant (c.300_306dupAGGGCGG; p.Leu103Argfs*53) was detected. This study further expands the spectrum of the sequence variants reported in the WNT10B gene, which result in the split hand/foot malformation.

Keywords: Split-Hand-Foot Malformation 6, WNT10B gene, sequence variants

Introduction

Split-hand/split-foot malformation (SHFM) is a congenital limb defect characterized by absence of medial digital rays, median clefts of the hands and feet, aplasia and/or hypoplasia of the phalanges, and syndactyly (McKusick, 1998; Duijf et al., 2003). In severe cases, feet exhibit a lobster claw-like appearance with a deep median groove. Asymmetric manifestations, variable syndactyly and nonpenetrance of the disorder have also been described (Ozen et al., 1999). Few SHFM patients have been found with signs of intellectual disability, ectodermal and craniofacial defects, and orofacial clefting (Elliott and Evans, 2006). Clinical features of SHFM vary from patient to patient and within the same individual (Duijf et al., 2003; Elliott and Evans 2008; Sowinska-Seidler et al., 2014). Both isolated (non-syndromic) and syndromic forms of SHFM have been reported in the literature.

Seven types of non-syndromic SHFM have been mapped on different human chromosomes. Four of these forms (SHFM-1, SHFM-3, SHFM-4, SHFM-5) inherit in autosomal dominant pattern, SHFM-2 in X-linked inherited, and SHFM-6 in autosomal recessive pattern. The four autosomal dominant forms were mapped on chromosome 7q21 (SHFM-1; MIM183600) (Scherer et al., 1994), 10q24 (SHFM-3; MIM246560) (Nunes et al., 1995; Gurrieri et al., 1996; Raas-Rothschild et al., 1996), 3q27 (SHFM-4; MIM605289) (Ianakiev et al., 2000) and 2q31 (SHFM-5; MIM606708) (Boles et al., 1995). The autosomal recessive form (SHFM-6; MIM 225300) has been mapped on chromosome 12q13.11-q13 (Ugur and Tolun, 2008). The X-linked form was mapped on Xq26, which was later refined to a small region of 5.0 cM (Faiyaz-Ul-Haque et al., 2005). Based on genome-wide linkage analysis in a single family with autosomal recessive inheritance pattern, Gurnett et al. (2006) mapped a novel locus for SHFM on chromosome 8q21.11–q22.3. For these seven loci, only three (SHFM1, SHFM4, SHFM6) have been solved at the gene level. A causative gene of the wingless-type MMTV integration site family, member 10 (WNT10B, MIM 601906) has been reported of causing SHFM-6 (Ugur and Tolun, 2008). Ianakiev et al. (2000) reported the gene TP63 (tumor protein p63, MIM 603273), which encodes a homolog of the tumor suppressor responsible for the SHFM-4 phenotype. Shamseldin et al. (2012) reported a mutation in the gene DLX5 responsible for the SHFM-1 phenotype in a consanguineous family. We reported intragenic variants in the DLX5 and DLX6 genes that caused the SHFM-1 phenotype in two different families (Ullah et al., 2016a,b). Goodman et al. (2002) proposed that SHFM-5 and other digit defects may be caused by haploinsufficiency of genes (EVX2, DLX1, DLX2) located at the 5′ end of the HOXD cluster. Recently, Umair et al. (2017) reported a homozygous variant in the EPS15L1 gene located on chromosome 19p13.11 causing isolated SHFM in a Pakistani family.

In this study, we investigated four consanguineous families of Pakistani origin showing split hand and foot malformation phenotypes. Linkage in the families was established to SHFM6 on chromosome 12p11.1-q13.13. Sequence analysis of the WNT10B gene detected a novel nonsense and a previously reported variant in affected individuals.

Materials and Methods

Family history

Approval to conduct the study was obtained from the Institutional Review Board (IRB) of Quaid-i-Azam University, Islamabad Pakistan. Four consanguineous families with clinical manifestations of split hand and foot malformations (SHFM were recruited from remote areas of Pakistan. Pedigree reconstruction (Figure 1) provided convincing evidence of an autosomal recessive mode of inheritance of the disorder. Six individuals with SHFM were identified in four families. This included a male (IV-1) and a female (IV-2) in family A, a female (IV-1) in the fourth generation in family B, two males (IV-2, IV-3) in the fourth generation in family C, and one male (V-1) in the fifth generation in family D. All affected and unaffected individuals in the four families were examined by medical specialists at local government hospitals. Blood samples were collected from both affected and unaffected individuals of the families after obtaining written consent.

Figure 1. Haplotypes constructed in families (A to D) segregating SHFM6. Black symbols represent affected individuals while clear symbols represent unaffected individuals. The shaded black alleles are forming risk haplotype, while the alleles shown in white are not co-segregating with the disease. Genetic distances in centi-Morgans (cM) are according to the Rutgers combined linkage-physical map (Build 36.2).

Figure 1

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Isolation of Genomic DNA

Peripheral blood samples were obtained from 19 individuals in EDTA containing vacutainer sets (BD, Franklin Lakes, NJ, USA). Genomic DNA extraction was performed using a standard phenol-chloroform procedure. DNA was quantified using a Nanodrop-1000 spectrophotometer (Thermal Scientific, Wilmington, MA).

Genotyping

Linkage in the families was searched by genotyping microsatellite markers mapped in the flanking regions of autosomal dominant and autosomal recessive forms of SHFM. This included SHFM1 (D7S2537, D7S2481, D7S630, D7S492, D7S627, D7S1813, D7S657, D7S527, D7S479) at chromosome 7q21, SHFM3 (D10S520, D10S91, D10S1736, D10S1726, D10S603, D10S1710, D10S383, D10S1264) at chromosome 10q24, SHFM4 (D3S3570, D3S3600, D3S3596, D3S1661, D3S2747, D3S1662, D3S2311, D3S1305) at chromosome 3q27, SHFM5 (D2S124, D2S2345, D2S294, D2S2302, D2S1274, D2S2257, D2S2173, D2S2978) at chromosome 2q31, SHFM6 (D12S1034, D12S823, D12S1042, D12S1337, D12S1698, D12S87, D12S1584, D12S1621, D12S291, D12S1301, D12S1713, D12S1701, D12S339, D12S1590, D12S1620, D12S1635, D12S347, D12S297, D12S368, D12S398, D12S1604, D12S325) at chromosome 12q11-q13, and another SHFM locus mapped on chromosome 8q21.11–q22.3 (D8S526, D8S2321, D8S1119, D8S1818, D8S1129, D8S1714, D8S556) (Gurnett et al., 2006). PCR amplification of the microsatellite markers was performed as previously described (Ullah et al., 2015). The amplified PCR products were resolved on 8% non-denaturing polyacrylamide gels, stained with ethidium bromide, and genotypes were assigned by visual inspection. DNA ladders of 5, 10 and 20 bp (MBI Fermentas®, Life Sciences, York, UK) were used to determine allele size for respective microsatellite markers. Markers used in the genotyping were arranged according to Rutgers combined linkage-physical map (Build 36.2) of the human genome (Matise et al., 2007). Haplotypes were analyzed by SIMWALK2 (Sobel and Lange, 1996).

Sequencing of the WNT10B gene

Primers used for PCR amplification, sequencing and coding of intron-exon junctions of the WNT10B gene were the same as described earlier (Khan et al., 2012). The PCR-amplified products were purified with a commercially available kit (Axygen MD, USA) and sequenced using ABI BigDye Terminator Sequencing Kit v.3.1 (Applied Biosystems, Foster City, CA, USA). Sequence variants were identified via the BIOEDIT sequence alignment editor, version 6.0.7 (Ibis Biosciences, CA, USA).

In silico analysis

The pathogenicity index of the sequence variants identified here was calculated using the following softwares: Mutation Taster (http://www.mutationtaster.org/), Polymorphism Phenotyping V2 (PolyPhen-2) (http://genetics.bwh.harvard.edu/pph2/) and Sorting Intolerant From Tolerant (SIFT) (http://sift.bii.a-star.edu.sg/). The frequency of the variants in the general population was determined using the Exome Variant Server (EVS) (http://evs.gs.washington.edu/EVS/), and 1000 genomes.

Results

Clinical features

Affected individuals in the four families showed classical phenotypes of SHFM, which segregated in an autosomal recessive manner. At the time of the study, ages of the patients varied between 2 to 10 years. Patients were born after normal pregnancies. All the affected individuals showed cleft hand and cleft foot deformities associated with mesoaxial syndactyly (Figure 2).

Figure 2. Clinical features of split hand/foot malformation (SHFM) observed in family A. (a) Female patient (IV-1) showing cleft hand deformity with absence of middle finger in right hand, and syndactyly of 1st and 2nd finger. (b) Radiograph showing pre-axial syndactyly of index finger and thumb at distal phalanx as well as in 3rd and 4th metacarpals. (c, d) The same patient (IV-1) showing cleft hand deformity with central type syndactyly in her left hand, and with an additional bud on the 2nd metacarpal; distal phalanx in the middle finger is missing. (e, h) Classical cleft feet deformities characterized by central deficiency in the same affected individual, radiographs showing hallux valgus deformities in the big toe, missing central toes and presence of postaxial syndactyly in the metatarsal bones; some of the tarsal bones are missing. (i, j) Male affected individual (IV-2) showing cleft hand deformity associated with missing of 2nd and 3rd finger. (k, n) The same affected member showing cleft feet deformity; radiological study showing bilateral cleft hand/feet deformities associated with preaxial and postaxial syndactyly in the hands and feet, respectively. (o) Clinical features of an affected girl (IV-1) in family B showing missing big toe along with 2nd and 3rd toes. (p) An affected individual (IV-2) in family C showing absence of middle phalanx of 3rd finger in right hand, severe bilateral hypoplasia and fusion of the 3rd and 4th finger. (q, r) The same patient, showing pre-axial syndactyly in toes 1 and 2 in both feet, and an additional bud on the 3rd toe in right foot. (s) Radiographic features of the right hand of the patient (IV-2) showing radial ray malformation including hypoplasia of 1st metacarpal, complex fusion of middle finger to ring finger, relatively large proximal phalanx of 5th finger, fingers showing contractures and deviations. (t-u) Radiographs of the feet showing fusion of the 1st and 2nd toes. (v) Affected individual (IV-3) in family C showing bilateral cleft foot with missing 2nd and 3rd digits, central deficiency with rudimentary bud of lesser toe, classical cleft foot, and basal syndactyly formation. (w) Affected individual (V-1) in family D showing cleft foot deformity, i.e. longitudinal deficiency of digital ray of the foot except rays 1 or 5, central deficiency and varus deformity of lesser toe, claw toe deformity, classical cleft foot and fusion of the middle and distal phalanx of 5th toe.

Figure 2

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In family A, the affected female (IV-1) showed cleft hand deformity with absence of the middle finger in the right hand. Radiographs showed pre-axial syndactyly of the index finger and thumb at the distal phalanx as well as in the 3rd and 4th metacarpals (Figure 2a,b). The same patient showed cleft hand deformity with central syndactyly in her left hand with an additional bud on the 2nd metacarpal. The distal phalanx of the middle finger was also missing (Figure 2c,d). Classical cleft feet deformities, characterized by central deficiency, were present. Radiographs showed hallux valgus deformities of the big toe and missing central toes associated with postaxial syndactyly in the metatarsal bones. Some of the tarsal bones were absent (Figure 2e-h). The male individual of the same family (IV-2) showed the same SHFM phenotypes as the female (IV-1). Abnormalities such as syndactyly, radial ray malformation, dysplastic hands, and cleft feet were noted (Figure 2i-j). The radiological study revealed bilateral cleft hand/feet deformities associated with pre-axial and postaxial syndactyly in hands and feet, respectively (Figure 2k-n).

In family B, an affected girl (IV-1) was missing the big toe and toes 2 and 3 in the right foot. The left foot and the hands were apparently normal (Figure 2o).

One of the affected members (IV-2) of family C showed aplasia of the middle phalanx of the 3rd finger in the right hand, severe bilateral hypoplasia and fusion of the 3rd and 4th finger (Figure 2p). Fusion of the big toe and 2nd toe in both feet, and an additional rudimentary bud were observed in the 3rd toe of the right foot. Radial ray malformation including hypoplasia of the 1st metacarpal, as well as complex fusion of the middle and ring fingers. Fingers with contractures and deviations were observed in radiographs of the right hand of patient IV-2 (Figure 2q-u). The other affected member (IV-3) of family C showed bilateral cleft foot with missing 2nd and 3rd toes, characterized by central deficiency with rudimentary bud of lesser toe, classical cleft foot, and basal syndactyly formation (Figure 2v).

In family D, the affected person (V-1) showed cleft foot deformity, i.e. longitudinal deficiency of the digital ray of the foot except rays 1 and 5, central deficiency and varus deformity of the lesser toe, claw toe deformity, classical cleft foot and fusion of middle and distal phalanx of the 5th toe (Figure 2w). Abnormalities in skin, teeth, face, nails, and eyes were not observed in affected members of the four families. Parents of the affected people were normal and healthy.

Linkage and mutation analysis

Linkage in the families was tested by genotyping microsatellite markers. Haplotypes revealed that affected individuals were homozygous for markers linked to the WNT10B gene on chromosome 12q11-q13 (Figure 1). Subsequently, the WNT10B gene was sequenced in affected and unaffected members of the families. Sequence analysis detected a novel homozygous nonsense variant (c.460C > G, p.Gln154*) in exon 4 of the WNT10B gene in all the three affected members of the families A and B. In the two other families (C and D) a 7 bp duplication mutation (c.300_306dupAGGGCGG; p.Leu103Alafs*53) was detected in the affected members (Figure 3). The two sequence variants were present in heterozygous state in the obligate carriers in the families and were not identified in 150 ethnically matched control individuals. This absence and the available databases of genetic variations (ExAc, 1000 genome, EVS or dbSNP) confirm that these were not polymorphisms.

Figure 3. Sequence analysis of WNT10B gene showing a novel nonsense variant (c.460C > G, p.Gln154*) in affected individuals in family A and B. The upper panel (a) represents nucleotide sequences in an affected individual, the middle panel (b) in a heterozygous carrier and lower panel (c) in a normal individual; arrows indicate position of the sequence variant. (d) 7-bp duplication mutation (c.300_306dupAGGGCGG; L103Rfs*53) in the gene WNT10B found in affected individuals in family C and D, (e) in the heterozygous carrier, and (f) in an unaffected member of the family. Underline 7-bp sequence AGGGCGG is duplicated in affected members; arrows indicate position of duplication. (g, h) Leucine (L) amino acid represented in green is conserved across four different species. (i) Comparison of amino acid sequence of normal and mutated human WNT10B protein showing nonsense mutation (p.Gln154*) identified in family A and B. (j) Amino acid sequence comparison of normal and mutated human WNT10B protein showing substitution of leucine with arginine at amino acid position 103 and frame shift (Leu103Argfs*53). Comparison of amino acid sequence of human WNT10B protein with other orthologs.

Figure 3

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Discussion

To date, five sequence variants in the WNT10B gene causing SHFM have been reported. Clinical findings resulting from these variants are summarized in Table 1. Ugur and Tolun (2008) reported a large consanguineous family of Turkish origin in which affected individuals were homozygous for p.Arg332Trp in the WNT10B gene. Blattner et al. (2010) found a 4 bp duplication (c.458_461dupAGCA) in a Swiss woman affected with sporadic SHFM6. Previously, four families of Pakistani origin carrying variants in the WNT10B gene have been reported. This included a missense variant (p.Thr329Arg) (Khan et al., 2012), 4 bp deletion (c.1165_1168delAAGT), and 7 bp duplication (c.300_306dupAGGGCGG) (Aziz et al., 2014). A family reported by Khan et al. (2012) showed absence of fingers and thumbs, which were not observed in the families studied by Ugur and Tolun (2008) and Blattner et al. (2010).

Table 1. Comparison of the clinical features, due to sequence variants in the WNT10B gene, observed in participants of the present study and those reported previously.

Mutation Phenotypes Reference
p.Arg332Trp Syndactyly type I, postaxial partial syndactyly, flexion deformity of finger 2, Postaxial syndactyly (fingers 3–4) with almost fused nail beds, finger 5 clinodactyly, polydactyly type 1. Ugur and Tolun (2008)
p.Thr329Arg Syndactyly of radial ray and a rudimentary finger, pre-axial syndactyly of toe 1–2, post-axial syndactyly of toe 3–4 complex duplication of digit 3–4, Post-axial syndactyly of toe 3–4, absence of toe 2, digit 2 hypoplasia, agenesis of radial ray along with digit 1, pre-axial polydactyly type 1, Agenesis of distal ray at metacarpophalangeal joint level, fixed flexion contracture of both 4–5 digit at proximal interphalangeal joint level. Khan et al. (2012)
p.Lys388Glufs*36, p.Leu103Argfs*53 Central and pre- axial syndactyly, campodactyly, polydactyly, dysplastic (abnormal development) hands and cleft feet, hallux valgus deformity of big toe and rudimentary bud of lesser toes. Aziz et al. (2014)
p.Gln154* Mesoaxial type of syndactyly, pre-axial syndactyly of index finger and thumb at distal phalanx, cleft hand deformity with absence of middle finger, Aplasia of distal phalanx of the middle finger, hallux valgus deformities of big toe, missing central toes, missing of great thumb Present study
p.Leu103Argfs*53 Syndactyly of the great thumb and 2nd toe in feet and an additional rudimentary bud on 3rd toe, hypoplasia of 1st metacarpal, complex fusion of middle to ring finger, aplasia of middle phalanx of 3rd finger, bilateral hypoplasia and fusion of the 3rd and 4th finger, fingers with contractures and deviations, central deficiency and varus deformity of lesser toe, claw toe deformity. Present study
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In the present study, we have reported four additional Pakistani families with SHFM6 in autosomal recessive pattern. The SHFM features observed in affected members of the families included syndactyly, cleft hand/foot malformation, hallux valgus deformities, aplasia, hypoplasia, radial ray malformation, presence of extra rudimentary bone, hypoplastic finger and missing of phalanges. Features observed in affected members of the four families were similar to those reported previously (Ugur and Tolun, 2008; Khan et al., 2012; Aziz et al., 2014). However, polydactyly in few affected members of the families reported by Khan et al. (2012) and Aziz et al. (2014) were not observed in our study.

Microsatellite-based genotyping established linkage in the four families to SHFM6 on chromosome 12q11-q13, harboring the WNT10B gene. The gene WNT10B contains five exons spanning 6.5 kb of genomic DNA and gives rise to a 389 amino acids protein. WNT10B is a 45 kDa glycoprotein that plays a role in fetal limb bud development and adult hematopoiesis. Sequence analysis of the gene led to the identification of a novel nonsense variant (p.Gln154*) in two families (A and B) and a previously reported duplication (c.300_306dupAGGGCGG; p.Leu103Argfs*53) in the other families (C and D). The sequence variant (p.Gln154*) identified in family A and B is the first nonsense and sixth variant detected in the WNT10B gene. The premature stop codon at position 154 (p.Gln154*) results in a truncated transcript, which is probably degraded by nonsense mediated mRNA decay (Maquat, 1996, 2005). The 7 bp duplication (c.300_306dupAGGGCGG; Leu103Argfs*53) found in the other two families (C, D) changes the downstream nucleotide sequence, resulting in a premature stop codon (TGA). Thus, the mutant transcript produced is probably also degraded by nonsense-mediated mRNA decay.

The gene WNT10B belongs to the WNT gene family. Proteins encoded by the WNT gene family are involved in the activation of a canonical signaling pathway, acting as ligands for cell surface receptors complexes composed of frizzled (FZ) and low-density lipoprotein receptor-related protein 5/6 (LRP5/6) family members. Gordon and Nusse (2006) reported that binding of WNT to FZ and LRP5/6 results in the disruption of the APC/Axin/GSK3 complex that is required for the targeted degradation of β-catenin.

In conclusion, we have reported a novel and a previously known sequence variant in the WNT10B gene in four consanguineous families affected by SHFM. This further extended the spectrum of mutations in the WNT10B gene that result in split hand/foot malformation. These findings can improve diagnosis and genetic counseling, and form the basis of prenatal testing.

Acknowledgments

We are highly indebted to the family members for their invaluable cooperation and participation in this study. Muhammad Umair was supported by HEC Indigenous Ph.D. Fellowship.

Footnotes

Associate Editor: Maria Rita Passos-Bueno

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