A new family with spastic paraplegia type 51 and novel mutations in AP4E1

Background Autosomal recessive mutations in the AP-4 (adaptor protein complex 4) complex subunit ϵ − 1 (AP-4E1) gene on chromosome 15q21.2 are known to cause spastic paraplegia 51 (SPG51). The exact phenotype of SPG51 remains poorly characterized, because only a few families have been reported as carriers of the mutation. In addition, a previous study identified an autosomal dominant mutation in the AP4E1 gene as being associated with persistent stuttering. The aim of the current study was to characterize the phenotype of a paediatric patient with an identified novel AP4E1 mutation presenting with significant psychomotor retardation, intellectual disability and paraplegia. Methods Magnetic resonance imaging was used to identify hypoplasia of the corpus callosum. The DNA sample was tested using multiplex ligation-dependent probe amplification (MLPA) and array comparative genomic hybridization (aCGH). In addition, next-generation sequencing (NGS) was performed using the patient’s DNA, and Sanger sequencing was performed using that of his family members. Results The phenotype was identified to be associated with a novel pathogenic variant c.942_943 + 3delinsCC in the AP4E1 gene. The patient manifested severely delayed psychomotor development, impaired global physical development and general illness. Movement disorders were evident during the neonatal period. Conclusions The present study identifies a previously unknown disease-inducing AP4E1 gene mutation.


Background
Spastic paraplegia-51 (SPG51; OMIM # 613744) is an autosomal recessive neurodevelopmental disorder that is characterized by the degeneration and dysfunction of the corticospinal and spinocerebellar tracts. Hypotonia in the neonatal period can progress to spasticity, hypertonia and severe intellectual disability, which is characterized by underdeveloped or non-existent speech. Moreover, cognitive and behavioural dysfunctions are notable [1,2]. Spastic paraplegia is often confused with cerebral palsy. However, spastic diplegia or quadriplegia are not associated with birth order or parental age, while the age of the parents is associated with congenital hemiplegia and dystonic/athetoid cerebral palsy [3].
AP-4 complex subunit ϵ − 1 (AP-4E1) is involved in recognizing and binding sorting signals that are tyrosinebased and located within cytoplasmic cargos. In addition, AP-4E1 is able to recognize various sorting signals. Previous studies suggested that AP-4E1 facilitates the sorting of proteins to the basolateral membrane in epithelial cells and is involved in the establishment of effective somatodendritic protein asymmetric localization in neurons [1][2][3][4].

Open Access
*Correspondence: ikochans@interia.pl 1 2nd Department of Gynaecology, St. Johns Centre Oncology, Lublin Oncology Centre, 7 Jaczewski Street, 20-090 Lublin, Poland Full list of author information is available at the end of the article AP-4-associated hereditary spastic paraplegia (HSP) is a group of neurodegenerative disorders that manifest as complex and progressive spastic paraplegia. Defects associated with HSP are typically identified during infancy or early childhood. Early-onset hypotonia becomes a progressive lower-extremity spasticity over time, and the patients affected by this disease are unable to walk or stand. Further progression of the spasticity affects the upper extremities, which leads to spastic tetraplegia. Additional complications include bladder and bowel dysfunction, dysphagia, foot deformities and contractures. In total, ~ 50% of patients experience seizures, and spastic paraplegia is associated with congenital microcephaly and global developmental delay. Furthermore, speech development is delayed, and speech is often absent [1,2,5].
The aim of this study was to characterize a novel mutation in the AP4E1 gene that is correlated with the phenotypic variability of affected patients.

Methods
The study was approved by local Ethics Committee. We obtained written informed consent for publication of the case file and clinical details from the patient's parents. The comprehensive evaluation in the study relied on a detailed clinical history and the review and analysis of past medical records. The paediatric patient was the fourth child of non-consanguineous parents of Polish nationality. The boy was born at term (gestational week 41) after an uneventful pregnancy. His weight at birth was 4,100 g (> 99.9 percentile), his length was 55 cm (99 percentile), and his head circumference was 36 cm (85-90 percentile). The proband was delivered by caesarean section due to incipient foetal distress. His brother showed a similar history and had spastic paraplegia, while the other two siblings were healthy. Serious psychomotor retardation and general illness were evident in the neonatal period. In addition, dysmorphic features were noted, including periodic bilateral ptosis, a wide nasal ridge and long nose, an inverted full upper vermillion and short philtrum, marked ear antihelix and hypomimia of the face. No internal organ abnormalities were found following physical examination and ultrasound assessment. Lack of head control, eye contact and social smiling, in addition to marked axial hypotonia with bouts of hypertonia in the extremities, were identified on neurological examinations. No additional abnormalities were identified in the first six months by the physicians or the parents. Hyperplastic corpus callosum was diagnosed by magnetic resonance imaging, but hyperammonaemias, mitochondrial fatty acid beta-oxidation disorders, aminoacidopathies, glycosylation congenital disorders, neurotransmitter disorders and organic acidurias were excluded. Occasional ptosis excluded mitochondrial disease. Spastic diplegia was identified on neurological assessment at 2 years and 6 months of age. Therefore, treatment with botulinum toxin was undertaken. The male karyotype, array comparative genomic hybridization (aCGH) and multiplex ligation-dependent probe amplification (MLPA) were normal. At the last examination, the paediatric patient (age, 12 years) was 128 cm tall (< 3rd percentile), weighed 37 kg (25th percentile) and had a head circumference of 51 cm (< 3rd percentile). He could not stabilize his neck or torso, nor could he vocalize or rotate. His arm and leg movements were uncoordinated and restless. The proband could not smile and showed no response to loud noise. The parents, however, did not report seizures. The proband could balance on his hands and knees, and movements were possible with the aid of a rear balustrade. Physiotherapy improved his lower limb muscle tone. Examination did not indicate ptosis, and Babinski's bilateral sign was not evident.
Blood was collected, and DNA was extracted for further examinations. MLPA was performed as the initial diagnostic step. To perform MLPA, a P106-B2 (MRC Holland) kit was used. Next, aCGH (CytoSure Constitutional v3, 8 × 60 k; Oxford Gene Technology; GRCh37/ hg19) was performed. The results of both test were normal. Further diagnostic procedures was performed using the NGS targeted SeqCap EZ (Nimle Gen) kit. For NGS analysis, the panel of 219 genes correlated with intellectual disability that was designed by the MedGen laboratory was used. The enriched DNA libraries were sequenced by the Illumina MiSeq instrument. The average depth of coverage for the AP4E1 gene was 100% per 30x.
Additionally, Sanger sequencing was performed for the patient and his family (parents and siblings).
We deposit the sequences in a publicly available data repository (ClinVar), the accession number is VCV001064645.1.

NGS
examination revealed the mutation c.942_943 + 3delinsCC in the AP4E1 gene (Fig. 1) located in the distal part of exon 8 and spanning two exonic and three intronic nucleotides, including a splicing donor site. Bioinformatic analysis using Alamut software predicted a new donor site, which resulted in a frameshift mutation introducing the premature termination of the codon after three nucleotides. It is also possible that the mutation may affect the splicing process (not examined in this study). The proband was homozygous for this mutation according to NGS. Sanger sequencing was used to confirm the presence of the variant in the paediatric patient and the following family members: his brother, who had spastic paraplegia; his other healthy siblings; and his parents (Fig. 2). The mutation c.942_943 + 3delinsCC in the AP4E1 gene identified in the present study was not reported in the ClinVar (ncbi.nlm.nih.gov), LOVD Year of birth is shown below square or circle (lovd.nl), ExAC (gnomad.broadinstitute.org) and dbSNP (ncbi.nlm.nih.gov/snp) databases. Therefore, this variant is considered a novel pathological variant that has not been previously reported. Moreover, the proband was heterozygous for the mutation p.Pro311Arg in the SMARCA4 gene. This mutation was registered in the dbSNP database (rs759754994) but was not reported in the ClinVar and LOVD databases. The SMARCA4 mutation was confirmed in the patient using Sanger sequencing, and his father was heterozygous. The presence of the SMARCA4 mutation in the unaffected father suggests a non-pathogenic nature of the mutation. In the other siblings, mutations in the SMARCA4 gene were not found; in particular, pathogenic variants in the SMARCA4 gene are correlated with Coffin-Siris syndrome (CSS4, OMIM#614609).

Discussion
The present study reported the case of a teenage boy with significant developmental delay, primary microcephaly and pyramidal-extrapyramidal tetraparesis. Cerebral palsy was initially diagnosed prior to genetic counselling. NGS was performed, and a disease-inducing mutation was found in the AP4E1 gene encoding the AP-4 adaptor protein complex subunit ϵ − 1. To the best of our knowledge, the current study is the first report confirming the pathogenicity of the c.942_943 + 3delinsCC mutation.
According to Abou Jamra et al. [1], AP4 complexmediated trafficking is crucial for brain development. In addition, this protein is involved in the formation of clathrin-and non-clathrin-coated vesicles and in integral membrane protein sorting. AP4 consists of 2 large chains, β-4 (AP4β1) and ϵ − 4 (AP4ϵ1); the medium chain, µ-4 (AP4µ1); and the small chain, σ-4 (AP4σ1) [5,6]. Knockout mice homozygous mutants exhibit abnormal white blood counts, enlarged lateral ventricles, a smaller corpus callosum and hypoferremia [6]. Additional mutations in the AP4E1 gene have been discovered. To date, ~ 80 individual mutations have been reported and included in the International Registry and Natural History Study of AP-4-Related Hereditary Spastic Paraplegia (updated 5-20-18). Considering the type of mutation (3delTG-GTAinsCC), which induces a frameshift mutation and occurs in the proximity of a splicing site, it can be predicted that the identified mutation may affect the splicing process. Bioinformatic analysis showed that the detected variant may cause a change in the acceptor site, which further indicates its pathogenic nature. The homozygous indel mutation was found in another member of the family, the affected brother of the proband.
The parents were heterozygous for this mutation, one unaffected sibling was wild type, and the other unaffected sibling was heterozygous. Numerous case reports have been published describing patients with SPG51, and the clinical phenotype observed in the present study is consistent with the symptoms observed in an individual reported in a case study by Moreno De Luca et al. [2]. In the present study, the investigated subject never developed speech or independent ambulation. A comprehensive mutational analysis (including resequencing), as well as an analysis of AP4E1 in other individuals with spastic paraplegia and in their families, should be undertaken to evaluate the frequency of this disorder.
Coffin-Siris syndrome, an autosomal condition, is caused by mutations in any of the following genes: ARID1A (AT Rich Interactive Domain 1A), ARID1B (AT Rich Interactive Domain 1B), SMARCA4 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4), SMARCB1 and SMARCE1 [7]. The clinical features of Coffin-Siris syndrome include thick, arched eyebrows; a low anterior hairline; a broad-tipped nose; a short philtrum; columella below the alae nasi; simple posteriorly rotated ears; and a thick drooping lower lip [8]. Moreover, hyperkeratotic plaques and rough skin are also common features of this disease. In addition, the fingertips and feet are frequently broader than normal (Table 1). Furthermore, Poyhonen et al. [8] showed a short, thick corpus callosum confirmed by brain MRI.
In the present case report, an autosomal dominant inheritance with variable expression and a possible paternal effect was identified. Family pedigree analysis indicated that the detected SMARCA4 mutation is most likely a benign variant. Over 94% of SMARCA4 gene missense changes are benign or are described as variants of uncertain significance (according to the TrapScore database).

Conclusions
The present study indicates that the c.942_943 + 3delin-sCC mutation in AP4E1 is a pathogenic variant. Thus, early molecular diagnosis may significantly enhance the diagnostic process, clinical management and genetic counselling of patients suffering from HSP and their families. However, further studies are needed to investigate the causal association between the clinical features and the mutation. Future studies may clarify the associations between the observed clinical features and genetic mutation. Following the identification of an AP-4-associated HSP-causing pathogenic variant in one member of the family, prenatal testing and pre-implantation genetic diagnosis should be considered.