A novel nonsense mutation in WNK1/HSN2 associated with sensory neuropathy and limb destruction in four siblings of a large Iranian pedigree

Hereditary sensory and autonomic neuropathies (HSANs) are inherited group of neurodegenerative disorders of the peripheral nervous system associated with sensory dysfunction [1]. HSAN is characterized by the multimodal loss of sensation with or without presentation of autonomic disturbances [2]. In this group of neuropathies, motor neurons are relatively or entirely spared [3]. Based on clinical features and pattern of inheritance, HSAN has been categorized into seven types with additional entities related to mutations in different genes [4].

HSAN type 2 (HSAN2) was first described in 1973 by Ohta M. et al. [5], but its genetic etiology was initially demonstrated from Canadian patients in 2004, and causative mutation was reported in an intron within the WNK1 gene, referred to as HSN2 [6]. HSAN2 occurs sporadically or with autosomal recessive inheritance pattern, which is usually diagnosed during the first two decades of life [7]. Predominantly, HSAN2 patients present sensory deficit in distal lower limbs more severely than the upper ones with possible motor involvement and variable autonomic disturbances. With the passing of time, ulcero-mutilating complications will be revealed and, the disease can become more complicated by osteomyelitis and painless fractures [2, 8]. This disorder doesn’t have a sex preference or particular ethnic distribution [9].

The recommended approach taken to the diagnosis of HSAN2 is based on detailed family history, clinical and paraclinical findings comprising neurological examinations in order to determine the extent of sensory loss and involvement of autonomic and motor nervous system, electrophysiology, histopathological evaluation of sural nerve and molecular genetic testing of candidate genes [8]. Nowadays, the genetic methods such as next-generation sequencing (NGS) based methods, are good opportunities to reduce the requirement of invasive diagnostic tests such as histological evaluation [10].

HSAN type 2 is classified into four subtypes including HSAN2A, HSAN2B, HSAN2C and HSAN2D that respectively are ascribed to genes HSN2, FAM134B, KIF1A and SCN9A in which several mutations are known to develop the diseases [11‐13].

HSN2 (NM_213655) is a single-exon gene located within intron 8 of WNK1 (WNK lysine deficient protein kinase 1). WNK1/HSN2 appears to be expressed in satellite and Schwann cells, and sensory neurons [14]. Various HSN2 mutations have been reported from patients with different ethnicity causing HSAN2 [1, 6, 14, 15]. Herein, we report a novel nonsense mutation in WNK1/HSN2 associated with the clinical presentations of HSAN2 in four siblings of an Iranian family.

An HSAN2 pedigree with four affected and one unaffected sibling was recruited (Fig. 1a). The HSAN2 diagnosis was made based on clinical criteria, the results of electrophysiological evaluations, audiometry and tympanometry tests and laboratory assessments. The clinical features of the patients were recorded and summarized in Table 1.

With-no-lysine (K) kinase 1 (WNK1), lysine deficient protein kinase 1, a gene located on 12p13.33, consists of 28 coding exons and encodes multiple isoforms of serine/threonine-protein kinase WNK1. WNK1 proteins regulate the activity of other proteins by attaching the phosphate group to specific positions. Due to the protein kinase properties, WNK1 isoforms can control the fluxes of sodium and chloride ions and have been considered as one of the primary regulators of blood pressure. Accordingly, several mutations resulted in WNK1 over-expression have been reported as the causative mutations of an autosomal dominant disorder, pseudohypoaldosteronism type II, which is characterized by hypertension, hyperkalemia, and renal tubular acidosis [8, 16]. In summary, it has been suggested that WNK1 proteins in cooperation with the other WNK kinases and with mediation of kinases SPAK and OSR1 have role in renal epithelial transport, maintaining cell volume homeostasis, GABA signaling, immune function and cell migration through the effect on cation-Cl⁻ co-transporters [17].

HSN2 is an alternatively spliced exon in WNK1 providing the nervous system specific isoform of WNK1 transcript, namely WNK1/HSN2 [14]. It has been hypothesized that WNK1/HSN2 product involves the control of neuronal ion transportation and affect membrane excitability. Furthermore, several lines of studies have been shown this protein regulates neurite extension via its effect on Nogo signaling during neuronal differentiation [18, 19]. To date, 20 homozygous mutations in WNK1/HSN2 have been reported and almost all are in the HSN2 exon leading to truncating and loss-of-function [15] and WNK1/HSN2 protein leads to HSAN2A disease [6, 20‐23]. Analyzing the results of genetics evaluations including Sanger sequencing of previously reported mutations as well as exome sequencing showed that none of the previously reported variations for HSAN2 were present in this family, but a novel nonsense mutation c.3718C > A in HSN2 exon of WNK1 transcript was found that resulted in alteration of the tyrosine codon TAC to the stop codon TAA and a truncated protein with 1025 amino acids. This result has been confirmed by subsequent segregation analysis and introduced c.3718C > A as a novel mutation for HSAN2A.

Clinical symptoms of the prior reported HSAN2A patients characterized within first two decades of life with predominant sensory polyneuropathy manifested most profound distally in a glove-stocking distribution. Sensory neuropathy was reported in lower limbs more severely than the upper limbs, although the trunk was involving in some patients. In addition, the previously reported patients presented with decreased or absent of DTRs, limb ulceration and mutilation with or without muscle weakness and variable autonomic disturbances [6, 15, 21, 23]. Our studied patients’ clinical characteristics include reduced perception to pain, touch, sense of temperature, and vibration and position sensation in distal areas of upper and lower extremities with more severity in the lower limbs. They express reduced DTRs, limb mutilation and amputation, with unremarkable autonomic clinical examination without motor dysfunction (Table 1) which are consistent to the clinical presentations of previously reported data in patients with HSAN2A [8].

Clinical presentations, inheritance pattern, and genetic analyses in our reported patients confirmed the HSAN2A diagnosis by identification of a novel mutation. It is worth mentioning there are several reports of HSAN2 patients from Iran but none of them conducted genetic investigations [24‐27]; thus the current study is the first report of HSAN2A in Iranian patients with complementary genetic analyses. Detection of this new mutation in HSN2 presents allelic heterogeneity of this gene in different populations.

Consistent with previously reported mutations in HSN2 exon, the novel mutation identified in the current Iranian HSAN2 pedigree also leads to a truncating loss-of-function mutation. Therefore, the result of present study expands the spectrum of mutations of the HSN2 gene as the genetic background of HSAN2A as well as further support the hypothesis that HSN2 is a causative gene for HSAN2A. However, more research is required to determine the exact effects of this mutation in the nervous system. Moreover, the relevance of WNK1/HSN2 transcript and its pathogenic mutations to HSAN needs more deciphering.