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October 2020; 6 (5) ArticleOpen Access

Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy

William W. Motley, Stephan Züchner, Steven S. Scherer
First published July 31, 2020, DOI: https://doi.org/10.1212/NXG.0000000000000496
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Abstract

Objective To determine the genetic cause of axonal Charcot-Marie-Tooth disease in a small family with 2 affected siblings, one of whom had cerebellar features on examination.

Methods Whole-exome sequencing of genomic DNA and analysis for recessively inherited mutations; PCR-based messenger RNA/complementary DNA analysis of transcripts to characterize the effects of variants identified by exome sequencing.

Results We identified compound heterozygous mutations in dystonin (DST), which is alternatively spliced to create many plakin family linker proteins (named the bullous pemphigoid antigen 1 [BPAG1] proteins) that function to bridge cytoskeletal filament networks. One mutation (c.250C>T) is predicted to cause a nonsense mutation (p.R84X) that only affects isoform 2 variants, which have an N-terminal transmembrane domain; the other (c.8283+1G>A) mutates a consensus splice donor site and results in a 22 amino acid in-frame deletion in the spectrin repeat domain of all BPAG1a and BPAG1b isoforms.

Conclusions These findings introduce a novel human phenotype, axonal Charcot-Marie-Tooth, of recessive DST mutations, and provide further evidence that BPAG1 plays an essential role in axonal health.

Glossary

cDNA=
complementary DNA;
CMT=
Charcot-Marie-Tooth;
MRC=
Medical Research Council;
SR=
spectrin repeat;
WES=
whole-exome sequencing

Embedded Image

Charcot-Marie-Tooth (CMT) disease, also called hereditary motor and sensory neuropathy, is among the most common neurogenetic diseases and is characterized by progressive length-dependent weakness and sensory loss. CMT is divided into demyelinating (type 1) and axonal (type 2) forms of the disease based on clinical, electrophysiologic, histologic, and genetic features.1 Recessively inherited demyelinating neuropathies are called CMT4, whereas recessively inherited axonal neuropathies are called autosomal recessive (AR)-CMT (ncbi.nlm.nih.gov/omim/). Over 80 genes have been linked to CMT and related disorders; 13 of which have been associated with AR-CMT2.

Next-generation DNA sequencing has facilitated the identification of disease-causing mutations in small families with CMT.2 To determine the cause of AR-CMT in a small family with 2 affected individuals, we performed whole-exome sequencing (WES) and identified 2 rare compound heterozygous variants in the dystonin gene (DST; MIM: 113810). The protein product of the DST gene is an alternatively spliced cytoskeletal linker protein named the bullous pemphigoid antigen 1 (BPAG1), so named because one of its isoforms (BPAG1-e) is the autoimmune target in the blistering skin disease.3 Two human genetic diseases have been linked to mutations in DST: recessively inherited mutations in DST that only affect the BPAG1-e isoforms cause epidermolysis bullosa simplex (EBSB2),4,5 and recessively inherited mutations cause hereditary sensory and autonomic neuropathy (all referred to as HSAN-VI), the severity of which depends on the isoforms that are affected.6,–,10 Here, we characterize the mutations identified in 2 patients with an axonal neuropathy caused by mutations in DST and show that together they selectively affect BPAG1-a2 and BPAG1-b2 isoforms. This work identifies a novel cause of AR-CMT, introduces a novel phenotype for DST-linked axonopathies, and supports an essential role of BPAG1 in axonal health.

Methods

Protocol approvals and patient consents

Institutional Review Board approval was obtained from the University of Pennsylvania for these studies. Written informed consent was obtained from each patient who participated.

Clinical data and sample collection

Each living family member was seen by S.S.S. in an outpatient clinic, where an examination using the Medical Research Council (MRC) scale for strength was used, and clinical neurophysiology was also performed with standard methods.

WES and analysis

Genomic DNA was isolated from peripheral blood from all participants. Exome DNA was captured using the SureSelect, Human All Exon5 50 Mb kit (Agilent, Santa Clara, CA) and sequenced on a HiSeq 2000 (Illumina, San Diego, CA). Paired-end reads of 100 bp length were generated, and alignment and variant calls were made using BWA11 and genome analysis toolkit software packages.12 Using Genesis,13 variants were filtered for missense, nonsense, frameshift, stop gained or lost, splice site variants, deletions, and insertions that met the following criteria: high evolutionary conservation scores (if a missense mutation: PhastCons > 0.5, phyloP > 1.5), low allele frequencies in large data sets (<0.01 in ExAC and gnomAD, <0.002 in Genesis), and good sequence quality (read depth > 12, genome quality filter GQ > 75, and quality filter QUAL > 50), which segregated with disease in a recessive inheritance pattern. Two missense changes (p.Pro2950Ser and p.Ile559Val) in the REV3L gene, which encodes a DNA polymerase zeta subunit protein, cosegregated but were present in gnomAD in 3 and 125 individuals, respectively. The DST variants were confirmed by bidirectional Sanger sequencing.

Transcript analysis

RNA was isolated from skin using the ZR-Duet DNA/RNA MiniPrep Plus kit (Zymo, Irvine, CA). Complementary DNA (cDNA) was reverse transcribed using SuperScript III First-Strand Synthesis System (Invitrogen, Waltham, MA). cDNA was PCR amplified using Platinum Taq (Invitrogen) using forward (5′-GTTCCAGACTGTAGAGGCCCAATTG-3′) and reverse (5′-GCTGAAATTGATGAGAGCTTGCACA-3′) primers. The BPAG1-e isoform was amplified using forward (5′-TGCAGCAAGGGCAGCACATGGAAGCA-3′) and reverse (5′-GCCTGGCAGTCACAGTGTGCCTAAGCC-3′) primers. β-tubulin (TUBB) was amplified using forward (5′-CTGTTCGCTCAGGTCCTTTTGG-3′) and reverse (5′-GGTGTGGTCAGCTTCAGAGTGC-3′) primers. Mutant transcript sequence was isolated after PCR products were cloned using TOPO TA Cloning Kit for Sequencing and Sanger sequenced using traditional methods.

Mutation mapping

Our description of the 2 mutations observed in our patients follows Human Genome Variation Society nomenclature guidelines (hgvs.org/mutnomen) and is based on sequence from the following transcripts: our mutations are annotated based on BPAG1-a2, RefSeq transcript NM_001144769; the HSAN-VI mutations are also annotated based on BPAG1-a2, RefSeq transcript NM_001144769; and the EBSB2 mutations are annotated based on BPAG1-e, RefSeq transcript NM_001723. The location and number of predicted spectrin-repeat (SR) domains were determined based on previous publications14,15 and personal communications with the authors. The SR domain structure from the plakin domain was downloaded from the Protein Data Bank (accession number 2IAK16) and viewed and annotated using PyMol software (pymol.org).

Results

Clinical data

Our proband (II.3) first noted difficulty walking at age 13 years, difficulty with balance at age 15 years, and required foot orthotics at age 20 years. She was first seen in our clinic at age 29 years, when she was diagnosed with axonal CMT. At that time, she was unable to plantar flex, dorsiflex, or evert the foot at the ankles (MRC, 0/5), and the posterior and anterior compartment muscles of the calves had marked atrophy. Proximal leg muscles were strong. In the upper extremities, there was moderate weakness (4/5) and mild atrophy of the interosseous and thenar muscles and slight weakness of finger extension. There was decreased appreciation to pin prick and light touch until above the ankles and a mild proprioceptive deficit. Deep tendon reflexes were absent at the ankles, 1+ at the knees, and 2+ at the triceps and biceps. Plantar responses were muted. She had a positive Romberg sign and had significant difficulty with tandem walking and had been wearing leg braces for several years—without these braces, she walked with a steppage gait. Weakness of intrinsic hand muscles had progressed to 4−/5 by 1999, and mild weakness of the quadriceps and hamstrings was noted. Falling became an issue at age 51 years; at age 53 years, she started using a cane and progressed to using a walker by age 55 years. From 2010 to 2019, her CMT neuropathy score increased from 23 to 29.17 EMGs were performed at age 29, 35, 45, and 64 years (table 1), showing progressively smaller amplitudes of the sensory and motor compound action potentials. Thus, she has a length-dependent, sensory and motor axonal neuropathy that worsened over time.

View this table:
Table 1

Nerve conduction studies of affected patients

She also developed some additional findings. She had an abnormal electronystagmogram at age 30 years, with saccadic pursuit movements, but these were not evident on clinical examination at that time, and brainstem auditory evoked potentials were normal. At age 49 years, she had scanning speech, eye movements with broken smooth pursuits, and abnormal finger-to-nose and rapid alternating movements in the hands, all indicative of a cerebellar disorder. Nystagmus in primary gaze and scanning speech were noted at age 56 years. Brain MRI at age 60 years was normal; it did not show cerebellar atrophy (not shown).

Her younger brother (II.4) has been followed in our clinic since 2003, when he was aged 46 years. He had been diagnosed with CMT around age 18 years with a similar clinical course. At age 47 years, he was noted to have difficulty executing rapid alternating movements with his hands and trouble performing heel-to-shin movements. He has not developed abnormal eye movements or scanning speech. From 2010 to 2019, his CMT neuropathy score increased from 21 to 26. EMGs were performed at age 46, 53, and 59 years (table 1) and show a severe, progressive, sensory, and motor axonal neuropathy. Their eldest sibling (II.1) and their father (I.1) were examined at separate times and did not have neuropathy.

DST mutations

We performed WES on all 3 living siblings. After sorting for variants based on stringency criteria, DST was the only gene with variants not present in gnomAD that cosegregated in a recessive inheritance pattern. One mutation (c.250C>T; GRCh38 Chr6:56,900,588G>A) is a nonsense mutation that is predicted to cause a premature termination of the protein (p.R84X); the other mutation (c.8283+1G>A; GRCh38: 56,557,318C>T) alters a consensus splice donor site. Both mutations are present in the 2 affected individuals (II.3 and II.4), whereas only 1 (c.250C>T) is present in the unaffected sibling (II.1), showing that the mutations are in trans (figure 1, A and B). Neither variant is present in gnomAD, in the NHLBI exome variant server, or in the ∼13,000 exomes in Genesis.

Figure 1
Figure 1 Compound heterozygous DST variants segregate with neuropathy, and mapping the mutations in the DST gene structure predicts isoform-specific loss of function

(A) The pedigree of the family. The proband (arrow) and her affected brother (II.3 and II.4, respectively) as well as their 2 unaffected older siblings (II.1 and II.2) and unaffected parents (I.1, I.2) are shown, along with the genotypes of all living members (II.1, II.3, and II.4). One mutation (c.250C>T) is present in all 3 siblings; the second mutation (c.8283+1G>A) is only present in the 2 affected individuals (II.3 and II.4). The segregation of these DST variants is consistent with recessive inheritance from their unaffected parents. (B) Sanger sequencing was used to confirm the genotypes gathered by whole-exome sequencing. The chromatograph traces of the 2 variants are shown for all 3 members of the family. (C) The exon structure of DST. Exons are numbered for the entire gene, not for specific transcripts; the width of the exons is proportional to their length. There are 107 exons and 4 transcription initiation sites, each of which gives rise to the named transcripts—1: a2, b2; 2: a1, b1, n; 3: a3, b3; 4: e. The 4 alternative promoters and the 3 alternative splicing events (dotted lines) produce the 8 isoforms of BPAG1 shown in figure 2. The protein domains encoded by the exons are indicated with brackets below the exons (abbreviations are explained in figure 2). The genomic locations of the mutations identified in our patients are shown in red, the homozygous and compound heterozygous mutations associated with HSAN-VI are shown in magenta and green, respectively, and the mutations associated with EBSB2 are shown in purple. (D) PCR amplification of skin complementary DNA from a control and the 2 affected patients shows that the c.8283+1G>A mutation (part of the dinucleotide-gt-splice donor site at the 3′ end of exon 63) results in incorrect splicing and deletion in the transcript. BPAG1-e and β-tubulin expression is similar between the control and patient samples. (E) Cloning and sequencing of that aberrant transcript reveals an in-frame 66 bp deletion, which results from the use of a cryptic GT splice donor site within exon 63.

DST has a large (107 exons), highly complex gene structure that is similar in humans and mice. Four transcription initiation sites and alternative splicing produce 8 isoforms of BPAG1 (figures 1C and 2A). The most 5′ transcription initiation sites encode the N-terminus of isoform variants BPAG1-a2 and BPAG1-b2, the only isoforms with a transmembrane domain. Because the p.R84X mutation is in 1 of the 4 exons that are related only to the BPAG1-a2 and BPAG1-b2 isoforms (figure 1C), it is predicted to cause the loss of the BPAG1-a2 and BPAG1-b2 isoforms and to not affect the other 6 isoforms (BPAG1-e, BPAG1-n, BPAG1-a1, BPAG1-a3, BPAG1-b1, and BPAG1-b3). The c.8283+1G>A variant lies in the GT dinucleotide splice donor site, 1 base pair downstream of exon 63 (numbered based on the entire genomic locus; this corresponds to exon 53 in the a2 isoform), which encodes part of the SR domains that are present in all BPAG1-a and BPAG1-b transcripts (figure 2A).

Figure 2
Figure 2 Protein isoforms of BPAG1 and disease-associated mutations

(A) The 8 isoforms of BPAG1 and their functional domains are illustrated—transmembrane domain (TM); actin binding domain (ABD), composed of 2 calponin homology domains (CH1 and CH2); plakin domain (including 8 spectrin repeats [SRs] and an SH3 domain), coiled-coil domain (CC), plakin repeat domains 1 and 2 (PRD1 and PRD2), spectrin repeat domain, EF-hand calcium-binding domain (EF), and a microtubule-binding domain (MTBD). Two recessively inherited nonsense mutations that cause EBSB2 result in truncation (p.Q1124X and p.R1249X; purple dotted line) affect BPAG1-e and BPAG1-n isoforms. The recessively inherited mutation associated with congenital-onset HSAN-VI results in truncation (p.E5133fsX28; magenta dotted line) of all BPAG1-a and BPAG1-b isoforms. The compound heterozygous mutations associated with HSAN-VI (p.A203E, p.R206W, p.H269R, p.R1296X, and p.K4330X; green) are in multiple parts of the protein and have different impacts on BPAG1-a and BPAG1-b subisoforms. The p.R84X mutation that we report here (red dotted line) is predicted to result in premature truncation of only the BPAG1-a2 and BPAG1-b2 isoforms. The p.2740_2761del that we report here (red dotted line) falls in one of the SRs, within the range of a putative ezrin-radixin-moesin domain that is thought to associate with p150Glued.19 (B) Clustal Omega alignment of the SR12 (based on numbering from Jefferson et al.16), which is affected by the p.2740_2761del deletion, shows a high level of conservation across species. The amino acid sequences of the 3 helices that make up this trihelical SR domain are illustrated. The red dashed lines show the deleted amino acids. Highlighted in magenta are fully conserved amino acids; highlighted in blue are positions with conservation between amino acid groups with similar properties, and highlighted in green are positions with conservation between amino acid groups of weakly similar properties. (C) The Clustal Omega alignment of SR12 is compared with 2 SR domains in the plakin domain of human BPAG1 equivalent to the mouse SR domains that have been crystalized. The regions of the triple helical domains that are homologous to SR12 deletion are also boxed in a red dashed line. (D) The crystal structure of 1 SR domain from the plakin domain, embedded within a drawing of 4 surrounding triple helical structures, shows how the SRs fit together to create an elongated structural protein. Helix C is often contiguous with helix A from the subsequent SR domain. The regions of helices A and B that are deleted in our patients are shown in red in the crystal structure.

To characterize further the c.8283+1G>A variant, we took advantage of the fact that some BPAG1 isoforms containing the affected SR domain are also expressed in skin. PCR amplification of cDNA from punch biopsies from patient skin and a control using primers flanking the splice site in the SR domain revealed a shorter transcript in both patients (figure 1D). Sequencing clones of this shorter transcript revealed a 66 bp deletion (c.8218_8283del, annotated based on transcript a2), showing that a cryptic dinucleotide splice site within the coding exon is used instead of the mutant splice site (figure 1E); this is predicted to cause an in-frame deletion of 22 amino acids (p.2740_2761del; figure 2A). Alignment of the SR domain affected by the deletion shows that it is highly conserved (figure 2B). SR domains are triple helical protein structures, often organized in tandem repeats to form long elongated cytoskeletal proteins; helix C from the previous SR is often contiguous with helix A. The region that is deleted in our patients contains the last 4 residues in helix A, the linker between helices A and B, and the first 10 residues of helix B. Although the SR domain mutated in our patients (SR12 based on sequences from an annotation with a total of 32 SR domains16) has not been crystalized, the SR domains in the plakin domain of mouse BPAG1 have been crystalized16 (residues 580–802, annotated based on protein NP_604443.2). Figure 2C shows an alignment of human SR12 and the human SR1 and SR2 (orthologous to the SR domains from mouse protein that have been crystalized), and figure 2D shows the position of the p.2740_2761del on this crystal structure.

Discussion

DST encodes BPAG1, which has multiple isoforms (even more than are shown in figure 2A) that are expressed in a cell type–specific manner.18 BPAG1-a, -b, -e, and -n were the first to be described; when 3 more N-terminal variants were discovered (the result of alternative promoters), the terms 1, 2, and 3 were introduced for BPAG1-a and BPAG1-b isoforms (BPAG1-a1, -a2, and -a3; BPAG1-b1, -b2, and -b3; figure 2A). BPAG1 isoforms have varied functions, including cytoskeletal linker proteins with key functional domains connecting actin filaments, intermediate filaments, and microtubules,18 so that the loss of BPAG1 is thought to disrupt axonal transport through direct interactions with dynactin p150Glued,19 retrolinkin,20 and microtubule-associated protein 1B.21

The p.R84X mutation is predicted to abolish the expression of BPAG1-a2 and BPAG1-b2, but not the other BPAG1 isoforms, which are initiated by downstream alternative promoters (figures 1 and 2). The messenger RNA containing this mutation would be predicted to be degraded by nonsense mediated decay.22 The c.8283+1G>A variant changes a consensus residue in a splice donor site, resulting in a 66 base pair/22 amino acid deletion in the SR domain that is predicted to affect all BPAG1-a and -b isoforms (-a1, -a2, -a3, -b1, -b2, and -b3), but not BPAG1-e and -n (figure 2A). If this mutation produces an in-frame mutation, it may lead to hypofunction of BPAG1-a and BPAG1-b isoforms that play an essential role in primary sensory and motor neurons. With this in mind, it is particularly interesting that the mutation is adjacent to a putative ezrin-radixin-moesin domain18,19 that has been implicated as essential for axonal transport.19,20 In-frame deletion in SR domains can result in partial loss-of-function phenotypes: short deletions in the SR domain of dystrophin cause Becker muscular dystrophy, where truncating mutations cause the more severe Duchenne muscular dystrophy.23

We described 2 siblings with a progressive, sensory and motor axonal neuropathy over 4 decades. Cerebellar clinical findings emerged later, and autonomic symptoms/signs were not apparent even after age 60 years. In keeping with the absence of blistering skin, seen in patients with recessive mutations in the coiled-coil domain of BPAG1-e and BPAG1-n isoforms, the mutations in our patients did not affect these isoforms (figure 2A). Conversely, patients with EBSB2 do not have neuropathy.4,5,24

Our siblings also differ from the 4 reports of HSAN-IV caused by DST mutations (table 2). A homozygous frameshift mutation near the end of an SR domain (p.E4995fsX28 when annotated in isoform a1 or p.E5133fsX28 annotated in isoform a2) likely affects all BPAG1a and BPAG1b isoforms (figure 2A) in a single, consanguineous family. Affected infants have a severe and lethal phenotype—dysautonomia, feeding difficulties, respiratory insufficiency, distal contractures, hypotonia, absent deep tendon reflexes, and severe psychomotor retardation and facial paralysis. Subsequently, compound heterozygous DST mutations with milder, more discrete phenotypes have been reported in 3 families6,7,10; all had normal growth without cognitive deficits or developmental delay, as well as a severe sensory neuropathy affecting small and large fibers and complicated by painful ulcerations and amputations of the distal extremities. They also have had prominent autonomic symptoms, including hyperhidrosis, hypohidrosis, heat intolerance, chronic diarrhea, sexual dysfunction, and absent pupillary light reflexes. In 1 of these 3 families, 1 mutation (p.H269R) affects a1, b1, a2, b2, and n isoforms, whereas the second mutation (p.R1269X) affects the plakin domain, which is present in all isoforms; this patient had complex phenotype with blistering skin and some unique phenotypic features—including congenital cataracts, syringomyelia, and reduced growth hormone secretion. In the other 2 HSAN-IV families, one of the mutations (p.A203E and p.R206W) is predicted to selectively affect the a2 and b2 isoform, and the other mutation is predicted to have additional effects: the p.K4330X mutation (paired with the p.A203E mutation) should affect all BPAG1a and BPAG1b isoforms, and the c.687+1G>A mutation (paired with the p.R206W mutation) has an unknown effect (figure e-1, links.lww.com/NXG/A304, but should be restricted to the a1, a2, b1, b2, and n isoforms). Like these 2 HSAN-IV families, our family has 1 mutation (p.R84X) that selectively affects the a2 and b2 isoforms; the second mutation (p.2740-2761del) in our family should affect all BPAG1a and BPAG1b isoforms.

View this table:
Table 2

Genetic comparison of patients with DST-related neurologic disorders

Thus, the loss of a2 and b2 isoforms is correlated with axonal neuropathy (table 2; see also reference 25), and we infer that the additional phenotypes seen in the 2 families with additional features beyond HSAN1-IV likely owe to the additional loss of a1/b1, a3/b3, and/or n isoforms. This conclusion is in line with studies of recessive Dst mutations that produce the dystonia musculorum (dt/dt) phenotype in mice—an early-onset, progressive sensory neuropathy and ataxia notable for bizarre movements and abnormal postures. Pathologic analysis reveals that sensory neurons and their axons are the most affected,26 but spinocerebellar degeneration27 and motor axon involvement have been noted.28 Several Dst alleles have been identified, and the ones have been characterized share functional deletion of all a1 and b1 isoforms,18 including dttg4/tg4, which eliminates the expression of a1, a2, b1, and b2 (but not a3 and b3).29,30 Furthermore, expressing the a2 isoform as a transgene in neurons reduced the severity of dttg4/tg4 phenotype.31 Thus, the loss of BPAG1-a2 specifically could be the cause of the neuropathy seen in dt/dt mice and our patients; whether the loss of b2 contributes to the phenotype remains to be determined. Haploinsufficiency in several Dst alleles in mice has not been shown to cause any overt behavioral phenotypes, but dttg4/+ mice do have subtle ultrastructural defects in myelination of ventral roots and reduced axon caliber.32

Why somatic (motor and sensory) axons are more affected (and cerebellar axons are affected in one of our patients), whereas autonomic axons are not affected in our siblings, however, remains unexplained. The similarity between the mutations in the BPAG1-a2 and -b2 specific exons allows us to favor a hypothesis that the SR domain deletion (p.2740_2761del) confers this difference. The in-frame deletion in the SR domain produced by this mutation may result in a partial and selective loss of function, but how this mutation spares autonomic axons remains to be determined.

Study funding

This work was supported by the Judy Seltzer Levenson Memorial Fund for CMT Research, the INC (U54NS065712), which is a part of the NCATS Rare Diseases Clinical Research Network (RDCRN), an initiative of the Office of Rare Diseases Research (ORDR), NCATS, funded through a collaboration between NCATS and the NINDS, and WWM was supported in part by NIH (NINDS) R25NS065729.

Disclosure

W.W. Motley is a full-time employee of Third Rock Ventures. S. Züchner and S.S. Scherer report no relevant disclosures. Go to Neurology.org/NG for full disclosure.

Acknowledgment

The authors thank their patients and their sibling for their participation in this study, as well as Drs. Arthur Asbury, Mark Brown, and Kenneth Fischbeck for performing the initial evaluations. They thank Drs. Ronald Liem and Rashmi Kothary for their help with the structure of the dystonin gene and protein. They also thank Matt C. Danzi for help analyzing the primary sequencing data.

Appendix Authors

Table

Footnotes

  • Go to Neurology.org/NG for full disclosures. Funding information is provided at the end of the article.

  • The Article Processing Charge was funded by the authors.

  • Received March 8, 2020.
  • Accepted in final form May 28, 2020.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND), which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

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