Autosomal dominant myopathy caused by a novel ISCU variant

Hereditary myopathy with lactic acidosis due to Iron-Sulfur Cluster Assembly Enzyme (ISCU) deficiency is a rare disorder of energy metabolism characterized clinically by myopathy with exercise intolerance, and biochemically by deficiencies of skeletal muscle mitochondrial respiratory chain enzymes. ISCU protein plays an important role in iron-sulphur clusters (Fe-S) assembly and is therefore essential for the activity of mitochondrial Fe-S proteins such as succinate dehydrogenase and aconitase. Recessive hypomorphic ISCU alleles have been associated with hereditary myopathy with lactic acidosis, also known as Swedish-type myopathy. To date, only one heterozygous dominant variant (c.287G>T, p.Gly96Val) in the ISCU gene has been reported as pathogenic. Functional studies have shown that this variant has a detrimental, dominant effect on activity of Fe-S-dependent enzymes. Whole exome sequencing performed in an adult female patient with progressive muscle weakness led to the identification of a novel heterozygous variant c.399del (p.Val134Ter) in the ISCU gene. This variant is localized in the functional IscU_like domain of the ISCU protein, with bioinformatics prediction of damaging effects on protein function. Moreover, the same variant was also found in a few family members, who present signs of myopathy. This novel variant segregates with the disease and results in a phenotype reminiscent of the recessive disease previously reported. Yeast Saccharomyces cerevisiae is a widely used tool able to assess the impact of the VUS in a quick and efficient way, therefore functional studies were performed on this model system. The results obtained not only confirm the pathogenetic effect of the variant, but also support its dominant inheritance.

Introduction

The ISCU gene (12q23.3; HGNC ID: 29882) is composed of 5 exons (983 nucleotides; NM_213595.4) and encodes a 15 kDa protein of 167 amino acid residues (NP_998760.1) performing a scaffolding function during iron-sulfur clusters assembly. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol (isoform 1 NM_014301.4) or to the mitochondrion (isoform 2 NM_213595.4) (Tong and Rouault, 2000). Isoform 1 contains an alternate exon in the 5′region and initiates translation at an alternative start codon compared to variant 2. Therefore, the cytosolic isoform has a distinct, shorter N-terminus. Mitochondrial isoform 2 encodes the longest transcript.

The ISCU structure consists of four α-helices which arc around the three antiparallel β-strands to form a planar platform for the molecule (Campbell et al., 2021). The active site, containing three conserved cysteine residues (Cys69, Cys95 and Cys138) and an aspartic acid residue (Asp71) (Fox et al., 2019), provides the setting where sulfur is delivered as a persulfide by cysteine desulfurase (NFS1) with the assistance of frataxin (FXN). Once iron is delivered, both substrates are used for Fe–S cluster assembly (Fox et al., 2019). Fe-S clusters are fundamental to numerous biological processes. They play a role in the functioning of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, DNA synthesis and repair, ribosome biogenesis, and oxidative stress response (Kollberg et al., 2009; Legati et al., 2017). Inability to express a full-length functional ISCU in humans results in Fe–S cluster deficiency, emphasizing the scaffold’s importance in relation to the cluster assembly pathway (Campbell et al., 2021).

Pathogenic/likely pathogenic variants in the ISCU have been linked to mitochondrial and neuromuscular disorders, manifesting in a variety of phenotypes. Hereditary myopathy with lactic acidosis due to ISCU deficiency is a rare disorder (MIM #255125) of energy metabolism characterized clinically by myopathy with severe exercise intolerance and biochemically by deficiencies of skeletal muscle mitochondrial respiratory chain enzymes, succinate dehydrogenase and aconitase. This mitochondrial myopathy is classically characterized by lifelong exercise intolerance in which minor exertion causes tachycardia, shortness of breath, fatigue and pain in active muscles. Episodes of more profound exercise intolerance are associated with rhabdomyolysis, myoglobinuria, and weakness. Affected individuals can have calves hypertrophy (Larsson et al., 1964; Haller et al., 1991; Kollberg et al., 2009; Kollberg et al., 2011).

So far, this disease has been molecularly identified in few patients: Swedish patients, homozygous for a deep intronic splicing affecting mutation in the ISCU (c.418 + 382G>C, also known as IVS5+382G>C, reported in ClinVar - a public archive of reports of human variations classified for diseases with supporting evidence - as a pathogenic variant) (Mochel et al., 2008; Olsson et al., 2008); a single Scandinavian family with a missense change in compound heterozygosity with the common intronic variant (c.418 + 382G>C and c.149G>A, p.Gly50Glu (reported in ClinVar as a likely pathogenic variant) (Kollberg et al., 2009) and an Italian patient heterozygous for the de novo dominant ISCU variant (c.287G>T, p.Gly96Val, not reported in ClinVar) (Legati et al., 2017). A disease-associated mutation in an intron (c.418 + 382G>C) activates a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein (Nordin et al., 2011). Homozygosity for the common pathogenic splice site variant results in a mitochondrial disorder restricted to skeletal muscle with characteristic features of severe exercise intolerance. In Sweden, the carrier rate has been estimated at 1:188 (Mochel et al., 2008). Although data is limited, reported individuals, who are compound heterozygotes for the common pathogenic splice site variant and a missense variant, have had a more severe muscle phenotype with weakness and cardiomyopathy (Kollberg et al., 2009).

More recently, a heterozygous, de novo dominant ISCU variant (c.287G>T, p.Gly96Val) was reported in a patient with isolated myopathy and moderately high creatinine kinase (CK) and no involvement of other organs (Legati et al., 2017). Clinical, histological, histochemical and biochemical abnormalities affecting skeletal muscle were similar to those reported for ISCU recessive pathogenic/likely pathogenic variants, including a partial depletion of SDH and COX histochemical reactions, a generalised reduction of the mitochondrial respiratory chain complex activities, and the accumulation of iron deposits. Moreover, analysis of the corresponding genetic defect in yeast suggested a Fe-S protein biogenesis defect, including defects in OXPHOS and in cellular iron regulation. The effects were dominant, since both the monoallelic and the heteroallelic genotypes were associated with the phenotype (Legati et al., 2017).

In this paper, we report a case of a patient with progressive muscle weakness carrying a novel heterozygous variant in the ISCU. Presence of other exonic or deep intronic variants was excluded. Although the phenotype is reminiscent of a recessive disease, studies performed in yeast Saccharomyces cerevisiae not only confirm a pathogenetic effect of the variant but also support its dominant inheritance.

Methods

Genetic studies

Whole exome sequencing (WES) was performed on the proband DNA (obtained from peripheral blood) using Twist Human Core Exome Plus Kit (Twist Bioscience) and sequenced with Illumina technology (100x depth of mean coverage). Reads were aligned to the hg38 reference genome. Obtained QC value was <99% for Q30. Alignment and variant calling were performed with an in-house bioinformatics pipeline. Identified variants were annotated using the Ensembl VEP as well as multiple databases, including dbSNP, dbNSFP, gnomAD, ClinVar, and HGMD. XHMMv1.0 algorithm and in-house scripts were used to search for small, rare CNVs. American College of Medical Genetics and Genomics (ACMG) Standards and Guidelines for the interpretation of sequence variants were followed in this study. Standard Sanger sequencing was performed to confirm the presence of the identified variant in the proband and to assess segregation in the family.

Yeast studies

The yeast strain used in this work, derived from W303-1B (Matα ade2-1 leu2-3, ura3-1 trp1-1 his3-11, 15 can1-100), is deleted at both ISU1 and ISU2 loci and expresses a wild type copy of ISU1 gene cloned in the URA3 bearing vector pFL38 to allow viability (Legati et al., 2017). Synthetic complete medium (SC) [0.69% yeast nitrogen base without amino acids (FormediumTM, UK)] supplemented with 1 g/L drop-out mix according to Kaiser et al. (1994), except amino acids and bases necessary to keep plasmids, was used to grow yeast strains. Media were supplemented with various carbon sources as indicated (Carlo Erba Reagents, Milan, Italy) in liquid phase or after solidification with 20 g/L agar (FormediumTM, UK). The human valine 134 residue corresponds to valine 135 in the yeast protein. The isu1^V135* mutant allele was generated by PCR QuikChange™ (Agilent) using KOD Hot Start DNA Polymerase (Merck), as template DNA the ISU1 cloned in the pFL39 plasmid (Legati et al., 2017) and the modified primers (base changes in bold) as follows: Isu1^V135*Fw 5′-GGA​GTT​GAG​CTT​GCC​CCC​ATA​AAA​GTT​GCA​TTG​CTC​TAT​GTT​AG-3′ and Isu1^V135*Rv 5′-CTA​ACA​TAG​AGC​AAT​GCA​ACT​TTT​ATG​GGG​GCA​AGC​TCA​ACT​CC-3’. After mutagenesis, sequence of the insert was verified by Sanger sequencing, and the pFL39isu1^V135* was used to transform the isu1∆isu2∆/pFL38ISU1 strain, using the lithium acetate method (Gietz and Schiestl, 2007). Transformants were selected for the presence of both constructs on solid SC medium lacking tryptophan and uracil. Yeast viability of isu1∆isu2∆ expressing isu1^V135* was evaluated by analysing the ability to grow on SC medium supplemented with 1 mg/mL 5- fluoroorotic acid (5-FOA) monohydrate (ForMedium) and 2% glucose as described in Cappuccio et al. (2021). Briefly, viability assays were performed by growing cells of two independent clones in liquid SC medium supplemented with uracil for 24 h until the early stationary phase to induce the loss of the plasmid carrying the wtISU1, and plating them (10-fold dilution spots starting from 4 × 10⁵ or 4 × 10⁴ cells/spot) in SC medium supplemented with 2% glucose, with or without 5-FOA. Results were scored after 72 h at 28°C.

For oxidative growth analysis, strains were serially diluted and spotted on SC-W agar plates, supplemented with 2% glycerol or 2% lactate or 2% glucose. The plates were incubated at 28°C. Cell yield was determined by growing cells on liquid medium containing glucose or glycerol and measuring the optical density at 600 nm after 72 h of growth at 28°C. Oxygen consumption rate (OCR) was measured by a Clark-type oxygen electrode (Oxygraph System Hansatech Instruments) (Figuccia et al., 2024) on whole cells grown in SC-W medium supplemented with 0.5% glucose until exhaustion for 18 h at 28°C.

Results

Clinical presentation

A 59-year-old patient (II:2) was referred to a Genetic Clinic (Institute of Psychiatry and Neurology in Warsaw, Poland) due to progressive weakness of hip and shoulder girdle muscles, which appeared around the age of 34. Physical examination revealed abnormal, unsteady gait, positive Gower`s sign, weakened tendon reflexes, great difficulty climbing and descending stairs. Periodic CK levels were normal. Muscle biopsy reported: “Small, uncharacteristic changes: centrally located nuclei, myofibril defects, one circular fiber”. In the electrocardiogram (ECG) examination - sinus rhythm, regular, normogram. Tandem MS/MS, lactic acid level in peripheral blood - no metabolic defects were found. Electromyography (EMG) has not been performed. Family history was negative. Limb girdle muscular dystrophy (LGMD) was suspected, and the patient underwent genetic testing. Myotonic dystrophy type 2 (MIM #602668) and a common pathogenic variant: c.550delA (NM_000070.3) in the CAPN3 gene were excluded.

Genetic studies

WES indicated a novel heterozygous variant c.399del (p.Val134Ter, exon 4) in the ISCU gene. Presence of a second exonic variant or deep intronic variants (including c.418 + 382 or IVS5+382G>C variant) were excluded. Presence of the c.399del variant was confirmed by Sanger sequencing in the proband (Supplementary Figure S1). No copy number variants (CNVs) were identified. The variant allele was not found in control chromosomes in the gnomAD (v3 and v4) database. The variant causes a premature termination of the protein. The variant is localized in the functional IscU_like domain of the ISCU protein (Figure 1A) with bioinformatics prediction of damaging effects on protein function. The variant affected a highly conserved residue throughout evolution (Figure 1B) and gave high scores of pathogenicity, according to several bioinformatics tools.

Figure 1

Figure 1. (A) Schematic representation of the ISCU gene, cDNA (NM_213595.4) and protein with the nucleotide/amino acid change identified in the Family (black) and literature (grey). The functional IscU-like domain is in yellow; the mitochondrial targeting sequence (MTS) is in green. (B) Multi-organism alignment. Human ISCU was aligned with ISC proteins from various organisms, including mammals, birds, amphibians, bony fishes, arthropods, nematodes, dicotyledon, fungi, and prokaryotes. The residue affect by mutation is highlighted in green, while Cys69, Cys95, and Cys138 which from part of the active site, are shown in yellow.

According to the ACMG guidelines (Richards et al., 2015), the c.399del (p.Val134Ter) in the ISCU gene is categorized to be “likely pathogenic variant”, because it belongs to PP1 (cosegregation with disease in multiple affected family members in a gene definitively known to cause the disease), PPP4 (patient’s phenotype and family history is highly specific for a disease with a single genetic etiology), PS3 (functional studies show damaging effect on the gene or gene product), PM2 (extremely low frequency in gnomAD population databases), and PM4 BP3 (protein length changes due to in-frame deletions/insertions and stop losses).

Clinical examination and genetics tests for the proband’s family were carried out (Figure 2 Pedigree).

Figure 2

Figure 2. Pedigree of the reported family. Black symbols designate affected subjects, and the arrow point to the index case. Genetic test (Sanger sequencing) for c.399del variant was performed for all family members except I:1, I:2 (DNA sample not available) and II:3.

Son 1 (III:2) was referred to a genetic clinic at the age of 37. Physical examination: no gait disturbances or significant muscle weakness. CK level–twice normal. Lactate level normal. He did not consent to the EMG examination. No familial variant in the ISCU was found.

Son 2 (III:3) was referred to a genetic clinic at the age of 32. Physical examination: no gait disturbances or significant muscle weakness, slight calves hypertrophy. CK level slightly elevated: 204.4 U/I (<190) and 376.2 U/L (<190.0), lactate level (peripheral blood) normal. He did not consent to the EMG examination. The presence of a familial variant: p.Val134Ter in the ISCU was confirmed.

The proband’s sister (II:1) was referred to a genetic clinic at the age of 77. Assessment of the musculoskeletal system during physical examination was difficult, the patient was bedbound, in the terminal stage of cancer. According to interview data, before the diagnosis of cancer, she walked with a cane and reported difficulties with walking since early adulthood. CK level, lactates, EMG were not performed due to lack of consent. The presence of the p.Val134Ter variant in the ISCU was confirmed.

Daughter of the sister of proband (III:1) was referred to a genetic clinic at the age of 58. Physical examination: no gait disturbances, no muscle weakness. The level of CK and lactates in peripheral blood was normal. No pathogenic variant was found in the ISCU.

Daughter of the daughter proband’s first sister (IV:1) was referred to a genetic clinic at the age of 37. Physical examination: no gait disturbances, no muscle weakness. The level of CK and lactates in peripheral blood was normal. No pathogenic variant was found in the ISCU.

In Table 1 resumed the clinical features of all patients described with ISCU variants.

Table 1

Table 1. Clinical characteristics of patients with ISCU variants.

Functional studies in yeast

To assess the pathogenicity of the novel p.Val134Ter ISCU variant, we performed complementation studies in Saccharomyces cerevisiae strain lacking the orthologous gene ISU1 and the paralogue ISU2, hereafter referred to as isu1Δisu2Δ, harbouring the centromeric pFL38 plasmid (URA3 marker) with the wild type (wt) ISU1 to allow viability (Legati et al., 2017). Since the p.Val134 residue is conserved between the two species, corresponding to p.Val135 in yeast, the change, equivalent to the human variant, was directly introduced into the yeast ISU1 wild type. The strain isu1Δisu2Δ/ISU1 was transformed with pFL39 centromeric plasmid (TRP1 marker) containing either the mutant allele isu1^V135*, a wt copy of ISU1, or no gene and the viability of the transformed strains was tested in medium supplemented with 5-FOA on which only cells which have lost wt ISU1 could grow. As shown in Figure 3A, the isu1^Val135* allele was unable to rescue the lethal phenotype of isu1Δisu2Δ since no growth was observed in 5-FOA indicating that isu1^Val135*behaves as null allele and confirming the pathogenicity of this variant.

Figure 3

Figure 3. Yeast functional analysis (A) Viability of isu1Δisu2Δ strains harbouring pFL38/ISU1 and transformed with wtISU1, or isu1^V135* mutant allele, cloned in pFL39, or pFL39 empty vector was evaluated by growth assays. Cell were grown on SC medium lacking tryptophan or both uracil and tryptophan, supplemented with 2% glucose, with or without 0.1% 5-FOA, at 28°C.Pictures were taken after 72 h. (B) Oxidative growth phenotype of the same strains as in (A) was evaluated in SC-U-W medium supplemented with the indicated carbon sources at 28°C. Ten-fold dilutions starting from 5 × 10⁴ cells/spot were spotted. Pictures were taken after 48 h. (C) Cell yield of the same strains described in (A) was calculated by growing cells on liquid SC-U-W medium containing glucose or glycerol at 28°C and measuring the optical density at 600 nm after 72 h. (D) Oxygen consumption rate (OCR) was carried out on the strains reported above grown in liquid SC-U-W medium supplemented with 0,5% of glucose at 28°C. Values are means ± standard deviation. *: p < 0.05 in One-Way ANOVA test with Bonferroni correction.

Yeast not only represents an excellent model system for investigating the role of novel variants in mitochondrial-related conditions but also a flexible tool also to assess the dominant or recessive nature of a mutation (Ceccatelli Berti et al., 2021). We then evaluated whether the Val135* mutation could act as a dominant trait. To this end we compared the growth phenotype of the heteroallelic strain isu1Δisu2Δ/ISU1/isu1^V135* with that of the homoallelic strain isu1Δisu2Δ/ISU1/ISU1 and the isu1Δisu2Δ/ISU1/hemiallelic one on both fermentable and non fermentable carbon sources. As shown in Figure 3A, on glucose containing medium no difference in fermentative growth was observed between the strains analysed. However, on medium containing glycerol or lactate, a condition in which the mitochondrial functionality is essential to obtain ATP, the growth of the heteroallelic strains shows a reduction, although slight, not only respect to that of the homoallelic strain, but also to that of the hemiallelic strain (Figure 3B).

In addition to the spot assay, to precisely and quantitatively evaluate the growth phenotype of mutant strains, not detectable with a semi-quantitative test such as a spot assay, a liquid-phase growth assay could be performed allowing the identification of minor defects. For this reason the mild reduction of oxidative growth displayed by the heteroallelic strain isu1Δisu2Δ/ISU1/isu1^V135* was better investigated by measuring the cell yield of the aforementioned strains in liquid medium. The result obtained confirmed what was observed in the previous analysis since the reduction was approximately 50% compared to both control strains (Figure 3C). Finally, oxygen consumption rate (OCR) can be measured to allow to determine the severity of the damage. Consistently, OCR was reduced by about 30% in the heteroallelic strain isu1Δisu2Δ/ISU1/isu1^V135* respect to both homoallelic and hemiallelic strain (Figure 3D). Together these results indicates that the Val135* mutation is dominant.

Discussion

Hereditary myopathy with lactic acidosis due to ISCU deficiency, also known as Swedish-type myopathy with exercise intolerance, is described as an autosomal recessive disorder. However, in this study, we presented the first family in which an autosomal dominant pattern of inheritance of ISCU-related myopathy has been identified. So far, only one sporadic case of ISCU-related myopathy caused by a mutation in a single allele of this gene has been described (Legati et al., 2017).

In the diagnostic process of our family, we used exome sequencing, which included CNV analysis and covered deep intron regions where known pathogenic variants are located. We identified a novel ISCU terminating variant c.399del in the exon 4, according to the MANE sequence. This change leads to the premature stop codon (p.Val134Ter) resulting in production of a shortened protein that is likely non-functional or/and possibly activates nonsense-mediated decay (NMD). Moreover, premature termination leads to the removal of one of three conserved cysteine residues (Cys183) in the active site of the enzyme, which could significantly impact protein function (Fox et al., 2019). It is known that the inability to express a full-length ISCU in humans results in Fe–S cluster deficiency (Tong and Rouault, 2000, Mochel et al., 2008; Tong and Rouault, 2006; Kollberg and Holme, 2009, Rawcliffe et al., 2018; Campbell et al., 2021). Furthermore, functional analysis has shown that suppression of human ISCU by RNAi not only inactivates mitochondrial and cytosolic aconitases, but also inappropriately activates the iron regulatory proteins thus disrupting intracellular iron homeostasis (Tiong and Rouault, 2006).

One of the best characterized ISCU variants is the deep intronic c.418 + 382G>C splice site mutation, detected in patients from northern Sweden. This change affects mRNA splicing and gives rise to the insertion of a pseudoexon between the last two exons in the mRNA sequence and to the introduction of a premature stop codon in the penultimate exon. This ultimately alters the C terminus of the protein and decreases levels of ISCU mRNA and protein in patients’ fibroblasts and lysates from skeletal muscle mitochondria (Mochel et al., 2008; Kollberg and Holme, 2009; Kollberg et al., 2009; Rawcliffe et al., 2018). Since the variant detected in our family is located in the penultimate exon, we suspect that it could have a similar effect.

Genetic segregation analysis and functional studies performed in the yeast Saccharomyces cerevisiae as a model system supported the dominant effect of the new identified variant and confirmed its gene–disease relationship. In particular, pedigree and clinical analyses have shown that the variant detected in the present work segregates with the symptoms of myopathy in various family members. Both our proband and her sister had great difficulty walking. One of the proband’s sons demonstrated mild calf enlargement, slightly elevated CK levels, and initial symptoms suggestive of developing myopathy. No increase in blood lactate levels were observed. Moreover, the symptoms of our proband were slightly different from those of the patient described by Legati et al., who mainly had distal muscle weakness, and whose phenotype was more reminiscent of the recessive disease. Our patient suffered in the first line from proximal muscle weakness, with periods of significant deterioration, and had a LGMD-like phenotype. Furthermore, CK level in our family ranged from normal to slightly elevated and no rhabdomyolysis was observed in any of them (Angelini, 1993). Due to the lack of EMG testing and muscle biopsy combined with biochemical tests in all family members, the myopathy phenotype is not fully defined. The further evaluation of the muscle biopsy was not possible and the other family members for the segregation were not available. Therefore, further clinical observation over time is required to better understand the progression of the disease.

In order to confirm the pathogenicity of the novel p.Val134Ter ISCU variant and to assess the dominant or recessive nature of this mutation we take advantage of the yeast ISCU model, i.e., a S. cerevisiae strain deleted in both ISU1and ISU2 genes and expressing the variant allele isu1^V135*and a wt copy of ISU1. The mutant allele was unable to complement the lethal phenotype of the null isu1Δisu2Δ double mutant thus confirming the complete loss of function of the truncated protein. Moreover, the oxidative growth phenotype of the heteroallelic strain isu1Δisu2Δ/ISU1/isu1^V135* has shown a slight defect referred to both the homoallelic and hemiallelic strains. This impairment of the oxidative metabolism was supported by the reduced respiratory rate in the ISCU model. These results indicate that the Val135Ter mutation is dominant and, since the phenotype of the heterozygous strain is more severe than that of the hemizygous strain, one can speculate that the mutation alone can be the cause of the pathology due to a negative dominance.

In the context of neuromuscular diseases, both recessive and dominant inheritance patterns for the same disease have been reported, with variable severity of clinical phenotypes within the families for the dominant variants, as seen in some LGMDs, such as calpainopathies (Angelini, 1993) or dysferlinopathies (Folland et al., 2022). It is known, also for mitochondrial diseases, that both recessive and dominant mutations in the same gene may lead to the same disease (Legati et al., 2017).

To date, only two pathogenic ISCU variants are reported in ClinVar: c.149G>A (p.Gly50Glu) located in the exon 4 and c.418 + 382G>C located in the intron region between exons 4 and 5. Approximately 60 variants are classified as variants of unknown significance (VUS). Some of them are associated with hereditary myopathy with lactic acidosis, however, functional evidence in ClinVar is missing for many of these variants.

This underscores the need for functional studies to better understand and characterize the effect of novel variants on protein function and metabolic pathways. In this regard, as this study also shows, yeast model once more proves to be a useful tool that can be used to assess the impact of VUS in a quick and efficient way (Ceccatelli Berti et al., 2021; Figuccia et al., 2024).

Our study confirms that a deep analysis of WES data is essential in the diagnosis process of genetic diseases. It should assume any mode of inheritance for genes directly related to the phenotype and/or condition. Although no specific therapy currently exists for ISCU-related myopathy, available evidence suggests that the disease correlates with a relatively normal lifespan. The disease has a chronic and progressive course with exacerbations and remissions. Further clinical and functional studies are needed to better understand the molecular mechanism and progression of the disease and to identify potential therapeutic approaches.

Data availability statement

Due to ethical and privacy considerations related to this brief study report, in which the analysis was based on WES data from a single patient followed by family analysis and functional studies, the datasets generated and/or analyzed during the current study (including VCF and BAM files) are not publicly available. However, they are available from the corresponding author upon reasonable request, provided that the request complies with applicable ethical approvals and data protection regulations.

Ethics statement

The studies involving humans were approved by Institute of Psychiatry and Neurology. The patient at the Institute of Psychiatry and Neurology signs an informed consent form for scientific research – the patients signed this form. Approval from the Bioethics Committee was not required because the biological sample taken from the patient (a blood sample) was part of the patient’s standard genetic diagnostics. Functional studies, on the other hand, were conducted using a yeast model without the participation of the patient or the use of any biological material collected from the patient. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

JR: Formal Analysis, Funding acquisition, Writing – original draft, Methodology, Investigation, Conceptualization. CCB: Conceptualization, Investigation, Funding acquisition, Methodology, Formal Analysis, Writing – original draft. DS: Writing – original draft, Investigation, Conceptualization. MB-M: Writing – review and editing. MM: Writing – review and editing. MK: Writing – review and editing, Supervision, Formal Analysis. AS-T: Formal Analysis, Writing – review and editing, Supervision. PG: Funding acquisition, Supervision, Conceptualization, Writing – review and editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This work has benefited from the equipment and framework of the COMP-HUB and COMP-R Initiatives, funded by the ‘Departments of Excellence’ program of the Italian Ministry for University and Research (MIUR, 2018-2022 and MUR, 2023-2027).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fgene.2025.1605440/full#supplementary-material

Supplementary Figure 1 | Electropherograms of the ISCU fragment showing the c.399del variant [NM_213595.4] in family members. The proband (II:2), the affected sibling (II:1), and the affected son (III:3) display a heterozygous variant (arrow), while the unaffected son (III:2) presents a wild-type sequence.

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