Journal Article

DZNE-2026-00453

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Estiar, M. A. ; Yu, E. ; Varghaei, P. ; Ross, J. P. ; Ashtiani, S. ; Bayne, A. N. ; Coarelli, G. ; Timmann, D. ; Klockgether, T.DZNE* ; Beijer, D.DZNE* ; Mengel, D.DZNE* ; Coutelier, M. ; Consortium, P. M. A. S. (Collaboration Author) ; Dion, P. A. ; Suchowersky, O. ; Ewenczyk, C. ; Goizet, C. ; Stevanin, G. ; Van Damme, P. ; Al-Chalabi, A. ; Zuchner, S. ; Synofzik, M.DZNE* ; Veldink, J. H. ; Trempe, J.-F. ; Durr, A. ; Rouleau, G. A. ; Gan-Or, Z.

2026
BioMed Central London

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Please use a persistent id in citations: doi:10.1186/s12916-026-04805-z

Abstract: Biallelic SPG7 mutations cause one of the most common forms of hereditary spastic paraplegia (HSP). Several reports have suggested that heterozygous SPG7 variants may also play a role in HSP, but also in amyotrophic lateral sclerosis (ALS). However, it remains controversial whether heterozygous SPG7 mutations are pathogenic on their own, or if other mechanisms are at play. We recently provided evidence for non-Mendelian inheritance in spastic paraplegia 7 (SPG7), as heterozygous carriers of SPG7 mutations often also carried mutations in other disease-related genes, including AFG3L2, more frequently than expected by chance. Given that SPG7 and AFG3L2 encode interacting subunits of the mitochondrial m-AAA protease complex, we hypothesized that combined heterozygous mutations in these genes may act synergistically to disrupt mitochondrial function and contribute to disease. In this study, we aimed to examine whether digenic heterozygous mutations in SPG7 and AFG3L2 can lead to a spectrum of neurodegenerative disorders.We first analyzed genome and exome sequencing data of 6644 unrelated individuals including 4817 motor neuron disorder (MND) and ataxia patients and 1827 controls. We next analyzed an additional 18,748 exome data from rare disease cohorts to further examine the occurrence of variants in SPG7 and AFG3L2.Among the first 4817 MND and ataxia patients, we identified a total of 6 patients, 4 of whom were unrelated, who carried potentially pathogenic variants in both SPG7 and AFG3L2, in contrast to none in 1827 unrelated controls. Further analysis of the 18,748 additional patients with rare disease, as well as a comprehensive literature review, identified 6 more patients, 5 of whom were unrelated, who had digenic mutations in SPG7 and AFG3L2. In the two families we identified, digenic mutations in SPG7 and AFG3L2 perfectly segregated with the disease. The 12 patients reported here exhibited predominant signs of motor neuron and cerebellar involvement.Our findings demonstrate that digenic inheritance of concurrent heterozygous mutations in SPG7 and AFG3L2 may cause motor neuron and cerebellar disorders. Screening of the entire SPG7 and AFG3L2 genes in genetically undiagnosed cases of MND and spastic ataxia may help to increase the diagnostic yield.

Keyword(s): Humans (MeSH) ; ATPases Associated with Diverse Cellular Activities: genetics (MeSH) ; Metalloendopeptidases: genetics (MeSH) ; Mutation (MeSH) ; Male (MeSH) ; Female (MeSH) ; ATP-Dependent Proteases: genetics (MeSH) ; Spastic Paraplegia, Hereditary: genetics (MeSH) ; Motor Neuron Disease: genetics (MeSH) ; Middle Aged (MeSH) ; Adult (MeSH) ; Cerebellar Diseases: genetics (MeSH) ; Heterozygote (MeSH) ; AFG3L2 ; Ataxia ; Cerebellar disorder ; Lateral sclerosis ; Motor neuron disorder ; SPG7 ; SPG7 protein, human ; ATPases Associated with Diverse Cellular Activities ; AFG3L2 protein, human ; Metalloendopeptidases ; ATP-Dependent Proteases

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Contributing Institute(s):

1. Patient Studies (Bonn) (Patient Studies (Bonn))
2. Parkinson Genetics (AG Gasser)

Research Program(s):

1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Appears in the scientific report 2026

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