Article | Published:

A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans

Genetics in Medicinevolume 20pages10041012 (2018) | Download Citation

Subjects

Abstract

Purpose

We aimed to identify the cause of disease in patients suffering from a distinctive, atypical form of Usher syndrome.

Methods

Whole-exome and genome sequencing were performed in five patients from three families of Yemenite Jewish origin, suffering from distinctive retinal degeneration phenotype and sensorineural hearing loss. Functional analysis of the wild-type and mutant proteins was performed in human fibrosarcoma cells.

Results

We identified a homozygous founder missense variant, c.133G>T (p.D45Y) in arylsulfatase G (ARSG). All patients shared a distinctive retinal phenotype with ring-shaped atrophy along the arcades engirdling the fovea, resulting in ring scotoma. In addition, patients developed moderate to severe sensorineural hearing loss. Both vision and hearing loss appeared around the age of 40 years. The identified variant affected a fully conserved amino acid that is part of the catalytic site of the enzyme. Functional analysis of the wild-type and mutant proteins showed no basal activity of p.D45Y.

Conclusion

Homozygosity for ARSG-p.D45Y in humans leads to protein dysfunction, causing an atypical combination of late-onset Usher syndrome. Although there is no evidence for generalized clinical manifestations of lysosomal storage diseases in this set of patients, we cannot rule out the possibility that mild and late-onset symptoms may appear.

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This study was financially supported by the Foundation Fighting Blindness USA (BR-GE-0214-0639 to D.S., E.B., and T.B.-Y.), Israel Science Foundation (2154/15 to S.K.), Chief Scientist Office of the Israeli Ministry of Health and the Lirot association (300009177 to S.K. and 300011893 to D.S. and T.B.-Y.), the Yedidut Research Grant (to E.B.), the Deutsche Forschungsgemeinschaft (DI 575/10-1 to T.D.), and the Swiss National Science Foundation (156260 to C.R.). The authors thank all patients and family members for their participation in this study, and Torben Lübke for critically reading the manuscript. Geto Mengisto, Kerstin Fentker and Mai-Britt Ilse, Inbar Erdinest, and Devora Marks-Ohana are acknowledged for expert technical assistance.

Author information

Affiliations

  1. Department of Ophthalmology, Hadassah–Hebrew University Medical Center, Jerusalem, Israel

    • Samer Khateb MD, PhD
    • , Netta Pollack BSc
    • , Alexey Obolensky PhD
    • , Eyal Banin MD, PhD
    •  & Dror Sharon PhD
  2. Department of Chemistry, Biochemistry I, Bielefeld University, Bielefeld, Germany

    • Björn Kowalewski PhD
    •  & Thomas Dierks PhD
  3. Department of Computational Biology, Unit of Medical Genetics, University of Lausanne, Lausanne, Switzerland

    • Nicola Bedoni MSc
    •  & Carlo Rivolta PhD
  4. Department of Biochemistry, University of Kiel, Kiel, Germany

    • Markus Damme PhD
  5. Monique and Jacques Roboh Department of Genetic Research and the Department of Genetic and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

    • Ann Saada PhD
  6. Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel

    • Tamar Ben-Yosef PhD
  7. Department of Otolaryngology—Head and Neck Surgery, Hadassah–Hebrew University Medical Center, Jerusalem, Israel

    • Menachem Gross MD
  8. Department of Genetics and Genome Biology, University of Leicester, Leicester, UK

    • Carlo Rivolta PhD

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Disclosure

The authors declare no conflict of interest

Corresponding authors

Correspondence to Thomas Dierks PhD or Eyal Banin MD, PhD or Carlo Rivolta PhD or Dror Sharon PhD.

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DOI

https://doi.org/10.1038/gim.2017.227