MCM3AP and POMP mutations cause a DNA-repair and DNA-damage-signaling defect in an immunodeficient child

Research output: Contribution to journalArticlepeer-review

Authors

  • Daniela Salles
  • Eva-Maria Jacobsen
  • Thilo Dörk
  • Tobias Rausch
  • Sevtap Aydin
  • Harald Surowy
  • Meta Volcic
  • Walther Vogel
  • Klaus-Michael Debatin
  • Adrian M. Stütz
  • Klaus Schwarz
  • Ulrich Pannicke
  • Timo Hess
  • Jan O. Korbel
  • Ansgar S. Schulz
  • Johannes Schumacher
  • Lisa Wiesmüller

Colleges, School and Institutes

Abstract

Immunodeficiency patients with DNA repair defects exhibit radiosensitivity and proneness to leukemia/lymphoma formation. Though progress has been made in identifying the underlying mutations, in most patients the genetic basis is unknown. Two de novo mutated candidate genes, MCM3AP encoding germinal center‐associated nuclear protein (GANP) and POMP encoding proteasome maturation protein (POMP), were identified by whole‐exome sequencing (WES) and confirmed by Sanger sequencing in a child with complex phenotype displaying immunodeficiency, genomic instability, skin changes, and myelodysplasia. GANP was previously described to promote B‐cell maturation by nuclear targeting of activation‐induced cytidine deaminase (AID) and to control AID‐dependent hyperrecombination. POMP is required for 20S proteasome assembly and, thus, for efficient NF‐κB signaling. Patient‐derived cells were characterized by impaired homologous recombination, moderate radio‐ and cross‐linker sensitivity associated with accumulation of damage, impaired DNA damage‐induced NF‐κB signaling, and reduced nuclear AID levels. Complementation by wild‐type (WT)‐GANP normalized DNA repair and WT‐POMP rescued defective NF‐κB signaling. In conclusion, we identified for the first time mutations in MCM3AP and POMP in an immunodeficiency patient. These mutations lead to cooperative effects on DNA recombination and damage signaling. Digenic/polygenic mutations may constitute a novel genetic basis in immunodeficiency patients with DNA repair defects.

Details

Original languageEnglish
Pages (from-to)257-268
Number of pages12
JournalHuman Mutation
Volume37
Issue number3
Early online date30 Dec 2015
Publication statusPublished - Mar 2016

Keywords

  • Acetyltransferases/genetics, DNA Damage/genetics, DNA Repair/genetics, Humans, Immunologic Deficiency Syndromes/genetics, Intracellular Signaling Peptides and Proteins/genetics, Molecular Chaperones/genetics, Mutation/genetics, Signal Transduction/genetics