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Cip1-interacting zinc finger protein (CDKN1A-interacting zinc finger protein 1) (Nuclear protein NP94) (Zinc finger protein 356) [LSFR1] [NP94] [ZNF356]


DNA damage and neurodegenerative phenotypes in aged Ciz1 null mice.

Cell-cycle dysfunction and faulty DNA repair are closely intertwined pathobiological processes that may contribute to several neurodegenerative disorders. CDKN1A interacting zinc finger protein 1 (CIZ1) plays a critical role in DNA replication and cell-cycle progression at the G1/S checkpoint. Germline or somatic variants in CIZ1 have been linked to several neural and extra-neural diseases. Recently, we showed that germline knockout of Ciz1 is associated with motor and hematological abnormalities in young adult mice. However, the effects of CIZ1 deficiency in much older mice may be more relevant to understanding age-related declines in cognitive and motor functioning and age-related neurologic disorders such as isolated dystonia and Alzheimer disease. Mouse embryonic fibroblasts from Ciz1 mice showed abnormal sensitivity to the effects of γ-irradiation with persistent DNA breaks, aberrant cell-cycle progression, and apoptosis. Aged (18-month-old) Ciz1 mice exhibited marked deficits in motor and cognitive functioning, and, in brain tissues, overt DNA damage, NF-κB upregulation, oxidative stress, vascular dysfunction, inflammation, and cell death. These findings indicate that the deleterious effects of CIZ1 deficiency become more pronounced with aging and suggest that defects of cell-cycle control and associated DNA repair pathways in postmitotic neurons could contribute to global neurologic decline in elderly human populations. Accordingly, the G1/S cell-cycle checkpoint and associated DNA repair pathways may be targets for the prevention and treatment of age-related neurodegenerative processes.

MeSH Terms

  • Aging
  • Animals
  • Apoptosis
  • Brain
  • Cell Cycle
  • Cells, Cultured
  • Cognition
  • Cognitive Aging
  • DNA Damage
  • DNA Repair
  • Female
  • Fibroblasts
  • Genes, cdc
  • Male
  • Mice
  • Molecular Targeted Therapy
  • NF-kappa B
  • Neurodegenerative Diseases
  • Nuclear Proteins
  • Oxidative Stress
  • Phenotype


  • Aging
  • Apoptosis
  • CIZ1
  • Cell cycle
  • DNA damage