Aging and neurodegeneration are associated with increased mutations in single human neurons

Science. 2018 Feb 2;359(6375):555-559. doi: 10.1126/science.aao4426. Epub 2017 Dec 7.

Abstract

It has long been hypothesized that aging and neurodegeneration are associated with somatic mutation in neurons; however, methodological hurdles have prevented testing this hypothesis directly. We used single-cell whole-genome sequencing to perform genome-wide somatic single-nucleotide variant (sSNV) identification on DNA from 161 single neurons from the prefrontal cortex and hippocampus of 15 normal individuals (aged 4 months to 82 years), as well as 9 individuals affected by early-onset neurodegeneration due to genetic disorders of DNA repair (Cockayne syndrome and xeroderma pigmentosum). sSNVs increased approximately linearly with age in both areas (with a higher rate in hippocampus) and were more abundant in neurodegenerative disease. The accumulation of somatic mutations with age-which we term genosenium-shows age-related, region-related, and disease-related molecular signatures and may be important in other human age-associated conditions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Aging / genetics*
  • Child
  • Child, Preschool
  • Cockayne Syndrome / genetics
  • DNA Mutational Analysis
  • DNA Repair / genetics*
  • Female
  • Hippocampus / cytology
  • Hippocampus / embryology
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Mutation Rate*
  • Neurodegenerative Diseases / genetics*
  • Neurogenesis / genetics*
  • Neurons
  • Prefrontal Cortex / cytology
  • Prefrontal Cortex / embryology
  • Single-Cell Analysis
  • Whole Genome Sequencing
  • Xeroderma Pigmentosum / genetics
  • Young Adult