Topoisomerase 3β knockout mice show transcriptional and behavioural impairments associated with neurogenesis and synaptic plasticity

Nat Commun. 2020 Jun 19;11(1):3143. doi: 10.1038/s41467-020-16884-4.

Abstract

Topoisomerase 3β (Top3β) is the only dual-activity topoisomerase in animals that can change topology for both DNA and RNA, and facilitate transcription on DNA and translation on mRNAs. Top3β mutations have been linked to schizophrenia, autism, epilepsy, and cognitive impairment. Here we show that Top3β knockout mice exhibit behavioural phenotypes related to psychiatric disorders and cognitive impairment. The mice also display impairments in hippocampal neurogenesis and synaptic plasticity. Notably, the brains of the mutant mice exhibit impaired global neuronal activity-dependent transcription in response to fear conditioning stress, and the affected genes include many with known neuronal functions. Our data suggest that Top3β is essential for normal brain function, and that defective neuronal activity-dependent transcription may be a mechanism by which Top3β deletion causes cognitive impairment and psychiatric disorders.

Publication types

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

MeSH terms

  • Animals
  • Behavior Observation Techniques
  • Behavior, Animal
  • Cognitive Dysfunction / diagnosis
  • Cognitive Dysfunction / genetics*
  • Cognitive Dysfunction / pathology
  • DNA Topoisomerases, Type I / genetics*
  • Disease Models, Animal
  • Female
  • Hippocampus / cytology
  • Hippocampus / diagnostic imaging
  • Hippocampus / growth & development
  • Hippocampus / pathology
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mental Disorders / diagnosis
  • Mental Disorders / genetics*
  • Mental Disorders / pathology
  • Mice
  • Mice, Knockout
  • Neurogenesis / genetics*
  • Neuronal Plasticity / genetics*
  • Neurons / pathology
  • Stereotaxic Techniques
  • Synaptic Potentials / genetics
  • Transcription, Genetic / physiology

Substances

  • Top3B protein, mouse
  • DNA Topoisomerases, Type I