Dynamic regulation of Z-DNA in the mouse prefrontal cortex by the RNA-editing enzyme Adar1 is required for fear extinction

Nat Neurosci. 2020 Jun;23(6):718-729. doi: 10.1038/s41593-020-0627-5. Epub 2020 May 4.

Abstract

DNA forms conformational states beyond the right-handed double helix; however, the functional relevance of these noncanonical structures in the brain remains unknown. Here we show that, in the prefrontal cortex of mice, the formation of one such structure, Z-DNA, is involved in the regulation of extinction memory. Z-DNA is formed during fear learning and reduced during extinction learning, which is mediated, in part, by a direct interaction between Z-DNA and the RNA-editing enzyme Adar1. Adar1 binds to Z-DNA during fear extinction learning, which leads to a reduction in Z-DNA at sites where Adar1 is recruited. Knockdown of Adar1 leads to an inability to modify a previously acquired fear memory and blocks activity-dependent changes in DNA structure and RNA state-effects that are fully rescued by the introduction of full-length Adar1. These findings suggest a new mechanism of learning-induced gene regulation that is dependent on proteins that recognize alternate DNA structure states, which are required for memory flexibility.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Deaminase / metabolism*
  • Adenosine Deaminase / physiology*
  • Animals
  • DNA, Z-Form / metabolism
  • DNA, Z-Form / physiology*
  • Extinction, Psychological / physiology*
  • Fear
  • Learning / physiology
  • Mice
  • Prefrontal Cortex / metabolism
  • RNA Editing / physiology*
  • RNA, Small Interfering / pharmacology

Substances

  • DNA, Z-Form
  • RNA, Small Interfering
  • ADAR1 protein, mouse
  • Adenosine Deaminase