Regulatory BC1 RNA in cognitive control

  1. Henri Tiedge1,2,4
  1. 1The Robert F. Furchgott Center for Neural and Behavioral Science, State University of New York Downstate Medical Center, Brooklyn, New York 11203, USA
  2. 2Department of Physiology and Pharmacology, State University of New York Downstate Medical Center, Brooklyn, New York 11203, USA
  3. 3Statistical Design and Analysis, Research Division, State University of New York Downstate Medical Center, Brooklyn, New York 11203, USA
  4. 4Department of Neurology, State University of New York Downstate Medical Center, Brooklyn, New York 11203, USA
  1. Corresponding author: henri.tiedge{at}downstate.edu
  • 5 Present address: Environmental Health & Safety, Columbia University Medical Center, New York, NY 10032, USA.

Abstract

Dendritic regulatory BC1 RNA is a non-protein-coding (npc) RNA that operates in the translational control of gene expression. The absence of BC1 RNA in BC1 knockout (KO) animals causes translational dysregulation that entails neuronal phenotypic alterations including prolonged epileptiform discharges, audiogenic seizure activity in vivo, and excessive cortical oscillations in the γ frequency band. Here we asked whether BC1 RNA control is also required for higher brain functions such as learning, memory, or cognition. To address this question, we used odor/object attentional set shifting tasks in which prefrontal cortical performance was assessed in a series of discrimination and conflict learning sessions. Results obtained in these behavioral trials indicate that BC1 KO animals were significantly impaired in their cognitive flexibility. When faced with conflicting information sources, BC1 KO animals committed regressive errors as they were compromised in their ability to disengage from recently acquired memories even though recall of such memories was in conflict with new situational context. The observed cognitive deficits are reminiscent of those previously described in subtypes of human autism spectrum disorders.

  • Received February 28, 2017.
  • Accepted April 12, 2017.

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