4.8 Article

Sex-Specific Role for the Long Non-coding RNA LINC00473 in Depression

Journal

NEURON
Volume 106, Issue 6, Pages 912-+

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2020.03.023

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Funding

  1. National Institute of Mental Health (NIMH, USA) [R01MH51399, P50MH096890]
  2. Hope for Depression Research Foundation (HDRF, USA)
  3. Brain & Behavior Research Foundation (BBRF-NARSAD, USA)

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Depression is a common disorder that affects women at twice the rate of men. Here, we report that long non-coding RNAs (lncRNAs), a recently discovered class of regulatory transcripts, represent about one-third of the differentially expressed genes in the brains of depressed humans and display complex region- and sex-specific patterns of regulation. We identified the primate-specific, neuronal-enriched gene LINC00473 as downregulated in prefrontal cortex (PFC) of depressed females but not males. Using viral-mediated gene transfer to express LINC00473 in adult mouse PFC neurons, we mirrored the human sex-specific phenotype by inducing stress resilience solely in female mice. This sex-specific phenotype was accompanied by changes in synaptic function and gene expression selectively in female mice and, along with studies of human neuron-like cells in culture, implicates LINC00473 as a CREB effector Together, our studies identify LINC00473 as a female-specific driver of stress resilience that is aberrant in female depression.

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