| Literature DB >> 32304628 |
Orna Issler1, Yentl Y van der Zee2, Aarthi Ramakrishnan1, Junshi Wang3, Chunfeng Tan4, Yong-Hwee E Loh1, Immanuel Purushothaman1, Deena M Walker1, Zachary S Lorsch1, Peter J Hamilton1, Catherine J Peña1, Erin Flaherty1, Brigham J Hartley1, Angélica Torres-Berrío1, Eric M Parise1, Hope Kronman1, Julia E Duffy1, Molly S Estill1, Erin S Calipari1, Benoit Labonté1, Rachael L Neve5, Carol A Tamminga4, Kristen J Brennand6, Yan Dong3, Li Shen1, Eric J Nestler7.
Abstract
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.Entities:
Keywords: CREB; depression; lncRNA; sex-differences
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Year: 2020 PMID: 32304628 PMCID: PMC7305959 DOI: 10.1016/j.neuron.2020.03.023
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173