作者
Orna Issler,Yentl Y. van der Zee,Aarthi Ramakrishnan,Junshi Wang,Chunfeng Tan,Yong-Hwee E. Loh,Immanuel Purushothaman,Deena M. Walker,Zachary S. Lorsch,Peter J. Hamilton,Catherine Jensen Pena,Erin Flaherty,Brigham J. Hartley,Angélica Torres-Berrío,Eric M. Parise,Hope Kronman,Julia E. Duffy,Molly Estill,Erin S. Calipari,Benoit Labonté,Rachael L. Neve,Carol A. Tamminga,Kristen J. Brennand,Yan Dong,Li Shen,Eric J. Nestler
摘要
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.