bioRxivGenomicsPreprint
Cell-Type-Specific Transcriptomic Signatures in Prefrontal Cortex Reveal lncRNA-mediated Gene Silencing and Enhancer Activities Contributing to the Pathophysiology of Major Depressive Disorder
Abstract
Long non-coding RNAs (lncRNAs) have emerged as pivotal epigenetic regulators that influence chromatin structure, gene expression, and various cellular processes. We conducted a comprehensive transcriptomic analysis to explore the regulatory roles of lncRNAs in gene expression across major cell types. Based on the cell type abundance as predicted by CIBERSORTx, the gene expression deconvolution of lncRNAs and mRNAs obtained from nonpsychiatric control (n=41) and MDD (n=59) subjects was carried out using bMIND. LncRNA regulatory activity and functional enrichment analysis were assessed in each cell type. Interactions between lncRNAs and transcription factors and RNA-binding proteins, as well as their associations with DNA and RNA, were obtained from the RNA Interactome Database. The protein-protein interactions of lncRNA-regulated mRNAs and the associations between genes and psychiatric disorders were sourced from STRING network PsyGeNET databases, respectively. We observed a prevalence of inhibitory neurons in the control group and a higher proportion of excitatory neurons within the MDD group. A significant dysregulation of lncRNAs and mRNAs, characterized by distinct gene-silencing activity of lncRNAs, was observed, potentially facilitated through chromatin modifications in excitatory and inhibitory neurons, as well as enhancer activity of specific lncRNAs in both neuronal and glial cell types. Functional analyses of the silenced neuronal genes highlighted the involvement of cell adhesion molecules and stress-related signaling in MDD, indicating disrupted neuron-glia interactions. The enhancer activity of lncRNAs indicated the positive regulation of genes involved in Hippo signaling and neurodegeneration. This work uniquely highlights the cell-type-specific roles of lncRNAs and their contributions to MDD pathophysiology. HIGHLIGHTSO_LIComprehensive cell-type-specific transcriptomic analysis of dorsolateral prefrontal cortex in MDD subjects. C_LIO_LIDistinct gene-silencing activity of lncRNAs in excitatory and inhibitory neurons. C_LIO_LIEnhancer activity of specific lncRNAs in both neuronal and glial cell types. C_LIO_LICritical roles of lncRNAs and associated cellular functions in the pathophysiology of MDD. C_LI
- organism: human
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- approach: benchmark study
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The Long Noncoding RNA FEDORA is a Cell-Type- and Sex-Specific Regulator of Depression
Orna Issler, Yentl Y. van der Zee, … Eric J. Nestler·Science AdvancesPeer-reviewed·Nov 30, 2022
- Cell type specific transcriptomic differences in depression show similar patterns between males and females but implicate distinct cell types and genes
Malosree Maitra, Haruka Mitsuhashi, … Corina Nagy·Nature CommunicationsPeer-reviewed·May 22, 2023
- Single-nucleus RNA sequencing shows convergent evidence from different cell types for altered synaptic plasticity in major depressive disorder.
Corina Nagy, Malosree Maitra, … Gustavo Turecki·Nature NeurosciencePeer-reviewed·Apr 27, 2020
- Dysregulation of Prefrontal Oligodendrocyte Lineage Cells Across Mouse Models of Adversity and Human Major Depressive Disorder
Sumeet K. Sharma, Wenjing Ma, … Zhaohui Steve Qin·bioRxiv·Mar 9, 2023
- LincRNAs involved in DCS-induced fear extinction: Shedding light on the transcriptomic dark matter
Stefanie Malan‐Müller, Vladimir B. C. de Souza, … Sian M. J. Hemmings·bioRxiv·Nov 8, 2019
- Overlapping yet distinct spatiomolecular profiles across mood disorders and biological sex in the human prefrontal cortex
Jacqueline R. Thompson, Seyun Oh, … Stephanie C. Page·bioRxiv·Oct 24, 2026