Integrating human endogenous retroviruses into transcriptome-wide association studies highlights novel risk factors for major psychiatric conditions.

TitleIntegrating human endogenous retroviruses into transcriptome-wide association studies highlights novel risk factors for major psychiatric conditions.
Publication TypeJournal Article
Year of Publication2024
AuthorsDuarte RRR, Pain O, Bendall ML, Rougvie Mde Mulder, Marston JL, Selvackadunco S, Troakes C, Leung SKay, Bamford RA, Mill J, O'Reilly PF, Srivastava DP, Nixon DF, Powell TR
JournalNat Commun
Volume15
Issue1
Pagination3803
Date Published2024 May 22
ISSN2041-1723
KeywordsAdult, Attention Deficit Disorder with Hyperactivity, Bipolar Disorder, Brain, Depressive Disorder, Major, Endogenous Retroviruses, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Mental Disorders, Risk Factors, Schizophrenia, Transcriptome
Abstract

Human endogenous retroviruses (HERVs) are repetitive elements previously implicated in major psychiatric conditions, but their role in aetiology remains unclear. Here, we perform specialised transcriptome-wide association studies that consider HERV expression quantified to precise genomic locations, using RNA sequencing and genetic data from 792 post-mortem brain samples. In Europeans, we identify 1238 HERVs with expression regulated in cis, of which 26 represent expression signals associated with psychiatric disorders, with ten being conditionally independent from neighbouring expression signals. Of these, five are additionally significant in fine-mapping analyses and thus are considered high confidence risk HERVs. These include two HERV expression signatures specific to schizophrenia risk, one shared between schizophrenia and bipolar disorder, and one specific to major depressive disorder. No robust signatures are identified for autism spectrum conditions or attention deficit hyperactivity disorder in Europeans, or for any psychiatric trait in other ancestries, although this is likely a result of relatively limited statistical power. Ultimately, our study highlights extensive HERV expression and regulation in the adult cortex, including in association with psychiatric disorder risk, therefore providing a rationale for exploring neurological HERV expression in complex neuropsychiatric traits.

DOI10.1038/s41467-024-48153-z
Alternate JournalNat Commun
PubMed ID38778015
PubMed Central IDPMC11111684
Grant ListR01 MH109897 / MH / NIMH NIH HHS / United States
R37 MH057881 / MH / NIMH NIH HHS / United States
R01 MH075916 / MH / NIMH NIH HHS / United States
U01 MH103392 / MH / NIMH NIH HHS / United States
R01 MH109677 / MH / NIMH NIH HHS / United States
R21 HG011513 / HG / NHGRI NIH HHS / United States
P50 MH084053 / MH / NIMH NIH HHS / United States
HHSN271201300031C / DA / NIDA NIH HHS / United States
R01 MH110921 / MH / NIMH NIH HHS / United States
P50 MH066392 / MH / NIMH NIH HHS / United States
R01 MH080405 / MH / NIMH NIH HHS / United States
R01 MH085542 / MH / NIMH NIH HHS / United States
R01 MH097276 / MH / NIMH NIH HHS / United States
P01 AG002219 / AG / NIA NIH HHS / United States
R01 MH093725 / MH / NIMH NIH HHS / United States
P50 AG005138 / AG / NIA NIH HHS / United States

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