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LncRNA-AC006129.1 reactivates a SOCS3-mediated anti-inflammatory response through DNA methylation-mediated CIC downregulation in schizophrenia
Schizophrenia is a complex genetic disorder, the non-Mendelian features of which are likely complicated by epigenetic factors yet to be elucidated. Here, we performed RNA sequencing of peripheral blood RNA from monozygotic twins discordant for schizophrenia, and identified a schizophrenia-associated...
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Published in: | Molecular psychiatry 2021-08, Vol.26 (8), p.4511-4528 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Schizophrenia is a complex genetic disorder, the non-Mendelian features of which are likely complicated by epigenetic factors yet to be elucidated. Here, we performed RNA sequencing of peripheral blood RNA from monozygotic twins discordant for schizophrenia, and identified a schizophrenia-associated upregulated long noncoding RNA (lncRNA,
AC006129.1
) that participates in the inflammatory response by enhancing
SOCS3
and
CASP1
expression in schizophrenia patients and further validated this finding in
AC006129.1
-overexpressing mice showing schizophrenia-related abnormal behaviors. We find that
AC006129.1
binds to the promoter region of the transcriptional repressor Capicua (
CIC
), facilitates the interactions of DNA methyltransferases with the
CIC
promoter, and promotes DNA methylation-mediated CIC downregulation, thereby ameliorating CIC-induced
SOCS3
and
CASP1
repression. Derepression of
SOCS3
enhances the anti-inflammatory response by inhibiting JAK/STAT-signaling activation. Our findings reveal an epigenetic mechanism with etiological and therapeutic implications for schizophrenia. |
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ISSN: | 1359-4184 1476-5578 |
DOI: | 10.1038/s41380-020-0662-3 |