LncRNA-AC006129.1 reactivates a SOCS3-mediated anti-inflammatory response through DNA methylation-mediated CIC downregulation in schizophrenia

LncRNA-AC006129.1 通过 DNA 甲基化介导的精神分裂症 CIC 下调重新激活 SOCS3 介导的抗炎反应

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作者:Chaoying Ni #, Wei Jiang #, Zhongju Wang #, Zhuo Wang, Jian Zhang, Xianzhen Zheng, Zelin Liu, Haiyan Ou, Tingyun Jiang, Wenquan Liang, Fengchun Wu, Qiyang Li, Yu Hou, Qiong Yang, Bo Guo, Sihan Liu, Shuyun Li, Shufen Li, Ence Yang, Xin-Hong Zhu, Xingbing Huang, Zhexing Wen, Cunyou Zhao1

Abstract

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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