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miRNA-Coordinated Schizophrenia Risk Networks Cross-Talk with Cardiovascular Repair and Oppose Gliomagenesis

25 Pages Posted: 31 Jan 2019

See all articles by Hongbao Cao

Hongbao Cao

Shanxi Medical University

Ancha Baranova

George Mason University

Weihua Yue

Peking University - National Clinical Research Center for Mental Disorders

Hao Yu

Jining Medical University

Zufu Zhu

Southeast University (China)

Fuquan Zhang

Nanjing Medical University - Department of Psychiatry

Dongbai Liu

Southeast University (China) - Department of Neurology

More...

Abstract

Background: Schizophrenia risk genes are widely investigated, while systemic analysis of miRNA contributing to schizophrenia is lacking.

Methods: Schizophrenia-associated genetic loci profile was derived from genome-wide association study (GWAS) of Schizophrenia Working Group of the Psychiatric Genomics Consortium (PGC) dataset. Experimentally confirmed relationships between miRNAs and their target genes were retrieved from miRTarBase. Competitive gene set association analysis for miRNA-target regulations was conducted by the multi-marker analysis of genoMic annotation (MAGMA) and further validated by literature-based functional pathway analysis using Pathway Studio. The associations of the targets of three miRNAs with schizophrenia were further validated using a GWAS of antipsychotic treatment response.

Results: Three novel schizophrenia-risk miRNA, namely, miR-208b-3p, miR-208a-3p, and miR-494-5p and their targetomes converge on two calcium voltage-gated channel subunit alpha1 C (CACNA1C) and B-cell lymphoma 2 (Bcl-2), well-known as contributors to schizophrenia. Both miR-208a-3p and miR-208b-3p reduce expression of the RNA-binding protein Quaking (QKI), whose suppression commonly contributes to demyelinating model of schizophrenia and to ischemia/reperfusion injury. Both QKI and hsa-miR-494-5p simultaneously contribute to the risk of schizophrenia and serve as the inhibitors of gliomagenesis.

Conclusion: Presented results point at an orchestrating role of miRNAs in pathophysiology of schizophrenia. Cellular effects of risk-associated miRNAs align with the primary etiological hypotheses of schizophrenia. The sharing of regulatory networks schizophrenia and other pathologies may explain higher cardiovascular mortality and lower odds of gliomagenesis previously reported in psychiatric patients.

Funding Statement: The study was supported the National Natural Science Foundation of China (No. 81471364) and Primary Research & Development Plan of Jiangsu Province (BE2016630).

Declaration of Interests: The authors have nothing to disclose.

Ethics Approval Statement: Not applicable. All data were acquired from public databases that do not require an ethical approval.

Keywords: miRNA; schizophrenia; miR-208b-3p; miR-208a-3p; miR-494-5p; gliomagenesis; quaking

Suggested Citation

Cao, Hongbao and Baranova, Ancha and Yue, Weihua and Yu, Hao and Zhu, Zufu and Zhang, Fuquan and Liu, Dongbai, miRNA-Coordinated Schizophrenia Risk Networks Cross-Talk with Cardiovascular Repair and Oppose Gliomagenesis (November 1, 2019). Available at SSRN: https://ssrn.com/abstract=3315802

Hongbao Cao

Shanxi Medical University

Taiyuan, Shanxi
China

Ancha Baranova

George Mason University

4400 University Drive
Fairfax, VA 22030
United States

Weihua Yue

Peking University - National Clinical Research Center for Mental Disorders

No. 38 Xueyuan Road
Haidian District
Beijing, Beijing 100871
China

Hao Yu

Jining Medical University

Shenghua Rd
Jining
China

Zufu Zhu

Southeast University (China)

Sipailou 2#
Nanjing, Jiangsu Province 210096
China

Fuquan Zhang (Contact Author)

Nanjing Medical University - Department of Psychiatry ( email )

Wuxi, Jiangsu Province 214151
China

Dongbai Liu

Southeast University (China) - Department of Neurology ( email )

Jiangyin, Jiangsu Province 214431
China

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