The interaction of RELNDNMT genes involving in neurotrophin signaling pathway contributes to schizophrenia susceptibility

Author:

Ping Junjiao12,Wan Jing3,Luo Jiali2,Du Baoguo4,Liu Xinxia12,Jiang Tingyun1,Zhang Jie12ORCID

Affiliation:

1. Department of Psychiatry Third People's Hospital of Zhongshan City Zhongshan China

2. Joint Laboratory of Psychiatric Genetic Research The Third People's Hospital of Zhongshan Zhongshan China

3. Department of Early Intervention Third People's Hospital of Zhongshan City Zhongshan China

4. Department of Clinical Psychology The Third People's Hospital of Zhongshan City Zhongshan China

Abstract

AbstractObjectiveSchizophrenia belongs to a severe mental illness with complicated clinical presentations, an ill‐defined pathogenesis, and no known cause. Many genetic studies imply that polygenic interaction is important in the development of schizophrenia. The main mechanism of the RELN‐BDNF‐CREB‐DNMT signaling pathway in neurodevelopment involves RELN, brain‐derived neurotrophic factor (BDNF), transcription factor cyclic adenosine monophosphate response element binding protein (CREB), DNA methyltransferase 1 (DNMT1), as well as DNA methyltransferase 3B (DNMT3B). An early case–control research on 15 polymorphisms in the RELN, CREB, BDNF, DNMT1, and DNMT3B genes was done. A single gene variation has little effect on the pathogenesis of schizophrenia, but the combination of intergenic variation loci has a bigger impact because schizophrenia is a complex polygenic disorder. The objective of the current study sought to explore the impact of genetic interactions between RELN, BDNF, CREB, DNMT1, and DNMT3B on schizophrenia in order to further highlight the genetic factors influencing the risk of schizophrenia.MethodsTaking the case–control study design, with the Diagnostic and Statistical Manual of Mental Disorders‐Fifth Edition (DSM‐5) to be the evaluation norm, 134 individuals suffering from schizophrenia hospitalized in the Third People's Hospital of Zhongshan City within January 2018 to April 2020 (case group) were selected, and 64 healthy individuals (control group) from the same geographical area had been chosen as well. MassArray identified DNMT1 gene single nucleotide polymorphisms (rs2114724 and rs2228611) and DNMT3B gene SNPs (rs2424932, rs1569686, rs6119954, and rs2424908). Using the generalized multifactor dimensionality reduction (GMDR), the RELN‐BDNF‐CREB‐DNMT pathway's gene interactions were examined for their impact on schizophrenia.ResultsGMDR analysis showed that the three‐order interaction model RELN (rs2073559, rs2229864)–DNMT3B (rs2424908) was the optimal model (p = 0.001), with the consistency of cross‐validation of 10/10 and the test accuracy of 0.8711.ConclusionThe interaction between the RELN (rs2073559, rs2229864)–DNMT3B (rs2424908) may be related to schizophrenia, and large sample sizes should be verified in different population.

Funder

Medical Science and Technology Foundation of Guangdong Province

Zhongshan Science and Technology Bureau

Publisher

Wiley

Subject

Developmental Biology,Developmental Neuroscience

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