Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders. (2nd January 2021)

• Record Type: Journal Article
• Authors: Carmel, Miri; Michaelovsky, Elena; Weinberger, Ronnie; Frisch, Amos; Mekori-Domachevsky, Ehud; Gothelf, Doron; Weizman, Abraham
• Is Part Of: World journal of biological psychiatry. Volume 22:Number 1(2021)
• Page Start: 46
• Page End: 57
• Publication Date: 2021-01-02
• Subjects: Schizophrenia spectrum disorders -- 22q11.2 deletion syndrome -- epigenetics/DNA methylation -- imprinting genes -- MHC locus; Biological psychiatry -- Periodicals; Biological Psychiatry -- Periodicals; 616.89
• DOI: 10.1080/15622975.2020.1747113
• Languages: English
• ISSNs: 1562-2975

Abstract

Abstract: Objectives: 22q11.2 deletion syndrome (DS) is the strongest known genetic risk for schizophrenia. Methylome screening was conducted to elucidate possible involvement of epigenetic alterations in the emergence of schizophrenia spectrum disorders (SZ-SD) in 22q11.2DS. Methods: Sixteen adult men with/without SZ-SD were recruited from a 22q11.2DS cohort and underwent genome-wide DNA methylation profile analysis. Differentially methylated probes (DMPs) and regions (DMRs) were analysed using the ChAMP software. Results: The DMPs ( p -value <10 −6 ) and DMRs ( p -valueArea <0.01) were enriched in two gene sets, 'imprinting genes' and 'chr6p21', a region overlapping the MHC locus. Most of the identified imprinting genes are involved in neurodevelopment and located in clusters under imprinting control region (ICR) regulation, including PEG10, SGCE (7q21.3), GNAS, GNAS-AS1 (20q13.32) and SNHG14, SNURF-SNRPN, SNORD115 (15q11.2). The differentially methylated genes from the MHC locus included immune HLA -genes and non-immune genes, RNF39, PPP1R18 and NOTCH4, implicated in neurodevelopment and synaptic plasticity. The most significant DMR is located in MHC locus and covered the transcription regulator ZFP57 that is required for control and maintenance of gene imprinting at multiple ICRs. Conclusions: The differential methylation in imprinting genes and in chr6p21-22 indicate the neurodevelopmental nature of 22q11.2DS-related SZ and the major role of MHC locus in the risk to develop SZ.