MicroRNAs in the Onset of Schizophrenia

• Published in: Cells (Basel, Switzerland) Vol. 10; no. 10; p. 2679
• Main Authors: Thomas, Kristen T., Zakharenko, Stanislav S.
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 06.10.2021; MDPI
• Subjects: adolescence; Adolescents; Adults; Age; age of onset; Aging - genetics; Animal models; Animals; Base Sequence; Binding sites; Biosynthesis; Brain; Child development; Critical period; Gene Expression Regulation; Genes; Genetic Variation; Health risk assessment; Hemizygosity; Human subjects; Humans; Mental disorders; microRNA; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miR-29; miRNA; Neurodevelopment; Neurodevelopmental disorders; Protein biosynthesis; Proteins; Psychosis; Puberty; Review; Schizophrenia; Schizophrenia - genetics; Single-nucleotide polymorphism; Time Factors; 22q11.2 deletion syndrome; miR-132-3p; miR-137; miR-29; neurodevelopment; adolescence; DGCR8; microRNA; schizophrenia; age of onset
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells10102679

Mounting evidence implicates microRNAs (miRNAs) in the pathology of schizophrenia. These small noncoding RNAs bind to mRNAs containing complementary sequences and promote their degradation and/or inhibit protein synthesis. A single miRNA may have hundreds of targets, and miRNA targets are overrepresented among schizophrenia-risk genes. Although schizophrenia is a neurodevelopmental disorder, symptoms usually do not appear until adolescence, and most patients do not receive a schizophrenia diagnosis until late adolescence or early adulthood. However, few studies have examined miRNAs during this critical period. First, we examine evidence that the miRNA pathway is dynamic throughout adolescence and adulthood and that miRNAs regulate processes critical to late neurodevelopment that are aberrant in patients with schizophrenia. Next, we examine evidence implicating miRNAs in the conversion to psychosis, including a schizophrenia-associated single nucleotide polymorphism in MIR137HG that is among the strongest known predictors of age of onset in patients with schizophrenia. Finally, we examine how hemizygosity for DGCR8, which encodes an obligate component of the complex that synthesizes miRNA precursors, may contribute to the onset of psychosis in patients with 22q11.2 microdeletions and how animal models of this disorder can help us understand the many roles of miRNAs in the onset of schizophrenia.