Literature DB >> 23378013

Maturation of the human dorsolateral prefrontal cortex coincides with a dynamic shift in microRNA expression.

Natalie J Beveridge1, Danielle M Santarelli, Xi Wang, Paul A Tooney, Maree J Webster, Cynthia S Weickert, Murray J Cairns.   

Abstract

MicroRNA are small RNAs that provide specificity for the RNA induced silencing complex, which forms the basis of an exquisite combinatorial system for posttranscriptional regulation. This system, essential for complex metazoans, is exemplified in the development of the cerebral cortex. To explore the complexity of human cortical miRNA expression in detail, we analyzed RNA from postmortem prefrontal cortex from 97 subjects aged 2 months to 78 years using miRNA microarray. Global miRNA expression was highest in the early years before declining significantly after adolescence (n = 140 decreased, n = 32 increased). Late adolescence was also marked by an inflection point between miRNA on an upward trajectory vs the majority going down. Functional annotation of target genes displaying inverse mRNA expression patterns in the same tissue were overrepresented in neurodevelopmentally significant pathways including neurological disease (most significantly schizophrenia), nervous system development, and cell-to-cell signaling. As mature miRNA expression is largely posttranscriptionally regulated, miRNA biogenesis gene expression was also examined. Dicer and Exportin-5 displayed significant associations with age; however, neither correlated with global miRNA expression across the lifespan. This investigation of cortical miRNA expression provides a framework for understanding the complex posttranscriptional regulatory environment during development and aging that may form a substrate for changes observed in neurodevelopmental disorders.

Entities:  

Keywords:  aging; ment; miRNA; neurodevelop‐; prefrontal cortex; schizophrenia

Mesh:

Substances:

Year:  2013        PMID: 23378013      PMCID: PMC3932079          DOI: 10.1093/schbul/sbs198

Source DB:  PubMed          Journal:  Schizophr Bull        ISSN: 0586-7614            Impact factor:   9.306


  52 in total

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5.  Development of cortical circuitry and cognitive function.

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6.  Developmental co-regulation of the beta and gamma GABAA receptor subunits with distinct alpha subunits in the human dorsolateral prefrontal cortex.

Authors:  Stu G Fillman; Carlotta E Duncan; Maree J Webster; Michael Elashoff; Cynthia Shannon Weickert
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7.  A MicroRNA feedback circuit in midbrain dopamine neurons.

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8.  Expression profiles of schizophrenia susceptibility genes during human prefrontal cortical development.

Authors:  Kwang H Choi; Megan E Zepp; Brandon W Higgs; Cynthia S Weickert; Maree J Webster
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9.  Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia.

Authors:  Nikolaos Mellios; Hsien-Sung Huang; Stephen P Baker; Marzena Galdzicka; Edward Ginns; Schahram Akbarian
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Authors:  Chi-Yu Lai; Sung-Liang Yu; Ming H Hsieh; Chun-Houh Chen; Hsuan-Yu Chen; Chun-Chiang Wen; Yung-Hsiang Huang; Po-Chang Hsiao; Chuhsing Kate Hsiao; Chih-Min Liu; Pan-Chyr Yang; Hai-Gwo Hwu; Wei J Chen
Journal:  PLoS One       Date:  2011-06-29       Impact factor: 3.240

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1.  Converging evidence implicates the abnormal microRNA system in schizophrenia.

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Journal:  Schizophr Bull       Date:  2014-11-26       Impact factor: 9.306

Review 2.  Altering the course of schizophrenia: progress and perspectives.

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5.  Reciprocal Alterations in Regulator of G Protein Signaling 4 and microRNA16 in Schizophrenia.

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6.  Transcriptome study of differential expression in schizophrenia.

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7.  MicroRNA Alterations in Induced Pluripotent Stem Cell-Derived Neurons from Bipolar Disorder Patients: Pathways Involved in Neuronal Differentiation, Axon Guidance, and Plasticity.

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9.  miR-936 is Increased in Schizophrenia and Inhibits Neural Development and AMPA Receptor-Mediated Synaptic Transmission.

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10.  The relationship between DNA methylation in neurotrophic genes and age as evidenced from three independent cohorts: differences by delirium status.

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Journal:  Neurobiol Aging       Date:  2020-06-12       Impact factor: 5.133

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