Schizophrenia is associated with an increase in cortical microRNA biogenesis

被引:335
作者
Beveridge, N. J. [1 ,2 ,3 ]
Gardiner, E. [1 ,2 ,3 ]
Carroll, A. P. [1 ,2 ,3 ]
Tooney, P. A. [1 ,2 ,3 ]
Cairns, M. J. [1 ,2 ,3 ]
机构
[1] Univ Newcastle, Sch Biomed Sci, Fac Hlth, Callaghan, NSW 2308, Australia
[2] Univ Newcastle, Hunter Med Res Inst, Callaghan, NSW 2308, Australia
[3] Schizophrenia Res Inst, Sydney, NSW, Australia
关键词
schizophrenia; microRNA; miRNA; DGCR8; dicer; GENE-EXPRESSION; PREFRONTAL CORTEX; MICROARRAY ANALYSIS; BIPOLAR DISORDER; TEMPORAL CORTEX; MESSENGER-RNA; BRAIN; REELIN; PROTEIN; HYPERMETHYLATION;
D O I
10.1038/mp.2009.84
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNA expression profiling and quantitative reverse transcription-PCR analysis of the superior temporal gyrus and the dorsolateral prefrontal cortex revealed a significant schizophrenia-associated increase in global microRNA expression. This change was associated with an elevation of primary microRNA processing and corresponded with an increase in the microprocessor component DGCR8. The biological implications for this extensive increase in gene silencing are profound, and were exemplified by members of the miR-15 family and other related microRNA, which were significantly upregulated in both brain regions. This functionally convergent influence is overrepresented in pathways involved in synaptic plasticity and includes many genes and pathways associated with schizophrenia, some of which were substantiated in vitro by reporter gene assay. Given the magnitude of microRNA changes and their wide sphere of influence, this phenomenon could represent an important dimension in the pathogenesis of schizophrenia. Molecular Psychiatry (2010) 15, 1176-1189; doi:10.1038/mp.2009.84; published online 1 September 2009
引用
收藏
页码:1176 / 1189
页数:14
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