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Allele-specific regulation of DISC1 expression by miR-135b-5p

机译:miR-135b-5p对DISC1表达的等位基因特异性调控

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Disrupted-in-schizophrenia-1 (DISC1) gene has been established as a risk factor for various neuropsychiatric phenotypes. Both coding and regulatory variants in DISC1 have been identified and associated with these phenotypes in genetic studies. MicroRNAs (miRNAs) are important regulators of protein coding genes. Since the miRNA-mRNA target recognition mechanism is vulnerable to disruption by DNA polymorphisms, we investigated whether polymorphisms in the DISC1 3andprime;UTR affect binding of miRNAs and lead to allele-specific regulation of DISC1. We identified four predicted polymorphic miRNA target sites in the DISC1 3andprime;UTR, and demonstrated that miR-135b-5p regulates the level of DISC1 mRNA. Moreover, DISC1 regulation by miR-135b-5p is allele specific: miR-135b-5p only binds to the major allele (A) of rs11122396, not to the minor allele (G). Thus, the G allele may be functionally related to the DISC1-associated phenotypes by abolishing regulation by miR-135b-5p, leading to elevated DISC1 levels.
机译:精神分裂症1(DISC1)基因已被确定为各种神经精神病学表型的危险因素。在遗传研究中,已识别出DISC1中的编码变体和调节变体,并将它们与这些表型相关联。微小RNA(miRNA)是蛋白质编码基因的重要调节剂。由于miRNA-mRNA目标识别机制易受DNA多态性的破坏,因此我们研究了DISC1 3和prime; UTR中的多态性是否影响miRNA的结合并导致DISC1的等位基因特异性调控。我们在DISC1 3和prime; UTR中鉴定了四个预测的多态性miRNA靶位点,并证明了miR-135b-5p调节DISC1 mRNA的水平。此外,miR-135b-5p对DISC1的调控是等位基因特异性的:miR-135b-5p仅与rs11122396的主要等位基因(A)结合,而与次要等位基因(G)结合。因此,通过取消miR-135b-5p的调节,可以导致G等位基因在功能上与DISC1相关的表型相关,从而导致DISC1水平升高。

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