Mencía Angeles, Modamio-Høybjør Silvia, Redshaw Nick, Morín Matías, Mayo-Merino Fernando, Olavarrieta Leticia, Aguirre Luis A, del Castillo Ignacio, Steel Karen P, Dalmay Tamas, Moreno Felipe, Moreno-Pelayo Miguel Angel
Unidad de Genética Molecular, Hospital Ramón y Cajal, Madrid, Spain.
Nat Genet. 2009 May;41(5):609-13. doi: 10.1038/ng.355. Epub 2009 Apr 12.
MicroRNAs (miRNAs) bind to complementary sites in their target mRNAs to mediate post-transcriptional repression, with the specificity of target recognition being crucially dependent on the miRNA seed region. Impaired miRNA target binding resulting from SNPs within mRNA target sites has been shown to lead to pathologies associated with dysregulated gene expression. However, no pathogenic mutations within the mature sequence of a miRNA have been reported so far. Here we show that point mutations in the seed region of miR-96, a miRNA expressed in hair cells of the inner ear, result in autosomal dominant, progressive hearing loss. This is the first study implicating a miRNA in a mendelian disorder. The identified mutations have a strong impact on miR-96 biogenesis and result in a significant reduction of mRNA targeting. We propose that these mutations alter the regulatory role of miR-96 in maintaining gene expression profiles in hair cells required for their normal function.
微小RNA(miRNA)通过与靶mRNA中的互补位点结合来介导转录后抑制,靶标识别的特异性关键取决于miRNA种子区域。已表明,mRNA靶位点内的单核苷酸多态性(SNP)导致的miRNA靶标结合受损会引发与基因表达失调相关的病理状况。然而,迄今为止,尚未报道过miRNA成熟序列内的致病突变。在此,我们表明,内耳毛细胞中表达的miRNA——miR-96种子区域的点突变会导致常染色体显性进行性听力损失。这是首次表明miRNA与孟德尔疾病相关的研究。所鉴定的突变对miR-96的生物合成有强烈影响,并导致mRNA靶向显著减少。我们认为,这些突变改变了miR-96在维持毛细胞正常功能所需的基因表达谱方面的调节作用。