Guil Sonia, Cáceres Javier F
Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh EH4 2XU, Scotland, UK.
Nat Struct Mol Biol. 2007 Jul;14(7):591-6. doi: 10.1038/nsmb1250. Epub 2007 Jun 10.
hnRNP A1 is an RNA-binding protein involved in various aspects of RNA processing. Use of an in vivo cross-linking and immunoprecipitation protocol to find hnRNP A1 RNA targets resulted in the identification of a microRNA (miRNA) precursor, pre-miR-18a. This microRNA is expressed as part of a cluster of intronic RNAs, including miR-17, miR-18a, miR-19a, miR-20a, miR-19b-1 and miR-92, and potentially acts as an oncogene. Here we show that hnRNP A1 binds specifically to the primary RNA sequence pri-miR-18a before Drosha processing. HeLa cells depleted of hnRNP A1 have reduced in vitro processing activity with pri-miR-18a and also show reduced abundances of endogenous pre-miR-18a. Furthermore, we show that hnRNP A1 is required for miR-18a-mediated repression of a target reporter in vivo. These results underscore a previously uncharacterized role for general RNA-binding proteins as auxiliary factors that facilitate the processing of specific miRNAs.
异质性核糖核蛋白A1(hnRNP A1)是一种参与RNA加工多个方面的RNA结合蛋白。使用体内交联和免疫沉淀方案来寻找hnRNP A1的RNA靶标,结果鉴定出一种微小RNA(miRNA)前体,即前体miR-18a。这种微小RNA作为一组内含子RNA的一部分表达,包括miR-17、miR-18a、miR-19a、miR-20a、miR-19b-1和miR-92,并可能作为一种癌基因发挥作用。在此我们表明,hnRNP A1在Drosha加工之前特异性结合初级RNA序列前体miR-18a。缺乏hnRNP A1的HeLa细胞对前体miR-18a的体外加工活性降低,并且内源性前体miR-18a的丰度也降低。此外,我们表明,体内miR-18a介导的靶标报告基因抑制需要hnRNP A1。这些结果强调了一般RNA结合蛋白作为促进特定miRNA加工的辅助因子的先前未被描述的作用。