Kim Young-Kook, Kim V Narry
Department of Biological Sciences and Institute of Molecular Biology and Genetics, Seoul National University, Seoul, Korea.
EMBO J. 2007 Feb 7;26(3):775-83. doi: 10.1038/sj.emboj.7601512. Epub 2007 Jan 25.
The majority of human microRNA (miRNA) loci are located within intronic regions and are transcribed by RNA polymerase II as part of their hosting transcription units. The primary transcripts are cleaved by Drosha to release approximately 70 nt pre-miRNAs that are subsequently processed by Dicer to generate mature approximately 22 nt miRNAs. It is generally believed that intronic miRNAs are released by Drosha from excised introns after the splicing reaction has occurred. However, our database searches and experiments indicate that intronic miRNAs can be processed from unspliced intronic regions before splicing catalysis. Intriguingly, cleavage of an intron by Drosha does not significantly affect the production of mature mRNA, suggesting that a continuous intron may not be required for splicing and that the exons may be tethered to each other. Hence, Drosha may cleave intronic miRNAs between the splicing commitment step and the excision step, thereby ensuring both miRNA biogenesis and protein synthesis from a single primary transcript. Our study provides a novel example of eukaryotic gene organization and RNA-processing control.
大多数人类微小RNA(miRNA)基因座位于内含子区域,由RNA聚合酶II转录,作为其宿主转录单元的一部分。初级转录本被Drosha切割以释放约70个核苷酸的前体miRNA,随后Dicer对其进行加工以生成约22个核苷酸的成熟miRNA。一般认为,内含子miRNA是在剪接反应发生后由Drosha从切除的内含子中释放出来的。然而,我们的数据库搜索和实验表明,内含子miRNA可以在剪接催化之前从未剪接的内含子区域加工而来。有趣的是,Drosha对内含子的切割不会显著影响成熟mRNA的产生,这表明剪接可能不需要连续的内含子,外显子可能相互连接。因此,Drosha可能在剪接承诺步骤和切除步骤之间切割内含子miRNA,从而确保从单个初级转录本同时进行miRNA生物合成和蛋白质合成。我们的研究提供了一个真核基因组织和RNA加工控制的新例子。