Blow Matthew J, Grocock Russell J, van Dongen Stijn, Enright Anton J, Dicks Ed, Futreal P Andrew, Wooster Richard, Stratton Michael R
Cancer Genome Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
Genome Biol. 2006;7(4):R27. doi: 10.1186/gb-2006-7-4-r27. Epub 2006 Apr 4.
MicroRNAs (miRNAs) are short RNAs of around 22 nucleotides that regulate gene expression. The primary transcripts of miRNAs contain double-stranded RNA and are therefore potential substrates for adenosine to inosine (A-to-I) RNA editing.
We have conducted a survey of RNA editing of miRNAs from ten human tissues by sequence comparison of PCR products derived from matched genomic DNA and total cDNA from the same individual. Six out of 99 (6%) miRNA transcripts from which data were obtained were subject to A-to-I editing in at least one tissue. Four out of seven edited adenosines were in the mature miRNA and were predicted to change the target sites in 3' untranslated regions. For a further six miRNAs, we identified A-to-I editing of transcripts derived from the opposite strand of the genome to the annotated miRNA. These miRNAs may have been annotated to the wrong genomic strand.
Our results indicate that RNA editing increases the diversity of miRNAs and their targets, and hence may modulate miRNA function.
微小RNA(miRNA)是一类长度约为22个核苷酸的短RNA,可调控基因表达。miRNA的初级转录本包含双链RNA,因此是腺苷到次黄苷(A-to-I)RNA编辑的潜在底物。
我们通过对来自同一个体的匹配基因组DNA和总cDNA的PCR产物进行序列比较,对十种人类组织中的miRNA的RNA编辑进行了调查。在获得数据的99个miRNA转录本中,有6个(6%)在至少一种组织中发生了A-to-I编辑。七个被编辑的腺苷中有四个位于成熟miRNA中,预计会改变3'非翻译区的靶位点。对于另外六个miRNA,我们鉴定出基因组中与注释的miRNA相反链的转录本发生了A-to-I编辑。这些miRNA可能被错误地注释到了错误的基因组链上。
我们的结果表明,RNA编辑增加了miRNA及其靶标的多样性,因此可能调节miRNA的功能。