Ziegelbauer Joseph M, Sullivan Christopher S, Ganem Don
Howard Hughes Medical Institute, GW Hooper Foundation, University of California San Francisco, San Francisco, California 94143, USA.
Nat Genet. 2009 Jan;41(1):130-4. doi: 10.1038/ng.266. Epub 2008 Dec 21.
MicroRNAs (miRNAs) are short noncoding RNAs of cellular and viral origin that post-transcriptionally regulate gene expression through imperfect base pairing to their mRNA targets. Because the recognition sequences of miRNAs for their targets are short and may be discontinuous, bioinformatic prediction of targets is difficult. Here we present an approach to the experimental identification of the mRNA targets of miRNAs encoded by the Kaposi's sarcoma-associated herpesvirus (KSHV). KSHV encodes 17 miRNAs, derived from 12 pre-miRNAs expressed from a single locus during viral latency. We conducted multiple screens that examine small changes in transcript abundance under different conditions of miRNA expression or inhibition and then searched the identified transcripts for seed sequence matches. Using this strategy, we identified BCLAF1, encoding Bcl2-associated factor, as a target for miR-K5, and further analysis revealed that several other KSHV miRNAs also target this gene product. Our results support that this type of expression profiling provides a potentially general approach to the identification of miRNA targets.
微小RNA(miRNA)是细胞和病毒来源的短链非编码RNA,通过与mRNA靶标进行不完全碱基配对在转录后调控基因表达。由于miRNA与其靶标的识别序列较短且可能不连续,因此通过生物信息学预测靶标较为困难。在此,我们提出一种实验方法,用于鉴定卡波西肉瘤相关疱疹病毒(KSHV)编码的miRNA的mRNA靶标。KSHV编码17种miRNA,这些miRNA来源于病毒潜伏期间从单个位点表达的12个前体miRNA。我们进行了多次筛选,检测在miRNA表达或抑制的不同条件下转录本丰度的微小变化,然后在鉴定出的转录本中搜索种子序列匹配情况。使用这种策略,我们鉴定出编码Bcl2相关因子的BCLAF1作为miR-K5的靶标,进一步分析表明其他几种KSHV miRNA也靶向该基因产物。我们的结果支持这种类型的表达谱分析为鉴定miRNA靶标提供了一种潜在的通用方法。