Felippes Felipe F, Weigel Detlef
Department of Molecular Biology, Max Planck Institute for Developmental Biology, Spemannstrasse 35, 72076 Tübingen, Germany.
EMBO Rep. 2009 Mar;10(3):264-70. doi: 10.1038/embor.2008.247. Epub 2009 Jan 30.
Trans-acting small interfering RNAs (tasiRNAs) comprise a class of endogenous small RNAs that are generated from TAS gene-derived transcripts after these are cleaved at a microRNA (miRNA) target site. Arabidopsis thaliana has four families of TAS genes: miR173 triggers tasiRNA production from TAS1 and TAS2, miR390 from TAS3 and miR828 from TAS4. The two-hit trigger model postulates that dual target sites in the same transcript are often sufficient to initiate tasiRNA production, but two hits are not always required for tasiRNA formation. Here, we characterize the function of miR173 in the formation of tasiRNAs from TAS1 transcripts, as well as the importance of the TAS1 and TAS3 transcript sequences outside the miRNA-targeting sites for tasiRNA production. We show that tasiRNAs can be produced from heterologous transcripts containing miR173 or miR390 target sites, indicating that these trigger sequences are the only cis sequences essential for tasiRNA formation.
反式作用小干扰RNA(tasiRNA)是一类内源性小RNA,由TAS基因衍生的转录本在微小RNA(miRNA)靶位点被切割后产生。拟南芥有四个TAS基因家族:miR173触发TAS1和TAS2产生tasiRNA,miR390触发TAS3产生tasiRNA,miR828触发TAS4产生tasiRNA。双打击触发模型假定同一转录本中的双靶位点通常足以启动tasiRNA的产生,但tasiRNA的形成并不总是需要两次打击。在这里,我们描述了miR173在从TAS1转录本形成tasiRNA中的功能,以及TAS1和TAS3转录本中miRNA靶向位点之外的序列对于tasiRNA产生的重要性。我们表明,tasiRNA可以从含有miR173或miR390靶位点的异源转录本中产生,这表明这些触发序列是tasiRNA形成所必需的唯一顺式序列。