Borchert Glen M, Lanier William, Davidson Beverly L
Department of Internal Medicine, University of Iowa, Iowa City, Iowa 52242, USA.
Nat Struct Mol Biol. 2006 Dec;13(12):1097-101. doi: 10.1038/nsmb1167. Epub 2006 Nov 12.
Prior work demonstrates that mammalian microRNA (miRNA or miR) expression requires RNA polymerase II (Pol II). However, the transcriptional requirements of many miRNAs remain untested. Our genomic analysis of miRNAs in the human chromosome 19 miRNA cluster (C19MC) revealed that they are interspersed among Alu repeats. Because Alu transcription occurs through RNA Pol III recruitment, and we found that Alu elements upstream of C19MC miRNAs retain sequences important for Pol III activity, we tested the promoter requirements of C19MC miRNAs. Chromatin immunoprecipitation and cell-free transcription assays showed that Pol III, but not Pol II, is associated with miRNA genomic sequence and sufficient for transcription. Moreover, the mature miRNA sequences of approximately 50 additional human miRNAs lie within Alu and other known repetitive elements. These findings extend the current view of miRNA origins and the transcriptional machinery driving their expression.
先前的研究表明,哺乳动物微小RNA(miRNA或miR)的表达需要RNA聚合酶II(Pol II)。然而,许多miRNA的转录需求仍未得到验证。我们对人类19号染色体微小RNA簇(C19MC)中的miRNA进行的基因组分析表明,它们散布于Alu重复序列之间。由于Alu转录是通过招募RNA Pol III发生的,并且我们发现C19MC miRNAs上游的Alu元件保留了对Pol III活性至关重要的序列,因此我们测试了C19MC miRNAs的启动子需求。染色质免疫沉淀和无细胞转录分析表明,与miRNA基因组序列相关并足以进行转录的是Pol III,而非Pol II。此外,另外约50种人类miRNA的成熟miRNA序列位于Alu和其他已知的重复元件内。这些发现扩展了目前关于miRNA起源以及驱动其表达的转录机制的观点。