Megraw Molly, Baev Vesselin, Rusinov Ventsislav, Jensen Shane T, Kalantidis Kriton, Hatzigeorgiou Artemis G
Center for Bioinformatics and Department of Genetics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
RNA. 2006 Sep;12(9):1612-9. doi: 10.1261/rna.130506. Epub 2006 Aug 3.
In this study we present a method of identifying Arabidopsis miRNA promoter elements using known transcription factor binding motifs. We provide a comparative analysis of the representation of these elements in miRNA promoters, protein-coding gene promoters, and random genomic sequences. We report five transcription factor (TF) binding motifs that show evidence of overrepresentation in miRNA promoter regions relative to the promoter regions of protein-coding genes. This investigation is based on the analysis of 800-nucleotide regions upstream of 63 experimentally verified Transcription Start Sites (TSS) for miRNA primary transcripts in Arabidopsis. While the TATA-box binding motif was also previously reported by Xie and colleagues, the transcription factors AtMYC2, ARF, SORLREP3, and LFY are identified for the first time as overrepresented binding motifs in miRNA promoters.
在本研究中,我们提出了一种利用已知转录因子结合基序来鉴定拟南芥miRNA启动子元件的方法。我们对这些元件在miRNA启动子、蛋白质编码基因启动子和随机基因组序列中的表现进行了比较分析。我们报告了五个转录因子(TF)结合基序,相对于蛋白质编码基因的启动子区域,这些基序在miRNA启动子区域中显示出超量存在的证据。这项研究基于对拟南芥中63个经实验验证的miRNA初级转录本转录起始位点(TSS)上游800个核苷酸区域的分析。虽然谢及其同事之前也曾报道过TATA框结合基序,但转录因子AtMYC2、ARF、SORLREP3和LFY首次被鉴定为在miRNA启动子中超量存在的结合基序。