Janowski Bethany A, Huffman Kenneth E, Schwartz Jacob C, Ram Rosalyn, Hardy Daniel, Shames David S, Minna John D, Corey David R
Department of Pharmacology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390, USA.
Nat Chem Biol. 2005 Sep;1(4):216-22. doi: 10.1038/nchembio725. Epub 2005 Jul 31.
Transcription start sites are critical switches for converting recognition of chromosomal DNA into active synthesis of RNA. Their functional importance suggests that they may be ideal targets for regulating gene expression. Here, we report potent inhibition of gene expression by antigene RNAs (agRNAs) complementary to transcription start sites within human chromosomal DNA. Silencing does not require methylation of DNA and differs from all known mechanisms for inhibiting transcription. agRNAs overlap DNA sequences within the open complex formed by RNA polymerase, and silencing is acutely sensitive to single base shifts. agRNAs effectively silence both TATA-less and TATA-box-containing promoters. Transcription start sites occur within every gene, providing predictable targets for agRNAs. Potent inhibition of multiple genes suggests that agRNAs may represent a natural mechanism for controlling transcription, may complement siRNAs and miRNAs that target mRNA, and will be valuable agents for silencing gene expression.
转录起始位点是将对染色体DNA的识别转化为RNA活性合成的关键开关。它们的功能重要性表明,它们可能是调节基因表达的理想靶点。在此,我们报告了与人类染色体DNA内转录起始位点互补的反基因RNA(agRNA)对基因表达的有效抑制。沉默不需要DNA甲基化,且不同于所有已知的抑制转录的机制。agRNA与RNA聚合酶形成的开放复合物内的DNA序列重叠,并且沉默对单碱基移位极为敏感。agRNA能有效沉默无TATA盒和含TATA盒的启动子。每个基因内都存在转录起始位点,为agRNA提供了可预测的靶点。对多个基因的有效抑制表明,agRNA可能代表了一种控制转录的天然机制,可能补充靶向mRNA的小干扰RNA(siRNA)和微小RNA(miRNA),并且将成为沉默基因表达的有价值工具。