Department of Biology, Stanford University, Stanford, CA 94305-5020, United States.
Department of Biology, Stanford University, Stanford, CA 94305-5020, United States.
Biochim Biophys Acta Gene Regul Mech. 2018 Feb;1861(2):158-166. doi: 10.1016/j.bbagrm.2017.12.008. Epub 2018 Jan 31.
The selective inhibition of transcription of a chosen gene by an artificial agent has numerous applications. Usually, these agents are designed to bind a specific nucleotide sequence in the promoter or within the transcribed region of the chosen gene. However, since optimal binding sites might not exist within the gene, it is of interest to explore the possibility of transcription inhibition when the agent is designed to bind at other locations. One of these possibilities arises when an additional transcription initiation site (e.g. secondary promoter) is present upstream from the primary promoter of the target gene. In this case, transcription inhibition might be achieved by inducing the formation of an RNA-DNA hybrid (R-loop) upon transcription from the secondary promoter. The R-loop could extend into the region of the primary promoter, to interfere with promoter recognition by RNA polymerase and thereby inhibit transcription. As a sequence-specific R-loop-inducing agent, a peptide nucleic acid (PNA) could be designed to facilitate R-loop formation by sequestering the non-template DNA strand. To investigate this mode for transcription inhibition, we have employed a model system in which a PNA binding site is localized between the T3 and T7 phage RNA polymerase promoters, which respectively assume the roles of primary and secondary promoters. In accord with our model, we have demonstrated that with PNA-bound DNA substrates, transcription from the T7 promoter reduces transcription from the T3 promoter by 30-fold, while in the absence of PNA binding there is no significant effect of T7 transcription upon T3 transcription.
人工试剂选择性抑制特定基因的转录具有许多应用。通常,这些试剂被设计用来结合所选基因启动子或转录区的特定核苷酸序列。然而,由于最佳结合位点可能不存在于基因内,因此探索当试剂被设计结合在其他位置时抑制转录的可能性是很有意义的。当目标基因的启动子上游存在额外的转录起始位点(例如二级启动子)时,就会出现这种可能性之一。在这种情况下,通过从二级启动子转录时诱导 RNA-DNA 杂交(R 环)的形成,可能会实现转录抑制。R 环可以延伸到启动子区域,干扰 RNA 聚合酶对启动子的识别,从而抑制转录。作为一种序列特异性的 R 环诱导剂,肽核酸(PNA)可以通过隔离非模板 DNA 链来促进 R 环的形成。为了研究这种转录抑制模式,我们采用了一种模型系统,其中 PNA 结合位点定位于 T3 和 T7 噬菌体 RNA 聚合酶启动子之间,它们分别充当主要和次要启动子的角色。与我们的模型一致,我们已经证明,在用 PNA 结合的 DNA 底物进行转录时,T7 启动子的转录使 T3 启动子的转录减少了 30 倍,而在没有 PNA 结合的情况下,T7 转录对 T3 转录没有显著影响。