Duval-Valentin G, Thuong N T, Hélène C
Laboratoire de Biophysique, Muséum National d'Histoire Naturelle, Institut National de la Santé et de la Recherche Médicale Unité 201, Centre National de la Recherche Scientifique, Paris, France.
Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):504-8. doi: 10.1073/pnas.89.2.504.
Homopyrimidine oligonucleotides bind to the major groove of a complementary homopyrimidine.homopurine stretch by triple helix formation. The bla gene from transposon Tn3 contains a homopyrimidine.homopurine sequence of 13 base pairs located just downstream of the RNA polymerase binding site. A 13-mer homopyrimidine oligonucleotide targeted to this sequence was tested for its effect on transcription of the bla gene in vitro. We show that the consequence of triple helix formation in front of the Escherichia coli RNA polymerase-promoter complex is to block the holoenzyme at its start site during a period that is dependent on temperature. The temperature dependence of transcription inhibition shows a direct correlation between this effect and the stabilization of the triple helix. Substitution of 5-methylcytosine to cytosine in the 13-mer oligonucleotide enhances triplex stability and transcription inhibition. Transcription inhibition by this synthetic repressor was also confirmed by footprinting studies demonstrating its specificity of action. The 13-mer oligonucleotide containing a psoralen derivative covalently linked to its 5' end shows an irreversible and specific inhibition of transcription initiation after exposure to light of wavelength greater than 310 nm.
同嘧啶寡核苷酸通过形成三链螺旋与互补的同嘧啶-同嘌呤序列的大沟结合。转座子Tn3的bla基因包含一个位于RNA聚合酶结合位点下游的13个碱基对的同嘧啶-同嘌呤序列。针对该序列的13聚体同嘧啶寡核苷酸在体外测试了其对bla基因转录的影响。我们表明,在大肠杆菌RNA聚合酶-启动子复合物前形成三链螺旋的结果是在依赖于温度的一段时间内将全酶阻断在其起始位点。转录抑制的温度依赖性表明这种效应与三链螺旋的稳定性之间存在直接相关性。在13聚体寡核苷酸中将5-甲基胞嘧啶替换为胞嘧啶可增强三链体稳定性和转录抑制。这种合成阻遏物的转录抑制也通过足迹研究得到证实,证明了其作用的特异性。在其5'端共价连接有补骨脂素衍生物的13聚体寡核苷酸在暴露于波长大于310nm的光后显示出对转录起始的不可逆和特异性抑制。