Gottesfeld J M, Neely L, Trauger J W, Baird E E, Dervan P B
Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Nature. 1997 May 8;387(6629):202-5. doi: 10.1038/387202a0.
Small molecules that target specific DNA sequences have the potential to control gene expression. Ligands designed for therapeutic application must bind any predetermined DNA sequence with high affinity and permeate living cells. Synthetic polyamides containing N-methylimidazole and N-methylpyrrole amino acids have an affinity and specificity for DNA comparable to naturally occurring DNA-binding proteins. We report here that an eight-ring polyamide targeted to a specific region of the transcription factor TFIIIA binding site interferes with 5S RNA gene expression in Xenopus kidney cells. Our results indicate that pyrrole-imidazole polyamides are cell-permeable and can inhibit the transcription of specific genes.
靶向特定DNA序列的小分子具有控制基因表达的潜力。设计用于治疗应用的配体必须以高亲和力结合任何预定的DNA序列并穿透活细胞。含有N-甲基咪唑和N-甲基吡咯氨基酸的合成聚酰胺对DNA的亲和力和特异性与天然存在的DNA结合蛋白相当。我们在此报告,靶向转录因子TFIIIA结合位点特定区域的八环聚酰胺会干扰非洲爪蟾肾细胞中的5S RNA基因表达。我们的结果表明,吡咯-咪唑聚酰胺具有细胞穿透性,并且可以抑制特定基因的转录。