Lee B L, Blake K R, Miller P S
Division of Biophysics, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, MD 21205.
Nucleic Acids Res. 1988 Nov 25;16(22):10681-97. doi: 10.1093/nar/16.22.10681.
The interaction of 4'-N(2-aminoethyl)aminomethyl-4,5',8-trimethylpsoralen-modified oligonucleoside methylphosphonates with synthetic ds-DNA containing a T7 RNA polymerase promoter was studied. The oligomers effectively crosslinked with either coding or noncoding ss-DNA when irradiated at 365 nm, but not with ds-DNA. The extent of the crosslinking reaction, which was complete within 16 min: (a) reached its maximum at an oligomer concentration of 3 microM; (b) remained constant below the Tm of the duplex and then rapidly decreased; and (c) appeared to depend upon the sequence surrounding the psoralen crosslinking site. An oligomer crosslinked to the template strand inhibited transcription by T7 RNA polymerase whereas an oligomer crosslinked to the non-template strand had only a small inhibitory effect. Oligomers did not crosslink to ds-DNA undergoing transcription nor did they inhibit the transcription reaction.
研究了4'-N(2-氨基乙基)氨甲基-4,5',8-三甲基补骨脂素修饰的寡核苷酸甲基膦酸酯与含有T7 RNA聚合酶启动子的合成双链DNA的相互作用。当在365nm处照射时,这些寡聚物能有效地与编码或非编码单链DNA发生交联,但不能与双链DNA交联。交联反应在16分钟内完成,其程度:(a)在寡聚物浓度为3μM时达到最大值;(b)在双链体的解链温度以下保持恒定,然后迅速下降;(c)似乎取决于补骨脂素交联位点周围的序列。与模板链交联的寡聚物抑制T7 RNA聚合酶的转录,而与非模板链交联的寡聚物只有很小的抑制作用。寡聚物不会与正在进行转录的双链DNA交联,也不会抑制转录反应。