Blocking transcription through a nucleosome with synthetic DNA ligands

被引:83
作者
Gottesfeld, JM [1 ]
Belitsky, JM
Melander, C
Dervan, PB
Luger, K
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[2] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[3] Colorado State Univ, Dept Biochem & Mol Biol, Ft Collins, CO 80523 USA
关键词
nucleosome; transcription; pyrrole-imidazole polyamide;
D O I
10.1016/S0022-2836(02)00598-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pyrrole-imidazole (Py-Im) polyamides. are synthetic ligands that bind in the minor groove of DNA. Previous studies have established that sites on nucleosomal DNA facing away from the histone octamer, or even partially facing the histone octamer, are fully accessible for molecular recognition by Py-Im polyamides, and that nucleosomes remain fully folded upon ligand binding. Two polyamides that bind within the sea urchin 5 S gene nucleosome positioning sequence inhibit both heat-induced nucleosome sliding and transcription by bacteriophage T7 RNA polymerase from the nucleosomal template, but not from histone-free DNA. These polyamides prevent repositioning of the histone octamer by RNA polymerase, and thereby inhibit passage of the elongating polymerase through nucleosomal DNA. These results establish unambiguously the requirement for octamer mobility for transcription of nucleosomal templates by T7 RNA polymerase. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:249 / 263
页数:15
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