Yansura D G, Goeddel D V, Cribbs D L, Caruthers M H
Nucleic Acids Res. 1977 Mar;4(3):723-37. doi: 10.1093/nar/4.3.723.
Chemically synthesized lactose operator DNA was tested for binding with lactose repressor protein. These operator DNAs were found to (1) bind specifically to lactose SQ repressor as measured by release of binding with the inducing ligand isopropyl-beta-D-thiogalactoside, (2) have dissociation half-lives of 37 seconds (21 base-paired duplex) and 46 seconds (26 base-paired duplex) and (3) have dissociation half-lives with x86 repressor of 9 minutes (21 base-paired duplex) and 18 minutes (26 base paired duplex). Modified operators containing 5-bromodeoxyuridine and deoxyuridine at specific sites were also prepared. These analogs bound both repressors about as tightly as the wild type sequence.
对化学合成的乳糖操纵基因DNA与乳糖阻遏蛋白的结合情况进行了测试。发现这些操纵基因DNA:(1)通过与诱导配体异丙基-β-D-硫代半乳糖苷结合的释放来衡量,能特异性地与乳糖SQ阻遏蛋白结合;(2)解离半衰期分别为37秒(21碱基对双链体)和46秒(26碱基对双链体);(3)与x86阻遏蛋白的解离半衰期分别为9分钟(21碱基对双链体)和18分钟(26碱基对双链体)。还制备了在特定位点含有5-溴脱氧尿苷和脱氧尿苷的修饰操纵基因。这些类似物与两种阻遏蛋白的结合紧密程度与野生型序列相近。