Gralla J D
Proc Natl Acad Sci U S A. 1985 May;82(10):3078-81. doi: 10.1073/pnas.82.10.3078.
A DNase protection technique is described and applied to the interaction of three lac control proteins with supercoiled lac DNA. The technique uses end-labeled oligonucleotide primers to probe specific DNA regions as an alternative to protocols requiring restriction endonuclease cleavage or blotting. Thus DNA may be probed with high resolution in its native state. It is demonstrated that the introduction of supercoiling into DNA accelerates the rate of lac ps promoter binding by RNA polymerase but does not alter the positions at which polymerase, c-AMP-binding protein, or lac repressor bind to lac DNA.
本文描述了一种DNA酶保护技术,并将其应用于三种乳糖操纵子控制蛋白与超螺旋乳糖操纵子DNA的相互作用。该技术使用末端标记的寡核苷酸引物来探测特定的DNA区域,以此替代需要限制性内切酶切割或印迹的实验方案。因此,可以在天然状态下以高分辨率探测DNA。结果表明,将超螺旋引入DNA可加速RNA聚合酶与乳糖操纵子ps启动子的结合速率,但不会改变聚合酶、c-AMP结合蛋白或乳糖阻遏物与乳糖操纵子DNA结合的位置。