Jilk R A, York D, Reznikoff W S
Department of Biochemistry, University of Wisconsin-Madison 53706, USA.
J Bacteriol. 1996 Mar;178(6):1671-9. doi: 10.1128/jb.178.6.1671-1679.1996.
The end sequences of the IS50 insertion sequence are known as the outside end (OE) and inside end. These complex ends are related but nonidentical 19-bp sequences that serve as substrates for the activity of the Tn5 transposase. Besides providing the binding site of the transposase, the end sequences of a transposon contain additional types of information necessary for transposition. These additional properties include but are not limited to host protein interaction sites and sites that program synapsis and cleavage events. In order to delineate the properties of the IS50 ends,the base pairs involved in the transposase binding site have been defined. This has been approached through performing a variety of in vitro analyses: a ++hydroxyl radical missing-nucleoside interference experiment, a dimethyl sulfate interference experiment, and an examination of the relative binding affinities of single-site end substitutions. These approaches have led to the conclusion that the transposase binds to two nonsymmetrical regions of the OE, including positions 6 to 9 and 13 to 19. Proper binding occurs along one face of the helix, over two major and minor grooves, and appears to result in a significant bending of the DNA centered approximately 3 bp from the donor DNA-OE junction.
IS50插入序列的末端序列被称为外侧末端(OE)和内侧末端。这些复杂的末端是相关但不相同的19个碱基对的序列,作为Tn5转座酶活性的底物。除了提供转座酶的结合位点外,转座子的末端序列还包含转座所需的其他类型信息。这些额外的特性包括但不限于宿主蛋白相互作用位点以及编程联会和切割事件的位点。为了描述IS50末端的特性,已经确定了转座酶结合位点中涉及的碱基对。这是通过进行各种体外分析来实现的:羟基自由基缺失核苷干扰实验、硫酸二甲酯干扰实验以及对单一位点末端取代的相对结合亲和力的研究。这些方法得出的结论是,转座酶与OE的两个非对称区域结合,包括第6至9位和第13至19位。正确的结合沿着螺旋的一个面发生,跨越两个大沟和小沟,并且似乎导致DNA在距供体DNA - OE连接处约3个碱基对处发生显著弯曲。