Ichikawa H, Ikeda K, Wishart W L, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
Proc Natl Acad Sci U S A. 1987 Dec;84(23):8220-4. doi: 10.1073/pnas.84.23.8220.
Tn3 transposase, which is required for transposition of Tn3, has been purified by a low-ionic-strength-precipitation method. Using a nitrocellulose filter binding assay, we have shown that transposase binds to any restriction fragment. However, binding of the transposase to specific fragments containing the terminal inverted repeat sequences of Tn3 can be demonstrated by treatment of transposase-DNA complexes with heparin, which effectively removes the transposase bound to the other nonspecific fragments at pH 5-6. DNase I "footprinting" analysis showed that the transposase protects an inner 25-base-pair region of the 38-base-pair terminal inverted repeat sequence of Tn3. This protection is not dependent on pH. Interestingly, binding of the transposase to the inverted repeat sequences facilitates DNase I to nick at the end of the Tn3 sequence. It was also observed that the transposase protects the end regions of restriction fragments with a cohesive sequence at their 5' end or with a flush end from DNase I cleavage. The specific and nonspecific binding of transposase to DNA is ATP-independent.
Tn3转座酶是Tn3转座所必需的,已通过低离子强度沉淀法进行了纯化。使用硝酸纤维素滤膜结合试验,我们发现转座酶能与任何限制性片段结合。然而,通过用肝素处理转座酶-DNA复合物,可证明转座酶与含有Tn3末端反向重复序列的特定片段的结合,在pH 5-6时,肝素能有效去除与其他非特异性片段结合的转座酶。DNase I “足迹”分析表明,转座酶可保护Tn3 38个碱基对的末端反向重复序列内部的25个碱基对区域。这种保护不依赖于pH。有趣的是,转座酶与反向重复序列的结合促进了DNase I在Tn3序列末端的切口。还观察到,转座酶可保护5'端具有粘性序列或平端的限制性片段的末端区域不被DNase I切割。转座酶与DNA的特异性和非特异性结合不依赖于ATP。