Yin Zhiqi, Jayaram Makkuni, Pathania Shailja, Harshey Rasika M
Section of Molecular Genetics and Microbiology and Institute of Cellular and Molecular Biology, University of Texas, Austin, TX 78712, USA.
J Biol Chem. 2005 Feb 18;280(7):6149-56. doi: 10.1074/jbc.M411679200. Epub 2004 Nov 24.
A Mu transpososome assembled on negatively supercoiled DNA traps five supercoils by intertwining the left (L) and right (R) ends of Mu with an enhancer element (E). To investigate the contribution of DNA supercoiling to this elaborate synapse in which E and L cross once, E and R twice, and L and R twice, we have analyzed DNA crossings in a transpososome assembled on nicked substrates under conditions that bypass the supercoiling requirement for transposition. We find that the transposase MuA can recreate an essentially similar topology on nicked substrates, interwrapping both E-R and L-R twice but being unable to generate the single E-L crossing. In addition, we deduce that the functional MuA tetramer must contribute to three of the four observed crossings and, thus, to restraining the enhancer within the complex. We discuss the contribution of both MuA and DNA supercoiling to the 5-noded Mu synapse built at the 3-way junction.
组装在负超螺旋 DNA 上的 Mu 转座体通过将 Mu 的左端(L)和右端(R)与增强子元件(E)缠绕在一起捕获五个超螺旋。为了研究 DNA 超螺旋对这种精细突触的贡献,其中 E 与 L 交叉一次,E 与 R 交叉两次,L 与 R 交叉两次,我们分析了在切口底物上组装的转座体中的 DNA 交叉,该条件绕过了转座对超螺旋的要求。我们发现转座酶 MuA 可以在切口底物上重新创建基本相似的拓扑结构,E-R 和 L-R 都缠绕两次,但无法产生单个 E-L 交叉。此外,我们推断功能性 MuA 四聚体必须对观察到的四个交叉中的三个做出贡献,从而将增强子限制在复合物中。我们讨论了 MuA 和 DNA 超螺旋对在三叉路口构建的 5 节点 Mu 突触的贡献。