Centre National de la Recherche Scientifique, LMGM, F-31000 Toulouse, France.
Mob DNA. 2010 Jun 16;1(1):16. doi: 10.1186/1759-8753-1-16.
Tight regulation of transposition activity is essential to limit damage transposons may cause by generating potentially lethal DNA rearrangements. Assembly of a bona fide protein-DNA complex, the transpososome, within which transposition is catalysed, is a crucial checkpoint in this regulation. In the case of IS911, a member of the large IS3 bacterial insertion sequence family, the transpososome (synaptic complex A; SCA) is composed of the right and left inverted repeated DNA sequences (IRR and IRL) bridged by the transposase, OrfAB (the IS911-encoded enzyme that catalyses transposition). To characterise further this important protein-DNA complex in vitro, we used different tagged and/or truncated transposase forms and analysed their interaction with IS911 ends using gel electrophoresis. Our results allow us to propose a model in which SCA is assembled with a dimeric form of the transposase. Furthermore, we present atomic force microscopy results showing that the terminal inverted repeat sequences are probably assembled in a parallel configuration within the SCA. These results represent the first step in the structural description of the IS911 transpososome, and are discussed in comparison with the very few other transpososome examples described in the literature.
转座活性的严格调控对于限制转座子通过产生潜在致死的 DNA 重排而造成的损害至关重要。转座酶(IS911 编码的酶,催化转座)将转座子(真正的蛋白-DNA 复合物,转座体)内的转位催化,这是这种调控的一个关键检查点。在 IS911 的情况下,它是大型 IS3 细菌插入序列家族的成员,转座体(突触复合物 A;SCA)由转座酶 OrfAB 桥接的右和左反向重复 DNA 序列(IRR 和 IRL)组成。为了在体外进一步表征这个重要的蛋白-DNA 复合物,我们使用了不同标记和/或截断的转座酶形式,并使用凝胶电泳分析它们与 IS911 末端的相互作用。我们的结果允许我们提出一个模型,其中 SCA 是与转座酶的二聚体形式组装的。此外,我们展示了原子力显微镜结果,表明末端反向重复序列可能在 SCA 内以平行配置组装。这些结果代表了 IS911 转座体结构描述的第一步,并与文献中描述的极少数其他转座体例子进行了讨论。