Loot C, Turlan C, Rousseau P, Ton-Hoang B, Chandler M
Laboratoire de Microbiologie et Génétique Moléculaire, CNRS UMR5100, 118 Rte de Narbonne, F-31062 Toulouse Cedex, France.
EMBO J. 2002 Aug 1;21(15):4172-82. doi: 10.1093/emboj/cdf403.
The role played by insertion sequence IS911 proteins, OrfA and OrfAB, in the choice of a target for insertion was studied. IS911 transposition occurs in several steps: synapsis of the two transposon ends (IRR and IRL); formation of a figure-of-eight intermediate where both ends are joined by a single-strand bridge; resolution into a circular form carrying an IRR-IRL junction; and insertion into a DNA target. In vivo, with OrfAB alone, an IS911-based transposon integrated with high probability next to an IS911 end located on the target plasmid. OrfA greatly reduced the proportion of these events. This was confirmed in vitro using a transposon with a preformed IRR-IRL junction to examine the final insertion step. Addition of OrfA resulted in a large increase in insertion frequency and greatly increased the proportion of non-targeted insertions. The intermolecular reaction leading to targeted insertion may resemble the intramolecular reaction involving figure-of-eight molecules, which leads to the formation of circles. OrfA could, therefore, be considered as a molecular switch modulating the site-specific recombination activity of OrfAB and facilitating dispersion of the insertion sequence (IS) to 'non-homologous' target sites.
研究了插入序列IS911蛋白OrfA和OrfAB在选择插入靶点中所起的作用。IS911转座按几个步骤进行:两个转座子末端(IRR和IRL)的联会;形成一个八字形中间体,两端由一条单链桥连接;解析为携带IRR-IRL连接的环状形式;以及插入DNA靶点。在体内,单独使用OrfAB时,基于IS911的转座子极有可能整合到位于目标质粒上的IS911末端旁边。OrfA大大降低了这些事件的比例。这在体外使用具有预先形成的IRR-IRL连接的转座子来检查最终插入步骤时得到了证实。添加OrfA导致插入频率大幅增加,并大大提高了非靶向插入的比例。导致靶向插入的分子间反应可能类似于涉及八字形分子的分子内反应,后者导致环状物的形成。因此,OrfA可被视为一种分子开关,调节OrfAB的位点特异性重组活性,并促进插入序列(IS)向“非同源”靶点的分散。