Hopp Crystal M, Gardner Jeffrey F, Salyers Abigail A
Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Plasmid. 2015 Sep;81:63-71. doi: 10.1016/j.plasmid.2015.07.002. Epub 2015 Jul 23.
CTnDOT is a 65kbp integrative and conjugative element (ICE) that carries genes encoding both tetracycline and erythromycin resistances. The excision operon of this element encodes Xis2c, Xis2d, and Exc proteins involved in the excision of CTnDOT from host chromosomes. These proteins are also required in the complex transcriptional regulation of the divergently transcribed transfer (tra) and mobilization (mob) operons of CTnDOT. Transcription of the tra operon is positively regulated by Xis2c and Xis2d, whereas, transcription of the mob operon is positively regulated by Xis2d and Exc. Xis2d is the only protein that is involved in the excision reaction, as well as the transcriptional regulation of both the mob and tra operons. This paper helps establish how Xis2d binds the DNA in the mob and tra region. Unlike other excisionase proteins, Xis2d binds a region of dyad symmetry. The binding site is located in the intergenic region between the mob and tra promoters, and once bound Xis2d induces a bend in the DNA. Xis2d binding to this region could be the preliminary step for the activation of both operons. Then the other proteins, like Exc, can interact with Xis2d and form higher order complexes.
CTnDOT是一个65千碱基对的整合性接合元件(ICE),它携带编码四环素和红霉素抗性的基因。该元件的切除操纵子编码参与CTnDOT从宿主染色体上切除的Xis2c、Xis2d和Exc蛋白。这些蛋白在CTnDOT的反向转录转移(tra)和动员(mob)操纵子的复杂转录调控中也是必需的。tra操纵子的转录受Xis2c和Xis2d正向调控,而mob操纵子的转录受Xis2d和Exc正向调控。Xis2d是唯一参与切除反应以及mob和tra操纵子转录调控的蛋白。本文有助于确定Xis2d如何结合mob和tra区域的DNA。与其他切除酶蛋白不同,Xis2d结合一个二元对称区域。结合位点位于mob和tra启动子之间的基因间区域,一旦结合,Xis2d会诱导DNA弯曲。Xis2d与该区域的结合可能是两个操纵子激活的初步步骤。然后其他蛋白,如Exc,可以与Xis2d相互作用并形成更高阶的复合物。