Hasselmayer Oliver, Nitsche Claudia, Braun Veit, von Eichel-Streiber Christoph
Verfügungsgebäude für Forschung und Entwicklung, Institut für Medizinische Mikrobiologie und Hygiene, Johannes Gutenberg-Universität, Mainz 55101, Germany.
Anaerobe. 2004 Apr;10(2):85-92. doi: 10.1016/j.anaerobe.2003.12.003.
The IStron CdISt1 was first discovered as an insertion into the tcdA gene of the clinical isolate C34. It combines structural and functional properties of a group I intron at its 5'-end with those of an insertion element at its 3'-end. Up to date four different types could be found, mainly differing in their IS-element portions. Contrasting classical group I introns, CdISt1 is always integrated in ORFs encoding bacterial protein. In case CdISt1 had only the IS-element function such insertion would inactivate the protein encoded by the host gene. It is only due to the self-splicing activity of the group I intron parts that CdISt1 integration does not abolish protein function. Both elements seem to exist in molecular symbiosis and CdISt1 could thus be a prototype of a novel class of genetic elements. Moreover, integration of the CdISt1 into the genome could be advantageous for the bacterium, a motor function for evolution of bacterial proteins is discussed. In clinical practice CdISt1 might well serve as a tool for epidemiological studies of C. difficile infections.
IStron CdISt1最初是在临床分离株C34的tcdA基因中作为插入序列被发现的。它在5'端具有I类内含子的结构和功能特性,在3'端具有插入元件的结构和功能特性。到目前为止,已发现四种不同类型,主要区别在于其IS元件部分。与经典的I类内含子不同,CdISt1总是整合在编码细菌蛋白的开放阅读框中。如果CdISt1仅具有IS元件功能,这种插入会使宿主基因编码的蛋白失活。只是由于I类内含子部分的自我剪接活性,CdISt1的整合才不会消除蛋白功能。这两种元件似乎以分子共生的形式存在,因此CdISt1可能是一类新型遗传元件的原型。此外,CdISt1整合到基因组中可能对细菌有利,文中讨论了其在细菌蛋白进化中的驱动作用。在临床实践中,CdISt1很可能作为艰难梭菌感染流行病学研究的工具。