Heidrich Nadja, Brantl Sabine
Friedrich-Schiller-Universität Jena, AG Bakteriengenetik, Philosophenweg 12, D-07743 Jena, Germany.
Microbiology (Reading). 2007 Feb;153(Pt 2):420-427. doi: 10.1099/mic.0.2006/002329-0.
Streptococcal plasmid pIP501 uses antisense RNA-mediated transcriptional attenuation to regulate its replication. Previous in vitro assays suggested that binding intermediates between RNAII (sense RNA) and RNAIII (antisense RNA) are sufficient for inhibition, and a U-turn structure on RNAII loop L1 was found to be crucial for the interaction with RNAIII. Here, sequence and structural requirements for an efficient RNAII-RNAIII interaction were investigated. A detailed probing of RNA secondary structure combined with in vitro single-round transcription assays indicated that complex formation between the two molecules progresses into the lower stems of both loop pairs of the sense and antisense RNAs, but that the complex between RNAII and RNAIII is not a full duplex. Stem-loops L3 and L4 were required to be linked to one other for efficient contact with the complementary loops L2 and L1 of the sense RNA, indicating a simultaneous interaction between these two loop pairs. Thereby, the sequence and length of the spacer connecting L3 and L4 were shown not to be important for inhibition.
链球菌质粒pIP501利用反义RNA介导的转录衰减来调控其复制。先前的体外实验表明,RNAII(正义RNA)和RNAIII(反义RNA)之间的结合中间体足以产生抑制作用,并且发现RNAII环L1上的一个U型结构对于与RNAIII的相互作用至关重要。在此,研究了高效RNAII-RNAIII相互作用的序列和结构要求。对RNA二级结构的详细探测结合体外单轮转录实验表明,两个分子之间的复合物形成过程会延伸到正义和反义RNA的两个环对的下部茎区,但RNAII和RNAIII之间的复合物并非完全双链。茎环L3和L4需要相互连接才能与正义RNA的互补环L2和L1有效接触,这表明这两个环对之间存在同时相互作用。因此,连接L3和L4的间隔区的序列和长度对抑制作用并不重要。