Morita Teppei, Nishino Ryo, Aiba Hiroji
Faculty of Pharmaceutical Sciences, Suzuka University of Medical Sciences, Suzuka, Mie, 513-8670, Japan.
RNA. 2017 Sep;23(9):1419-1431. doi: 10.1261/rna.060756.117. Epub 2017 Jun 12.
Rho-independent transcription terminators of the genes encoding bacterial Hfq-binding sRNAs possess a set of seven or more T residues at the 3' end, as noted in previous studies. Here, we have studied the role of the terminator hairpin in the biogenesis of sRNAs focusing on SgrS and RyhB in We constructed variant sRNA genes in which the GC-rich inverted repeat sequences are extended to stabilize the terminator hairpins. We demonstrate that the extension of the hairpin stem leads to generation of heterogeneous transcripts in which the poly(U) tail is shortened. The transcripts with shortened poly(U) tails no longer bind to Hfq and lose the ability to repress the target mRNAs. The shortened transcripts are generated in an in vitro transcription system with purified RNA polymerase, indicating that the generation of shortened transcripts is caused by premature transcription termination. We conclude that the terminator structure of sRNA genes is optimized to generate functional sRNAs. Thus, the Rho-independent terminators of sRNA genes possess two common features: a long T residue stretch that is a prerequisite for generation of functional sRNAs and a moderate strength of hairpin structure that ensures the termination at the seventh or longer position within the consecutive T stretch. The modulation of the termination position at the Rho-independent terminators is critical for biosynthesis of functional sRNAs.
如先前研究所指出的,编码细菌Hfq结合小RNA的基因的不依赖Rho的转录终止子在3'端具有一组七个或更多的T残基。在这里,我们以SgrS和RyhB为重点,研究了终止子发夹在小RNA生物合成中的作用。我们构建了变体小RNA基因,其中富含GC的反向重复序列被延长以稳定终止子发夹。我们证明发夹茎的延长导致产生异质转录本,其中聚(U)尾巴缩短。聚(U)尾巴缩短的转录本不再与Hfq结合,并失去抑制靶标mRNA的能力。缩短的转录本是在含有纯化RNA聚合酶的体外转录系统中产生的,这表明缩短转录本的产生是由过早的转录终止引起的。我们得出结论,小RNA基因的终止子结构经过优化以产生功能性小RNA。因此,小RNA基因的不依赖Rho的终止子具有两个共同特征:一个长的T残基延伸,这是产生功能性小RNA的先决条件;以及适度强度的发夹结构,可确保在连续T延伸内的第七个或更长位置处终止。不依赖Rho的终止子处终止位置的调节对于功能性小RNA的生物合成至关重要。