Chihara Kotaro, Bischler Thorsten, Barquist Lars, Monzon Vivian A, Noda Naohiro, Vogel Jörg, Tsuneda Satoshi
Department of Life Science and Medical Bioscience, Waseda University, Tokyo, Japan.
Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology, Ibaraki, Japan.
mSystems. 2019 Dec 3;4(6):e00590-19. doi: 10.1128/mSystems.00590-19.
Bacterial small noncoding RNAs (sRNAs) play posttranscriptional regulatory roles in cellular responses to changing environmental cues and in adaptation to harsh conditions. Generally, the RNA-binding protein Hfq helps sRNAs associate with target mRNAs to modulate their translation and to modify global RNA pools depending on physiological state. Here, a combination of UV cross-linking immunoprecipitation followed by high-throughput sequencing (CLIP-seq) and total RNA-seq showed that Hfq interacts with different regions of the transcriptome under planktonic versus biofilm conditions. In the present approach, Hfq preferentially interacted with repeats of the AAN triplet motif at mRNA 5' untranslated regions (UTRs) and sRNAs and U-rich sequences at rho-independent terminators. Further transcriptome analysis suggested that the association of sRNAs with Hfq is primarily a function of their expression levels, strongly supporting the notion that the pool of Hfq-associated RNAs is equilibrated by RNA concentration-driven cycling on and off Hfq. Overall, our combinatorial CLIP-seq and total RNA-seq approach highlights conditional sRNA associations with Hfq as a novel aspect of posttranscriptional regulation in The Gram-negative bacterium is ubiquitously distributed in diverse environments and can cause severe biofilm-related infections in at-risk individuals. Although the presence of a large number of putative sRNAs and widely conserved RNA chaperones in this bacterium implies the importance of posttranscriptional regulatory networks for environmental fluctuations, limited information is available regarding the global role of RNA chaperones such as Hfq in the transcriptome, especially under different environmental conditions. Here, we characterize Hfq-dependent differences in gene expression and biological processes in two physiological states: the planktonic and biofilm forms. A combinatorial comparative CLIP-seq and total RNA-seq approach uncovered condition-dependent association of RNAs with Hfq and expands the potential direct regulatory targets of Hfq in the transcriptome.
细菌小非编码RNA(sRNA)在细胞对不断变化的环境线索的反应以及对恶劣条件的适应中发挥转录后调控作用。一般来说,RNA结合蛋白Hfq帮助sRNA与靶mRNA结合,以调节它们的翻译,并根据生理状态改变全局RNA库。在这里,紫外线交联免疫沉淀后高通量测序(CLIP-seq)与总RNA测序相结合的方法表明,在浮游与生物膜条件下,Hfq与转录组的不同区域相互作用。在本方法中,Hfq优先与mRNA 5'非翻译区(UTR)的AAN三联体基序重复序列以及sRNA和不依赖rho的终止子处富含U的序列相互作用。进一步的转录组分析表明,sRNA与Hfq的结合主要是其表达水平的函数,有力地支持了这样一种观点,即与Hfq相关的RNA库通过RNA浓度驱动的与Hfq结合和解离的循环达到平衡。总体而言,我们的CLIP-seq与总RNA测序相结合的方法突出了sRNA与Hfq的条件依赖性结合,这是革兰氏阴性菌转录后调控的一个新方面。革兰氏阴性菌广泛分布于各种环境中,可在高危个体中引起严重的生物膜相关感染。尽管该细菌中存在大量假定的sRNA和广泛保守的RNA伴侣,这意味着转录后调控网络对环境波动很重要,但关于RNA伴侣如Hfq在转录组中的全局作用,尤其是在不同环境条件下的信息有限。在这里,我们描述了Hfq在浮游和生物膜两种生理状态下基因表达和生物学过程中的依赖性差异。CLIP-seq与总RNA测序相结合的比较方法揭示了RNA与Hfq的条件依赖性结合,并扩展了Hfq在转录组中的潜在直接调控靶点。