Rochat Tatiana, Delumeau Olivier, Figueroa-Bossi Nara, Noirot Philippe, Bossi Lionello, Dervyn Etienne, Bouloc Philippe
Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, F-91405, Orsay, France; INRA, UR892, Virologie et Immunologie Moléculaires, F-78352, Jouy-en-Josas, France.
INRA, UMR1319 Micalis, F-78350, Jouy-en-Josas, France; AgroParisTech, UMR Micalis, F-78350, Jouy-en-Josas, France.
PLoS One. 2015 Apr 27;10(4):e0124977. doi: 10.1371/journal.pone.0124977. eCollection 2015.
RNA-binding protein Hfq is a key component of the adaptive responses of many proteobacterial species including Escherichia coli, Salmonella enterica and Vibrio cholera. In these organisms, the importance of Hfq largely stems from its participation to regulatory mechanisms involving small non-coding RNAs. In contrast, the function of Hfq in Gram-positive bacteria has remained elusive and somewhat controversial. In the present study, we have further addressed this point by comparing growth phenotypes and transcription profiles between wild-type and an hfq deletion mutant of the model Gram-positive bacterium, Bacillus subtilis. The absence of Hfq had no significant consequences on growth rates under nearly two thousand metabolic conditions and chemical treatments. The only phenotypic difference was a survival defect of B. subtilis hfq mutant in rich medium in stationary phase. Transcriptomic analysis correlated this phenotype with a change in the levels of nearly one hundred transcripts. Albeit a significant fraction of these RNAs (36%) encoded sporulation-related functions, analyses in a strain unable to sporulate ruled out sporulation per se as the basis of the hfq mutant's stationary phase fitness defect. When expressed in Salmonella, B. subtilis hfq complemented the sharp loss of viability of a degP hfq double mutant, attenuating the chronic σE-activated phenotype of this strain. However, B. subtilis hfq did not complement other regulatory deficiencies resulting from loss of Hfq-dependent small RNA activity in Salmonella indicating a limited functional overlap between Salmonella and B. subtilis Hfqs. Overall, this study confirmed that, despite structural similarities with other Hfq proteins, B. subtilis Hfq does not play a central role in post-transcriptional regulation but might have a more specialized function connected with stationary phase physiology. This would account for the high degree of conservation of Hfq proteins in all 17 B. subtilis strains whose genomes have been sequenced.
RNA结合蛋白Hfq是许多变形菌适应性反应的关键组成部分,包括大肠杆菌、肠炎沙门氏菌和霍乱弧菌。在这些生物体中,Hfq的重要性很大程度上源于其参与涉及小非编码RNA的调控机制。相比之下,Hfq在革兰氏阳性菌中的功能仍然难以捉摸且存在一定争议。在本研究中,我们通过比较模式革兰氏阳性菌枯草芽孢杆菌的野生型和hfq缺失突变体之间的生长表型和转录谱,进一步探讨了这一问题。在近两千种代谢条件和化学处理下,Hfq的缺失对生长速率没有显著影响。唯一的表型差异是枯草芽孢杆菌hfq突变体在稳定期丰富培养基中的生存缺陷。转录组分析将这种表型与近一百个转录本水平的变化相关联。尽管这些RNA中有很大一部分(36%)编码与芽孢形成相关的功能,但在一个无法形成芽孢的菌株中的分析排除了芽孢形成本身是hfq突变体稳定期适应性缺陷的基础。当在沙门氏菌中表达时,枯草芽孢杆菌hfq补充了degP hfq双突变体活力的急剧丧失,减轻了该菌株慢性σE激活的表型。然而,枯草芽孢杆菌hfq并没有补充沙门氏菌中由于Hfq依赖性小RNA活性丧失而导致的其他调控缺陷,这表明沙门氏菌和枯草芽孢杆菌的Hfqs之间功能重叠有限。总体而言,本研究证实,尽管枯草芽孢杆菌Hfq与其他Hfq蛋白在结构上有相似之处,但它在转录后调控中并不起核心作用,可能具有与稳定期生理学相关的更特殊功能。这可以解释在已测序基因组的所有17株枯草芽孢杆菌中Hfq蛋白的高度保守性。