Zhan Yuhua, Yan Yongliang, Deng Zhiping, Chen Ming, Lu Wei, Lu Chao, Shang Liguo, Yang Zhimin, Zhang Wei, Wang Wei, Li Yun, Ke Qi, Lu Jiasi, Xu Yuquan, Zhang Liwen, Xie Zhihong, Cheng Qi, Elmerich Claudine, Lin Min
National Key Facility for Crop Gene Resources and Genetic Improvement, Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China;
Key Laboratory of Coastal Biology and Bioresource Utilization, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, China;
Proc Natl Acad Sci U S A. 2016 Jul 26;113(30):E4348-56. doi: 10.1073/pnas.1604514113. Epub 2016 Jul 12.
Unlike most Pseudomonas, the root-associated bacterium Pseudomonas stutzeri A1501 fixes nitrogen after the horizontal acquisition of a nitrogen-fixing (nif) island. A genome-wide search for small noncoding RNAs (ncRNAs) in P. stutzeri A1501 identified the novel P. stutzeri-specific ncRNA NfiS in the core genome, whose synthesis was significantly induced under nitrogen fixation or sorbitol stress conditions. The expression of NfiS was RNA chaperone Hfq-dependent and activated by the sigma factor RpoN/global nitrogen activator NtrC/nif-specific activator NifA regulatory cascade. The nfiS-deficient mutant displayed reduced nitrogenase activity, as well as increased sensitivity to multiple stresses, such as osmotic and oxidative stresses. Secondary structure prediction and complementation studies confirmed that a stem-loop structure was essential for NfiS to regulate the nitrogenase gene nifK mRNA synthesis and thus nitrogenase activity. Microscale thermophoresis and physiological analysis showed that NfiS directly pairs with nifK mRNA and ultimately enhances nitrogenase activity by increasing the translation efficiency and the half-life of nifK mRNA. Our data also suggest structural and functional divergence of NfiS evolution in diazotrophic and nondiazotrophic backgrounds. It is proposed that NfiS was recruited by nifK mRNA as a novel regulator to integrate the horizontally acquired nif island into host global networks.
与大多数假单胞菌不同,根部相关细菌施氏假单胞菌A1501在水平获得固氮(nif)岛后能够固氮。对施氏假单胞菌A1501进行全基因组范围内的小非编码RNA(ncRNA)搜索,在核心基因组中鉴定出了新型的施氏假单胞菌特异性ncRNA NfiS,其合成在固氮或山梨醇胁迫条件下显著诱导。NfiS的表达依赖于RNA伴侣蛋白Hfq,并由σ因子RpoN/全局氮激活因子NtrC/nif特异性激活因子NifA调控级联激活。nfiS缺陷型突变体表现出固氮酶活性降低,以及对多种胁迫(如渗透胁迫和氧化胁迫)的敏感性增加。二级结构预测和互补研究证实,茎环结构对于NfiS调节固氮酶基因nifK mRNA的合成从而调节固氮酶活性至关重要。微量热泳动和生理学分析表明,NfiS直接与nifK mRNA配对,并最终通过提高nifK mRNA的翻译效率和半衰期来增强固氮酶活性。我们的数据还表明,NfiS在固氮和非固氮背景下的进化存在结构和功能差异。有人提出,NfiS被nifK mRNA招募为一种新型调节因子,以将水平获得的nif岛整合到宿主全局网络中。