Pannekoek Yvonne, Huis In 't Veld Robert, Schipper Kim, Bovenkerk Sandra, Kramer Gertjan, Speijer Dave, van der Ende Arie
Department of Medical Microbiology Center for Infection and Immunity Amsterdam (CINIMA) Academic Medical Center The Netherlands.
Department of Medical Biochemistry Academic Medical Center Amsterdam The Netherlands.
FEBS Open Bio. 2017 Aug 5;7(9):1302-1315. doi: 10.1002/2211-5463.12266. eCollection 2017 Sep.
NrrF is a small regulatory RNA of the human pathogen . NrrF was previously shown to repress succinate dehydrogenase () under control of the ferric uptake regulator (Fur). Here, we provide evidence that cytochrome , encoded by the polycistronic mRNA , is a NrrF target as well. We demonstrated differential expression of cytochrome comparing wild-type meningococci and meningococci expressing NrrF when sufficient iron is available. Using a -reporter system monitoring translational control and target recognition of sRNA in , we show that interaction between NrrF and the 5' untranslated region of the mRNA results in its repression. The NrrF region essential for repression of was identified by site-directed mutagenesis and is fully conserved among meningococci. Our results provide further insights into the mechanism by which Fur controls essential components of the respiratory chain. Adaptation of cytochrome complex component levels upon iron limitation is post-transcriptionally regulated via the small regulatory RNA NrrF.
NrrF是人类病原体的一种小调节RNA。先前研究表明,NrrF在铁摄取调节因子(Fur)的控制下抑制琥珀酸脱氢酶。在此,我们提供证据表明,由多顺反子mRNA编码的细胞色素也是NrrF的靶标。我们证明,在有足够铁的情况下,比较野生型脑膜炎球菌和表达NrrF的脑膜炎球菌时,细胞色素存在差异表达。使用监测sRNA在体内翻译控制和靶标识别的报告系统,我们表明NrrF与mRNA的5'非翻译区之间的相互作用导致其受到抑制。通过定点诱变确定了抑制所必需的NrrF区域,该区域在脑膜炎球菌中完全保守。我们的结果为Fur控制呼吸链必需成分的机制提供了进一步的见解。铁限制时细胞色素复合物成分水平的适应性变化是通过小调节RNA NrrF进行转录后调控的。