Lee Hyun-Jung, Bang So Hyun, Lee Kyu-Ho, Park Soon-Jung
Department of Parasitology, Yonsei University School of Medicine, 134 Shinchon-dong, Seodaemun-gu, Seoul 152-750, Republic of Korea.
J Bacteriol. 2007 Apr;189(7):2629-36. doi: 10.1128/JB.01791-06. Epub 2007 Jan 19.
In pathogenic bacteria, the ability to acquire iron, which is mainly regulated by the ferric uptake regulator (Fur), is essential to maintain growth as well as its virulence. In Vibrio vulnificus, a human pathogen causing gastroenteritis and septicemia, fur gene expression is positively regulated by Fur when the iron concentration is limited (H.-J. Lee et al., J. Bacteriol. 185:5891-5896, 2003). Footprinting analysis revealed that an upstream region of the fur gene was protected by the Fur protein from DNase I under iron-depleted conditions. The protected region, from -142 to -106 relative to the transcription start site of the fur gene, contains distinct AT-rich repeats. Mutagenesis of this repeated sequence resulted in abolishment of binding by Fur. To confirm the role of this cis-acting element in Fur-mediated control of its own gene in vivo, fur expression was monitored in V. vulnificus strains using a transcriptional fusion containing the mutagenized Fur-binding site (fur(mt)::luxAB). Expression of fur(mt)::luxAB showed that it was not regulated by Fur and was not influenced by iron concentration. Therefore, this study demonstrates that V. vulnificus Fur acts as a positive regulator under iron-limited conditions by direct interaction with the fur upstream region.
在致病细菌中,获取铁的能力对于维持其生长和毒力至关重要,而这一能力主要受铁摄取调节蛋白(Fur)调控。创伤弧菌是一种可引发肠胃炎和败血症的人类病原体,当铁浓度有限时,fur基因的表达受到Fur的正向调控(H.-J. Lee等人,《细菌学杂志》185:5891 - 5896,2003年)。足迹分析表明,在缺铁条件下,fur基因的上游区域受到Fur蛋白的保护,免受DNase I的作用。相对于fur基因转录起始位点,该受保护区域从-142到-106,包含不同的富含AT的重复序列。对该重复序列进行诱变导致Fur无法结合。为了在体内证实这个顺式作用元件在Fur介导的自身基因调控中的作用,利用含有诱变的Fur结合位点(fur(mt)::luxAB)的转录融合,在创伤弧菌菌株中监测fur的表达。fur(mt)::luxAB的表达表明它不受Fur调控,也不受铁浓度影响。因此,本研究证明创伤弧菌Fur在铁限制条件下通过与fur上游区域直接相互作用而作为正向调节因子发挥作用。