Moreno Renata, Ruiz-Manzano Ana, Yuste Luis, Rojo Fernando
Departamento de Biotecnología Microbiana, Centro Nacional de Biotecnología, CSIC, Campus de la Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
Mol Microbiol. 2007 May;64(3):665-75. doi: 10.1111/j.1365-2958.2007.05685.x.
The Crc protein is a global regulator that controls the hierarchical assimilation of carbon sources in Pseudomonads by inhibiting expression of several catabolic pathways. Crc does not bind DNA and its mechanism of action has remained elusive. Among other genes, Crc inhibits expression of alkS, the transcriptional activator of the Pseudomonas putida OCT plasmid alkane degradation pathway. AlkS activates expression of its own gene. In the presence of saturating AlkS levels, translational fusions of alkS to the lacZ reporter gene were responsive to Crc, but transcriptional fusions were not. In translational fusions, the first 33 nt of alkS mRNA, which includes up to position +3 relative to the translation start site, were sufficient to confer an efficient response to Crc. In vitro, purified Crc could bind specifically to an alkS mRNA fragment spanning positions +1 to +43, comprising the translation initiation region. We have previously shown that Crc has little effect on the stability of alkS mRNA. We conclude that Crc modulates AlkS levels by binding to the translation initiation region of alkS mRNA, thereby inhibiting translation. Because AlkS is an unstable protein present in limiting amounts, reducing its levels leads to decreased expression of all genes in the pathway.
Crc蛋白是一种全局调控因子,它通过抑制几种分解代谢途径的表达来控制假单胞菌中碳源的分级同化。Crc不与DNA结合,其作用机制一直难以捉摸。在其他基因中,Crc抑制alkS的表达,alkS是恶臭假单胞菌OCT质粒烷烃降解途径的转录激活因子。AlkS激活其自身基因的表达。在AlkS水平饱和的情况下,alkS与lacZ报告基因的翻译融合对Crc有反应,但转录融合则没有。在翻译融合中,alkS mRNA的前33个核苷酸,包括相对于翻译起始位点的+3位置,足以赋予对Crc的有效反应。在体外,纯化的Crc可以特异性结合跨越+1至+43位置的alkS mRNA片段,该片段包含翻译起始区域。我们之前已经表明Crc对alkS mRNA的稳定性影响很小。我们得出结论,Crc通过与alkS mRNA的翻译起始区域结合来调节AlkS水平,从而抑制翻译。由于AlkS是一种不稳定的蛋白质,含量有限,降低其水平会导致该途径中所有基因的表达下降。