Balancing metal uptake is essential for maintaining proper intracellular metal concentration. Here we report the transcriptional control exerted by the two metal-responsive regulators of Helicobacter pylori, Fur (iron-dependent ferric uptake regulator) and NikR (nickel-responsive regulator), on the three copies of the fecA genes present in this species. By following the patterns of transcription throughout growth and in response to nickel, iron and a metal chelator, we found that the expression of the three fecA genes is temporally regulated, responds differently to metals 9 and is selectively controlled by either one of the two regulators. fecA1 is expressed at a constant level throughout growth and its expression is iron-sensitive; the expression of fecA2 is mainly off, with minor expression coming up in late exponential phase. By contrast, the expression of fecA3 is maximal in early exponential phase, gradually decreases with time and is repressed by nickel. The direct role of Fur and NikR was studied both in vitro, by mapping the binding sites of each regulator on the promoter regions via DNaseI footprinting analysis, and in vivo by primer extension analyses of the fecA transcripts in fur and nikR deletion strains. The resulting picture suggests dedicated feedback regulatory circuits, where each FecA homologue is likely to be required for the selective import of metals and its expression is specifically controlled at the transcriptional level by the metal responsive regulator.
A. Danielli, S. Romagnoli, D. Roncarati, L. Costantino, I. Delany, V. Scarlato (2009). Growth phase and metal-dependent transcriptional regulation of the fecA genes in Helicobacter pylori. JOURNAL OF BACTERIOLOGY, 191 (11), 3717-3725.
Growth phase and metal-dependent transcriptional regulation of the fecA genes in Helicobacter pylori
DANIELLI, ALBERTO;ROMAGNOLI, SIMONA;RONCARATI, DAVIDE;SCARLATO, VINCENZO
2009
Abstract
Balancing metal uptake is essential for maintaining proper intracellular metal concentration. Here we report the transcriptional control exerted by the two metal-responsive regulators of Helicobacter pylori, Fur (iron-dependent ferric uptake regulator) and NikR (nickel-responsive regulator), on the three copies of the fecA genes present in this species. By following the patterns of transcription throughout growth and in response to nickel, iron and a metal chelator, we found that the expression of the three fecA genes is temporally regulated, responds differently to metals 9 and is selectively controlled by either one of the two regulators. fecA1 is expressed at a constant level throughout growth and its expression is iron-sensitive; the expression of fecA2 is mainly off, with minor expression coming up in late exponential phase. By contrast, the expression of fecA3 is maximal in early exponential phase, gradually decreases with time and is repressed by nickel. The direct role of Fur and NikR was studied both in vitro, by mapping the binding sites of each regulator on the promoter regions via DNaseI footprinting analysis, and in vivo by primer extension analyses of the fecA transcripts in fur and nikR deletion strains. The resulting picture suggests dedicated feedback regulatory circuits, where each FecA homologue is likely to be required for the selective import of metals and its expression is specifically controlled at the transcriptional level by the metal responsive regulator.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.