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FurA modulates gene expression of alr3808, a DpsA homologue in Nostoc (Anabaena) sp. PCC7120
Authors:Hernández José A  Pellicer Silvia  Huang Lionel  Peleato M Luisa  Fillat María F
Institution:a Department of Biochemistry and Molecular and Cell Biology, University of Zaragoza, Pedro Cerbuna 12, 50009-Zaragoza, Spain
b Biocomputation and Complex Systems Physics Institute (BiFi), University of Zaragoza, Pedro Cerbuna 12, 50009-Zaragoza, Spain
Abstract:The DNA-binding protein from stationary phase (Dps) protein family plays an important role in protecting microorganisms from oxidative and nutritional stresses. In silico analysis of the promoter region of alr3808, a dpsA homologue from the cyanobacterium Nostoc sp. PCC7120 shows putative iron-boxes with high homology with those recognized by FurA (ferric uptake regulator). Evidence for the modulation of dpsA by FurA was obtained using in vitro and in vivo approaches. SELEX linked to PCR was used to identify PdpsA as a FurA target. Concurrently, EMSA assays showed high affinity of FurA for the dpsA promoter region. DpsA expression analysis in an insertional mutant of the alr1690-αfurA message (that exhibited an increased expression of FurA) showed a reduced synthesis of DpsA. These studies suggest that FurA plays a significant role in the regulation of the DpsA.
Keywords:Dps  DNA-binding protein from stationary phase  Fur  ferric uptake regulator  SELEX  systematic evolution of ligands by exponential enrichment  EMSA  electrophoretic mobility shift assays
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