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An Lrp-like transcriptional regulator from the archaeon Pyrococcus furiosus is negatively autoregulated

Authors :
J.H.G. Lebbink
Isabell Dahlke
Torsten Lammers
John van der Oost
J.E. Tuininga
Arie B. Brinkman
Michael Thomm
Willem M. de Vos
Valerie Dumay
Edwin de Heus
Radiotherapy
Source :
Journal of Biological Chemistry, 275(49), 38160-38169. American Society for Biochemistry and Molecular Biology Inc.
Publication Year :
2000
Publisher :
American Society for Biochemistry and Molecular Biology Inc., 2000.

Abstract

The archaeal transcriptional initiation machinery closely resembles core elements of the eukaryal polymerase II system. However, apart from the established basal archaeal transcription system, little is known about the modulation of gene expression in archaea. At present, no obvious eukaryal-like transcriptional regulators have been identified in archaea. Instead, we have previously isolated an archaeal gene, the Pyrococcus furiosus lrpA, that potentially encodes a bacterial-like transcriptional regulator. In the present study, we have for the first time addressed the actual involvement of an archaeal Lrp homologue in transcription modulation. For that purpose, we have produced LrpA in Escherichia coli. In a cell-free P. furiosus transcription system we used wild-type and mutated lrpA promoter fragments to demonstrate thai the purified LrpA negatively regulates its own transcription. In addition, gel retardation analyses revealed a single protein-DNA complex, in which LrpA appeared to be present in (at least) a tetrameric conformation. The location of the LrpA binding site was further identified by DNaseI and hydroxyl radical footprinting, indicating that LrpA binds to a 46-base pair sequence thai overlaps the transcriptional start site of its own promoter. The molecular basis of the transcription inhibition by LrpA is discussed.

Details

Language :
English
ISSN :
1083351X and 00219258
Volume :
275
Issue :
49
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi.dedup.....a64f52c4dd259d0dafe8a85a25ec71bb