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An Lrp-like Transcriptional Regulator from the ArchaeonPyrococcus furiosus Is Negatively Autoregulated
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 tr...
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Published in: | The Journal of biological chemistry 2000-12, Vol.275 (49), p.38160-38169 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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 that 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 that overlaps the transcriptional start site of its own promoter. The molecular basis
of the transcription inhibition by LrpA is discussed. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M005916200 |