Source:http://linkedlifedata.com/resource/pubmed/id/16115199
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2005-8-23
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pubmed:abstractText |
Cra (or FruR), a global transcription factor with both repression and activation activities, controls a large number of the genes for glycolysis and gluconeogenesis. To get insights into the entire network of transcription regulation of the E. coli genome by Cra, we isolated a set of Cra-binding sequences using an improved method of genomic SELEX. From the DNA sequences of 97 independently isolated DNA fragments by SELEX, the Cra-binding sequences were identified in a total of ten regions on the E. coli genome, including promoters of six known genes and four hitherto-unidentified genes. All six known promoters are repressed by Cra, but none of the activation-type promoters were cloned after two cyles of SELEX, because the Cra-binding affinity to the repression-type promoters is higher than the activation-type promoters, as determined by the quantitative gel shift assay. Of a total of four newly identified Cra-binding sequences, two are associated with promoter regions of the gapA (glyceraldehyde 3-phosphate dehydrogenase) and eno (enolase) genes, both involved in sugar metabolism. The regulation of newly identified genes by Cra was confirmed by the in vivo promoter strength assay using a newly developed TFP (two-fluorescent protein) vector for promoter assay or by in vitro transcription assay in the presence of Cra protein.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Escherichia coli Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/FruR protein, Bacteria,
http://linkedlifedata.com/resource/pubmed/chemical/Glyceraldehyde-3-Phosphate...,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphopyruvate Hydratase,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1356-9597
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
907-18
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16115199-Bacterial Proteins,
pubmed-meshheading:16115199-Base Sequence,
pubmed-meshheading:16115199-Consensus Sequence,
pubmed-meshheading:16115199-Dose-Response Relationship, Drug,
pubmed-meshheading:16115199-Electrophoretic Mobility Shift Assay,
pubmed-meshheading:16115199-Escherichia coli Proteins,
pubmed-meshheading:16115199-Gene Expression Regulation, Bacterial,
pubmed-meshheading:16115199-Genome, Bacterial,
pubmed-meshheading:16115199-Genomic Library,
pubmed-meshheading:16115199-Genomics,
pubmed-meshheading:16115199-Glyceraldehyde-3-Phosphate Dehydrogenases,
pubmed-meshheading:16115199-Molecular Sequence Data,
pubmed-meshheading:16115199-Open Reading Frames,
pubmed-meshheading:16115199-Phosphopyruvate Hydratase,
pubmed-meshheading:16115199-Promoter Regions, Genetic,
pubmed-meshheading:16115199-Repressor Proteins,
pubmed-meshheading:16115199-Transcription, Genetic
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pubmed:year |
2005
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pubmed:articleTitle |
Systematic search for the Cra-binding promoters using genomic SELEX system.
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pubmed:affiliation |
Nippon Institute for Biological Science, Division of Molecular Biology, Ome, Tokyo 198-0024, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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