PMID:7556074: Difference between revisions

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<span style = 'font-size: large'> '''Landini, P and Volkert, MR'''  (1995) RNA polymerase alpha subunit binding site in positively controlled promoters: a new model for RNA polymerase-promoter interaction and transcriptional activation in the Escherichia coli ada and aidB genes.''EMBO J.'' '''14''':4329-35</span>
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'''Landini, P and Volkert, MR'''  (1995) RNA polymerase alpha subunit binding site in positively controlled promoters: a new model for RNA polymerase-promoter interaction and transcriptional activation in the Escherichia coli ada and aidB genes. ''EMBO J.'' '''14''':4329-35
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!align=left  |Abstract
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The ada and aidB genes are part of the adaptive response to DNA methylation damage in Escherichia coli. Transcription of the ada and the aidB genes is triggered by binding of the methylated Ada protein (meAda) to a specific sequence located 40-60 base pairs upstream of the transcriptional start, which is internal to an A/T-rich region. In this report we demonstrate that the Ada binding site is also a binding site for RNA polymerase. RNA polymerase is able to bind the -40 to -60 region of the ada and the aidB promoters in the absence of meAda, and its binding is mediated by the alpha subunit. This region resembles the UP element of the rrnB P1 promoter in location, sequence and mechanism of interaction with RNA polymerase. We discuss the function of UP-like elements in positively controlled promoters and provide evidence that Ada does not act by enhancing RNA polymerase binding affinity to the promoter region. Instead, Ada stimulates transcription by modifying the nature of the RNA polymerase-promoter interaction, allowing RNA polymerase to recognize the core promoter -35 and -10 elements in addition to the UP-like element.
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=7556074 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC394517 PMC394517]


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|{{TableHeadingColor}} |'''Abstract''' || The ada and aidB genes are part of the adaptive response to DNA methylation damage in Escherichia coli. Transcription of the ada and the aidB genes is triggered by binding of the methylated Ada protein (meAda) to a specific sequence located 40-60 base pairs upstream of the transcriptional start, which is internal to an A/T-rich region. In this report we demonstrate that the Ada binding site is also a binding site for RNA polymerase. RNA polymerase is able to bind the -40 to -60 region of the ada and the aidB promoters in the absence of meAda, and its binding is mediated by the alpha subunit. This region resembles the UP element of the rrnB P1 promoter in location, sequence and mechanism of interaction with RNA polymerase. We discuss the function of UP-like elements in positively controlled promoters and provide evidence that Ada does not act by enhancing RNA polymerase binding affinity to the promoter region. Instead, Ada stimulates transcription by modifying the nature of the RNA polymerase-promoter interaction, allowing RNA polymerase to recognize the core promoter -35 and -10 elements in addition to the UP-like element.
!align=left  |Keywords
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Bacterial Proteins/biosynthesis; Bacterial Proteins/genetics; Base Sequence; Binding Sites; DNA, Bacterial/isolation & purification; DNA, Bacterial/metabolism; Deoxyribonuclease I; Escherichia coli/genetics; Escherichia coli/metabolism; Escherichia coli Proteins; Genes, Bacterial; Macromolecular Substances; Molecular Sequence Data; O(6)-Methylguanine-DNA Methyltransferase; Promoter Regions, Genetic; RNA Polymerase I/isolation & purification; RNA Polymerase I/metabolism; Restriction Mapping; Transcription Factors; Transcriptional Activation
|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=7556074 PubMed]
 
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Latest revision as of 04:50, 15 September 2013

Citation

Landini, P and Volkert, MR (1995) RNA polymerase alpha subunit binding site in positively controlled promoters: a new model for RNA polymerase-promoter interaction and transcriptional activation in the Escherichia coli ada and aidB genes. EMBO J. 14:4329-35

Abstract

The ada and aidB genes are part of the adaptive response to DNA methylation damage in Escherichia coli. Transcription of the ada and the aidB genes is triggered by binding of the methylated Ada protein (meAda) to a specific sequence located 40-60 base pairs upstream of the transcriptional start, which is internal to an A/T-rich region. In this report we demonstrate that the Ada binding site is also a binding site for RNA polymerase. RNA polymerase is able to bind the -40 to -60 region of the ada and the aidB promoters in the absence of meAda, and its binding is mediated by the alpha subunit. This region resembles the UP element of the rrnB P1 promoter in location, sequence and mechanism of interaction with RNA polymerase. We discuss the function of UP-like elements in positively controlled promoters and provide evidence that Ada does not act by enhancing RNA polymerase binding affinity to the promoter region. Instead, Ada stimulates transcription by modifying the nature of the RNA polymerase-promoter interaction, allowing RNA polymerase to recognize the core promoter -35 and -10 elements in addition to the UP-like element.

Links

PubMed PMC394517

Keywords

Bacterial Proteins/biosynthesis; Bacterial Proteins/genetics; Base Sequence; Binding Sites; DNA, Bacterial/isolation & purification; DNA, Bacterial/metabolism; Deoxyribonuclease I; Escherichia coli/genetics; Escherichia coli/metabolism; Escherichia coli Proteins; Genes, Bacterial; Macromolecular Substances; Molecular Sequence Data; O(6)-Methylguanine-DNA Methyltransferase; Promoter Regions, Genetic; RNA Polymerase I/isolation & purification; RNA Polymerase I/metabolism; Restriction Mapping; Transcription Factors; Transcriptional Activation

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