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!align=left |Citation | |||
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'''Foti, JJ and Walker, GC''' (2011) Efficient extension of slipped DNA intermediates by DinB is required to escape primer template realignment by DnaQ. ''J. Bacteriol.'' '''193''':2637-41 | |||
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!align=left |Abstract | |||
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We show that Escherichia coli DinB polymerase, which creates single-base deletions, prefers to extend slipped DNA substrates with the skipped base at the -4 position. A DinB(Y79L) variant, which extends these substrates less efficiently in vitro, allows the proofreading function of polymerase III to reverse their formation in vivo. | |||
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!align=left |Links | |||
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=21421753 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133156 PMC3133156] | |||
Online version:[http://dx.doi.org/10.1128/JB.00005-11 10.1128/JB.00005-11] | |||
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!align=left |Keywords | |||
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Amino Acid Substitution/genetics; DNA Polymerase III/metabolism; DNA Replication; DNA, Bacterial/biosynthesis; Escherichia coli/enzymology; Escherichia coli/physiology; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Models, Biological; Mutant Proteins/genetics; Mutant Proteins/metabolism; Mutation, Missense; Sequence Deletion | |||
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==Significance {{HelpIcon|Help:Literature}} == | |||
{{LitSignificance}} | |||
== Useful Materials and Methods {{HelpIcon|Help:Literature}}== | |||
{{LitMaterials}} | |||
==Annotations {{HelpIcon|Help:Literature}}== | |||
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==EcoliWiki Links {{HelpIcon|Help:Literature}} == | |||
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==See also== | |||
==References== | |||
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Latest revision as of 04:38, 15 September 2013
| Citation |
Foti, JJ and Walker, GC (2011) Efficient extension of slipped DNA intermediates by DinB is required to escape primer template realignment by DnaQ. J. Bacteriol. 193:2637-41 |
|---|---|
| Abstract |
We show that Escherichia coli DinB polymerase, which creates single-base deletions, prefers to extend slipped DNA substrates with the skipped base at the -4 position. A DinB(Y79L) variant, which extends these substrates less efficiently in vitro, allows the proofreading function of polymerase III to reverse their formation in vivo. |
| Links |
PubMed PMC3133156 Online version:10.1128/JB.00005-11 |
| Keywords |
Amino Acid Substitution/genetics; DNA Polymerase III/metabolism; DNA Replication; DNA, Bacterial/biosynthesis; Escherichia coli/enzymology; Escherichia coli/physiology; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Models, Biological; Mutant Proteins/genetics; Mutant Proteins/metabolism; Mutation, Missense; Sequence Deletion |
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