Coping with replication 'train wrecks' in Escherichia coli using Pol V, Pol II and RecA proteins (Q33885426)

29 July 2017

title

Coping with replication 'train wrecks' in Escherichia coli using Pol V, Pol II and RecA proteins (English)

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29 July 2017

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Goodman MF

1

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29 July 2017

publication date

1 April 2000

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29 July 2017

number of pages

7

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Trends in Biochemical Sciences

inferred from page(s)

published in

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29 July 2017

volume

25

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29 July 2017

issue

4

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29 July 2017

page(s)

189-195

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publication type of scholarly work

29 July 2017

review article

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Inducible DNA repair systems

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The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication

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Mechanism of transient inhibition of DNA synthesis in ultraviolet-irradiated E. coli: inhibition is independent of recA whilst recovery requires RecA protein itself and an additional, inducible SOS function

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Recovery from ultraviolet light-induced inhibition of DNA synthesis requires umuDC gene products in recA718 mutant strains but not in recA+ strains of Escherichia coli

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Frequency and spectrum of mutations produced by a single cis-syn thymine-thymine cyclobutane dimer in a single-stranded vector

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The thymine-thymine pyrimidine-pyrimidone(6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli

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RecA protein of Escherichia coli has a third essential role in SOS mutator activity

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UmuC mutagenesis protein of Escherichia coli: purification and interaction with UmuD and UmuD'.

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Activity of the purified mutagenesis proteins UmuC, UmuD', and RecA in replicative bypass of an abasic DNA lesion by DNA polymerase III

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Construction of a umuDC operon substitution mutation in Escherichia coli

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The Mutagenesis Proteins UmuD′ and UmuC Prevent Lethal Frameshifts While Increasing Base Substitution Mutations

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DNA polymerase III of Escherichia coli is required for UV and ethyl methanesulfonate mutagenesis

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Interaction of recA protein with single-stranded DNA. Quantitative aspects of binding affinity modulation by nucleotide cofactors

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Levels of chromosomally encoded Umu proteins and requirements for in vivo UmuD cleavage

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The 'A rule' of mutagen specificity: a consequence of DNA polymerase bypass of non-instructional lesions?

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Identifiers

DOI

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29 July 2017

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