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 - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q34349964

about

Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli Managing DNA polymerases: coordinating DNA replication, DNA repair, and DNA recombination Historical overview: searching for replication help in all of the rec places RecBCD enzyme and the repair of double-stranded DNA breaks Precise temporal modulation in the response of the SOS DNA repair network in individual bacteria.Rescuing stalled or damaged replication forks Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda Genetic separation of Escherichia coli recA functions for SOS mutagenesis and repressor cleavage.The RecA protein: structure and function.A homolog of Escherichia coli RecA protein in plastids of higher plants Characterization of stress-responsive behavior in Pseudomonas aeruginosa PAO: isolation of Tn3-lacZYA fusions with novel damage-inducible (din) promoters.UmuD mutagenesis protein of Escherichia coli: overproduction, purification, and cleavage by RecA.The bacteriophage P1 HumD protein is a functional homolog of the prokaryotic UmuD'-like proteins and facilitates SOS mutagenesis in Escherichia coli Two distinct modes of RecA action are required for DNA polymerase V-catalyzed translesion synthesis.Nucleotide excision repair or polymerase V-mediated lesion bypass can act to restore UV-arrested replication forks in Escherichia coli.UmuC mutagenesis protein of Escherichia coli: purification and interaction with UmuD and UmuD'.Interactions between epsilon, the proofreading subunit of DNA polymerase III, and proteins involved in the SOS response of Escherichia coli.Mutagenesis and more: umuDC and the Escherichia coli SOS response.A model for a umuDC-dependent prokaryotic DNA damage checkpoint.A phenotype for enigmatic DNA polymerase II: a pivotal role for pol II in replication restart in UV-irradiated Escherichia coli The genetic requirements for UmuDC-mediated cold sensitivity are distinct from those for SOS mutagenesis Loop II of DNA polymerase beta is important for polymerization activity and fidelity.Intermolecular cleavage by UmuD-like mutagenesis proteins Isolation and characterization of novel plasmid-encoded umuC mutants Overproduction of DnaE protein (alpha subunit of DNA polymerase III) restores viability in a conditionally inviable Escherichia coli strain deficient in DNA polymerase I A rapid method for cloning mutagenic DNA repair genes: isolation of umu-complementing genes from multidrug resistance plasmids R391, R446b, and R471a Levels of epsilon, an essential replication subunit of Escherichia coli DNA polymerase III, are controlled by heat shock proteins.Mutagenic DNA repair in enterobacteria.Requirement of RecBC enzyme and an elevated level of activated RecA for induced stable DNA replication in Escherichia coli RecA protein of Escherichia coli has a third essential role in SOS mutator activity.Presence of the dnaQ-rnh divergent transcriptional unit on a multicopy plasmid inhibits induced mutagenesis in Escherichia coli.DNA repair and genome maintenance in Bacillus subtilis.An in vivo complex with DNA photolyase blocks UV mutagenesis targeted at a thymine-cytosine dimer in Escherichia coli Targeting of the UmuD, UmuD', and MucA' mutagenesis proteins to DNA by RecA protein Inhibition of chloroplast DNA recombination and repair by dominant negative mutants of Escherichia coli RecA.Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription SOS induction by stabilized topoisomerase IA cleavage complex occurs via the RecBCD pathway.Activity of the purified mutagenesis proteins UmuC, UmuD', and RecA in replicative bypass of an abasic DNA lesion by DNA polymerase III.Cellular roles of DNA polymerase beta.Discontinuous leading-strand synthesis: a stop-start story.

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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

http://www.wikidata.org/entity/Q34349964

description

1987 nî lūn-bûn

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1987 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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1987 թվականի հոտեմբերին հրատարակված գիտական հոդված

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1987年の論文

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1987年論文

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1987年論文

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1987年論文

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1987年論文

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1987年論文

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1987年论文

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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Proceedings of the National Academy of Sciences of the United States of America

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Recovery from ultraviolet ligh ...... A+ strains of Escherichia coli

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E M Witkin

http://www.w3.org/2001/XMLSchema#string

J B Sweasy

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J O McCall

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V Roegner-Maniscalco

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P2860

Acetylornithinase of Escherichia coli: partial purification and some properties

The origin of replication, oriC, and the dnaA protein are dispensable in stable DNA replication (sdrA) mutants of Escherichia coli K-12.

Amplified RNase H activity in Escherichia coli B/r increases sensitivity to ultraviolet radiation.

Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli.

Capacity of RecA protein to bind preferentially to UV lesions and inhibit the editing subunit (epsilon) of DNA polymerase III: a possible mechanism for SOS-induced targeted mutagenesis.

Constitutive expression of the SOS response in recA718 mutants of Escherichia coli requires amplification of RecA718 protein

RNase H is not involved in the induction of stable DNA replication in Escherichia coli

RNase H-defective mutants of Escherichia coli.

Suppression of tif-mediated induction of SOS functions in Escherichia coli by an altered dnaB protein

Cold sensitivity induced by overproduction of UmuDC in Escherichia coli.

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3309946

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Escherichia coli

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299173

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