RAD51- and MRE11-dependent reassembly of uncoupled CMG helicase complex at collapsed replication forks

Autor: Vincenzo Costanzo, Fabio Puddu, Yoshitami Hashimoto
Přispěvatelé: Y., Hashimoto, F., Puddu, Costanzo, Vincenzo
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Male
genetics/metabolism
Protein Binding
Rad51 Recombinase

Animals
Blotting

Xenopus
Cell Cycle Proteins
Xenopus Proteins
Western
Carrier Protein

genetics/metabolism
Recombinant Protein

Xenopus laevis
chemistry.chemical_compound
0302 clinical medicine
Structural Biology
MRE11 Homologue Protein
Electrophoresis
Agar Gel

0303 health sciences
Single-Stranded
DNA-Binding Protein

biology
metabolism
Comet Assay
DNA Damage
DNA Helicase

genetics/metabolism
DNA Replication
DNA

Chromatin
Recombinant Proteins
Agar Gel
Female
Male
Multiprotein Complexe

Cell biology
DNA-Binding Proteins
Female
Comet Assay
genetics/metabolism
Electrophoresi

metabolism
Proliferating Cell Nuclear Antigen

Protein Binding
metabolism
Xenopus Protein

DNA Replication
Chromatin Immunoprecipitation
Blotting
Western

genetics/metabolism
Chromatin Immunoprecipitation
Chromatin

DNA
Single-Stranded

Article
03 medical and health sciences
Minichromosome maintenance
ATP Binding Cassette Transporter
Subfamily B
Member 3

Proliferating Cell Nuclear Antigen
Animals
genetics/metabolism
Cell Cycle Protein

Molecular Biology
030304 developmental biology
DNA Helicases
DNA replication
Helicase
Minichromosome Maintenance Complex Component 2
genetics/metabolism
Mutation
Oocyte

biology.organism_classification
Molecular biology
GINS
enzymes and coenzymes (carbohydrates)
chemistry
Multiprotein Complexes
Mutation
Oocytes
biology.protein
Replisome
genetics/metabolism
Xenopus laevis

Rad51 Recombinase
Carrier Proteins
030217 neurology & neurosurgery
DNA
DNA Damage
Zdroj: Nature Structural & Molecular Biology
Nature structural & molecular biology
ISSN: 1545-9993
DOI: 10.1038/nsmb.2177
Popis: In higher eukaryotes the dynamics of replisome components during fork collapse and restart are poorly understood. Here, we reconstituted replication fork collapse and restart by inducing single-strand DNA (ssDNA) lesions that create a double-strand break (DSB) in one of the replicated sister chromatids after fork passage. We found that, upon fork collapse, the active CDC45–MCM–GINS (CMG) helicase complex loses its GINS subunit. A functional replisome is restored by the reloading of GINS and Pol epsilon onto DNA in a RAD51- and MRE11- dependent manner, but independently of replication origin assembly and firing. PCNA mutant alleles defective in break-induced replication (BIR) are unable to support restoration of replisome integrity. These results reveal that in higher eukaryotes replisomes are partially dismantled following fork collapse and fully re-established by a recombination-mediated process.
Databáze: OpenAIRE