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RECQ1 plays a distinct role in cellular response to oxidative DNA damage.
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title
RECQ1 plays a distinct role in cellular response to oxidative DNA damage
(English)
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3420015
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30 January 2020
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DNA damage
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Sudha Sharma
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1
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30 January 2020
Jeannine R LaRocque
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5
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Pornima Phatak
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30 January 2020
Alexei Stortchevoi
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30 January 2020
Maria Jasin
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4
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publication date
26 April 2012
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30 January 2020
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DNA Repair
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11
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30 January 2020
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6
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30 January 2020
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537-549
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30 January 2020
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PARP-1 enhances the mismatch-dependence of 5'-directed excision in human mismatch repair in vitro
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Poly (ADP-ribose) polymerase (PARP) is not involved in base excision repair but PARP inhibition traps a single-strand intermediate
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FANCJ helicase uniquely senses oxidative base damage in either strand of duplex DNA and is stimulated by replication protein A to unwind the damaged DNA substrate in a strand-specific manner
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RecQ4 facilitates UV light-induced DNA damage repair through interaction with nucleotide excision repair factor xeroderma pigmentosum group A (XPA)
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RECQ1 helicase interacts with human mismatch repair factors that regulate genetic recombination
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DNA damage responses to oxidative stress
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1 October 2017
Analysis of the unwinding activity of the dimeric RECQ1 helicase in the presence of human replication protein A
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1 October 2017
Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage
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A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage
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Characterization of the DNA-unwinding activity of human RECQ1, a helicase specifically stimulated by human replication protein A.
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Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrest
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The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA.
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The contribution of endogenous sources of DNA damage to the multiple mutations in cancer
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1 October 2017
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1 October 2017
Repair of double-strand breaks by homologous recombination in mismatch repair-defective mammalian cells
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ATP depletion + pyrimidine depletion can markedly enhance cancer therapy: fresh insight for a new approach
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Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations
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Werner helicase is localized to transcriptionally active nucleoli of cycling cells
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Nucleolar localization of the Werner syndrome protein in human cells
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XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage
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Cloning of a cDNA encoding a novel importin-alpha homologue, Qip1: discrimination of Qip1 and Rch1 from hSrp1 by their ability to interact with DNA helicase Q1/RecQL
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Repair of products of oxidative DNA base damage in human cells
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Post-translational modification of poly(ADP-ribose) polymerase induced by DNA strand breaks
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Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ
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Free radicals in biology: oxidative stress and the effects of ionizing radiation
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Chromosomal localization of the gene encoding the human DNA helicase RECQL and its mouse homologue
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
retrieved
1 October 2017
Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
retrieved
1 October 2017
Altered temporal expression of DNA repair in hypermutable Bloom's syndrome cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
retrieved
1 October 2017
The kinetics of repair of oxidative DNA damage (strand breaks and oxidised pyrimidines) in human cells.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
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2 July 2018
Deoxyribonucleic acid-protein and deoxyribonucleic acid interstrand cross-links induced in isolated chromatin by hydrogen peroxide and ferrous ethylenediaminetetraacetate chelates
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
retrieved
2 July 2018
The Human RecQ helicases, BLM and RECQ1, display distinct DNA substrate specificities.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
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23 September 2018
RECQL4-deficient cells are hypersensitive to oxidative stress/damage: Insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
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23 September 2018
Nuclear retention of ATM at sites of DNA double strand breaks
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420015
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23 September 2018
Elevated superoxide dismutase in Bloom's syndrome: a genetic condition of oxidative stress
1 reference
stated in
PubMed
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https://pubmed.ncbi.nlm.nih.gov/22542292
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Werner syndrome cells escape hydrogen peroxide-induced cell proliferation arrest
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22542292
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22542292
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Multiple involvement of oxidative stress in Werner syndrome phenotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22542292
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.DNAREP.2012.04.003
1 reference
stated in
Europe PubMed Central
PMC publication ID
3420015
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22542292%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
PMC publication ID
3420015
1 reference
stated in
Europe PubMed Central
PMC publication ID
3420015
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22542292%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
PubMed publication ID
22542292
1 reference
stated in
Europe PubMed Central
PMC publication ID
3420015
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22542292%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
ResearchGate publication ID
224866080
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