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Genome Maintenance by DNA Helicase B
- Source :
- Genes, Genes, Vol 11, Iss 578, p 578 (2020)
- Publication Year :
- 2020
- Publisher :
- MDPI AG, 2020.
-
Abstract
- DNA Helicase B (HELB) is a conserved helicase in higher eukaryotes with roles in the initiation of DNA replication and in the DNA damage and replication stress responses. HELB is a predominately nuclear protein in G1 phase where it is involved in initiation of DNA replication through interactions with DNA topoisomerase 2-binding protein 1 (TOPBP1), cell division control protein 45 (CDC45), and DNA polymerase α-primase. HELB also inhibits homologous recombination by reducing long-range end resection. After phosphorylation by cyclin-dependent kinase 2 (CDK2) at the G1 to S transition, HELB is predominately localized to the cytosol. However, this cytosolic localization in S phase is not exclusive. HELB has been reported to localize to chromatin in response to replication stress and to localize to the common fragile sites 16D (FRA16D) and 3B (FRA3B) and the rare fragile site XA (FRAXA) in S phase. In addition, HELB is phosphorylated in response to ionizing radiation and has been shown to localize to chromatin in response to various types of DNA damage, suggesting it has a role in the DNA damage response.
- Subjects :
- DNA Replication
0301 basic medicine
lcsh:QH426-470
DNA damage
DNA repair
DNA polymerase
Cell Cycle Proteins
DNA helicase
DNA Primase
Review
S Phase
03 medical and health sciences
0302 clinical medicine
Genetics
Humans
DNA Breaks, Double-Stranded
Phosphorylation
Homologous Recombination
Genetics (clinical)
biology
Genome, Human
Chemistry
Chromosome Fragile Sites
Topoisomerase
Cyclin-Dependent Kinase 2
DNA Helicases
DNA replication
Eukaryota
Nuclear Proteins
Helicase
DNA Polymerase I
genomic stability
G1 Phase Cell Cycle Checkpoints
Chromatin
Cell biology
DNA-Binding Proteins
lcsh:Genetics
030104 developmental biology
030220 oncology & carcinogenesis
biology.protein
Carrier Proteins
Homologous recombination
Subjects
Details
- ISSN :
- 20734425
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Genes
- Accession number :
- edsair.doi.dedup.....447938a87a04e032962fdd49e3f72f85