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Cellular Assays to Study the Functional Importance of Human DNA Repair Helicases
- Source :
- Methods Mol Biol, Methods in Molecular Biology ISBN: 9781493994991
- Publication Year :
- 2019
-
Abstract
- DNA helicases represent a specialized class of enzymes that play crucial roles in the DNA damage response. Using the energy of nucleoside triphosphate binding and hydrolysis, helicases behave as molecular motors capable of efficiently disrupting the many noncovalent hydrogen bonds that stabilize DNA molecules with secondary structure. In addition to their importance in DNA damage sensing and signaling, DNA helicases facilitate specific steps in DNA repair mechanisms that require polynucleotide tract unwinding or resolution. Because they play fundamental roles in the DNA damage response and DNA repair, defects in helicases disrupt cellular homeostasis. Thus, helicase deficiency or inhibition may result in reduced cell proliferation and survival, apoptosis, DNA damage induction, defective localization of repair proteins to sites of genomic DNA damage, chromosomal instability, and defective DNA repair pathways such as homologous recombination of double-strand breaks. In this chapter, we will describe step-by-step protocols to assay the functional importance of human DNA repair helicases in genome stability and cellular homeostasis.
- Subjects :
- 0301 basic medicine
DNA Repair
DNA repair
DNA damage
Cellular homeostasis
Apoptosis
Cell Count
Genomic Instability
Article
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Cell Line, Tumor
Humans
Cell Proliferation
Enzyme Assays
biology
Chemistry
DNA Helicases
Helicase
Cell biology
genomic DNA
030104 developmental biology
Microscopy, Fluorescence
Polynucleotide
030220 oncology & carcinogenesis
biology.protein
Biological Assay
Homologous recombination
DNA
Subjects
Details
- ISBN :
- 978-1-4939-9499-1
- ISSN :
- 19406029
- ISBNs :
- 9781493994991
- Volume :
- 1999
- Database :
- OpenAIRE
- Journal :
- Methods in molecular biology (Clifton, N.J.)
- Accession number :
- edsair.doi.dedup.....8a660f0ad1682d5ea562b180a5b9fdf7