DNA damage induced during mitosis undergoes DNA repair synthesis

Autor: Veronica Gomez Godinez, Kyoko Yokomori, Sami Kabbara, José L. Maravillas-Montero, Michael W. Berns, Adria J. Sherman, Zhixia Shi, Daryl Preece, Shirli Cohen, Tao Wu, Xiangduo Kong
Přispěvatelé: Lustig, Arthur J
Jazyk: angličtina
Rok vydání: 2020
Předmět:
DNA Repair
ATM protein
adverse event
homologous recombination
animal cell
Biochemistry
0302 clinical medicine
genetics
Cell Cycle and Cell Division
histone H2AX
DNA strand breakage
0303 health sciences
nonhomologous end joining repair
protein function
Cell biology
Nucleic acids
Non-homologous end joining
Optical Equipment
030220 oncology & carcinogenesis
Medicine
Engineering and Technology
BRCA1 protein
radiation response
Infrared Rays
gamma H2AX
DNA damage
Science
Article
03 medical and health sciences
Potorous tridactylus
tumor suppressor p53 binding protein 1
ubiquitin
Genetics
Humans
human
Mitosis
anaphase
cell cycle G1 phase
potoroo
DNA synthesis
Lasers
human cell
DNA Breaks
G1 Phase
DNA
medicine.disease
Rad51 protein
laser
cell damage
Generic health relevance
nibrin
biosynthesis
rat kangaroo
animal
Multidisciplinary
DNA ligase IV
Chromosome Biology
cell line
unclassified drug
Cell Processes
DNA ligase
Interphase
Research Article
Premature aging
regulatory mechanism
General Science & Technology
DNA repair
Nucleic acid synthesis
Equipment
protein localization
Biology
discoidin domain receptor
metaphase
Non-Homologous End Joining
Cell Line
Potoroidae
medicine
Animals
double stranded DNA break
controlled study
Chemical synthesis
Metaphase
030304 developmental biology
nonhuman
Biology and life sciences
Cancer
Cell Biology
adverse device effect
Research and analysis methods
Biosynthetic techniques
infrared radiation
DNA repair synthesis
Zdroj: PloS one, vol 15, iss 4
PLoS ONE
PLoS ONE, Vol 15, Iss 4, p e0227849 (2020)
DOI: 10.1101/2020.01.03.893784
Popis: Understanding the mitotic DNA damage response (DDR) is critical to our comprehension of cancer, premature aging and developmental disorders which are marked by DNA repair deficiencies. In this study we use a micro-focused-laser to induce DNA damage in selected mitotic chromosomes to study the subsequent repair response. Our findings demonstrate that (1) mitotic cells are capable of DNA repair as evidenced by DNA synthesis at damage sites, (2) Repair is attenuated when DNA-PKcs and ATM are simultaneously compromised, (3) Laser damage may permit the observation of previously undetected DDR proteins when damage is elicited by other methods in mitosis, and (4) Twenty five percent of mitotic DNA-damaged cells undergo a subsequent mitosis. Together these findings suggest that mitotic DDR is more complex than previously thought and may involve factors from multiple repair pathways that are better understood in interphase.
Databáze: OpenAIRE