New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells
DNA repair requires a coordinated effort from an array of factors that play different roles in the DNA damage response from recognizing and signaling the presence of a break, creating a repair competent environment, and physically repairing the lesion. Due to the rapid nature of many of these events...
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2021-09-01
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doaj-3ae1a349cef14eb090dbecb3b8d142b72021-09-13T05:25:14ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-09-01910.3389/fcell.2021.730998730998New Methodologies to Study DNA Repair Processes in Space and Time Within Living CellsSiham Zentout0Rebecca Smith1Marine Jacquier2Sébastien Huet3Sébastien Huet4Univ Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, BIOSIT-UMS 3480, Rennes, FranceUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, BIOSIT-UMS 3480, Rennes, FranceUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, BIOSIT-UMS 3480, Rennes, FranceUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, BIOSIT-UMS 3480, Rennes, FranceInstitut Universitaire de France, Paris, FranceDNA repair requires a coordinated effort from an array of factors that play different roles in the DNA damage response from recognizing and signaling the presence of a break, creating a repair competent environment, and physically repairing the lesion. Due to the rapid nature of many of these events, live-cell microscopy has become an invaluable method to study this process. In this review we outline commonly used tools to induce DNA damage under the microscope and discuss spatio-temporal analysis tools that can bring added information regarding protein dynamics at sites of damage. In particular, we show how to go beyond the classical analysis of protein recruitment curves to be able to assess the dynamic association of the repair factors with the DNA lesions as well as the target-search strategies used to efficiently find these lesions. Finally, we discuss how the use of mathematical models, combined with experimental evidence, can be used to better interpret the complex dynamics of repair proteins at DNA lesions.https://www.frontiersin.org/articles/10.3389/fcell.2021.730998/fullDNA damagelive cell imagingfluorescence fluctuation analysisspatio-temporal analysiskinetic modeling |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Siham Zentout Rebecca Smith Marine Jacquier Sébastien Huet Sébastien Huet |
spellingShingle |
Siham Zentout Rebecca Smith Marine Jacquier Sébastien Huet Sébastien Huet New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells Frontiers in Cell and Developmental Biology DNA damage live cell imaging fluorescence fluctuation analysis spatio-temporal analysis kinetic modeling |
author_facet |
Siham Zentout Rebecca Smith Marine Jacquier Sébastien Huet Sébastien Huet |
author_sort |
Siham Zentout |
title |
New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells |
title_short |
New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells |
title_full |
New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells |
title_fullStr |
New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells |
title_full_unstemmed |
New Methodologies to Study DNA Repair Processes in Space and Time Within Living Cells |
title_sort |
new methodologies to study dna repair processes in space and time within living cells |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cell and Developmental Biology |
issn |
2296-634X |
publishDate |
2021-09-01 |
description |
DNA repair requires a coordinated effort from an array of factors that play different roles in the DNA damage response from recognizing and signaling the presence of a break, creating a repair competent environment, and physically repairing the lesion. Due to the rapid nature of many of these events, live-cell microscopy has become an invaluable method to study this process. In this review we outline commonly used tools to induce DNA damage under the microscope and discuss spatio-temporal analysis tools that can bring added information regarding protein dynamics at sites of damage. In particular, we show how to go beyond the classical analysis of protein recruitment curves to be able to assess the dynamic association of the repair factors with the DNA lesions as well as the target-search strategies used to efficiently find these lesions. Finally, we discuss how the use of mathematical models, combined with experimental evidence, can be used to better interpret the complex dynamics of repair proteins at DNA lesions. |
topic |
DNA damage live cell imaging fluorescence fluctuation analysis spatio-temporal analysis kinetic modeling |
url |
https://www.frontiersin.org/articles/10.3389/fcell.2021.730998/full |
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