Literature DB >> 36066713

DNA Damage Foci on Metaphase Chromosomes.

Takamitsu A Kato1.   

Abstract

After DNAs are damaged, DNA repair proteins accumulate and are activated at the DNA damaged site. These accumulated proteins are visualized as foci by fluorescent immunocytochemistry technique. This allows the DNA damage responses in interphase nuclei to be detected; it was earlier times difficult to analyze DNA damage in situ. In order to analyze DNA damage in interphase cells, either DNA is extracted to assay breaks biochemically, or premature chromosome condensation is conducted to observe as chromatin breaks. Although DNA damage-induced foci are typically analyzed in interphase cells, these foci can be also visualized on mitotic chromosomes. The foci where the repair proteins accumulate at the damage site is observed as mitotic chromosome break site. Since mitotic cells attach loosely or not attached to cell culture vessels, it is difficult to analyze foci on chromosomes in culture vessels under a microscope, so metaphase chromosome spread must be prepared for accurate analysis. The cytocentrifuge system is an ideal method to adhere mitotic cells to microscope slides for the fluorescent immunocytochemistry. This chapter introduces cytocentrifuge method to prepare metaphase spread for DNA damage foci analysis.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cytocentrifugation; DNA damage foci; Fluorescent immunocytochemistry

Mesh:

Substances:

Year:  2023        PMID: 36066713     DOI: 10.1007/978-1-0716-2433-3_10

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  14 in total

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Authors:  S S Yuan; S Y Lee; G Chen; M Song; G E Tomlinson; E Y Lee
Journal:  Cancer Res       Date:  1999-08-01       Impact factor: 12.701

2.  Ataxia telangiectasia mutated (ATM) kinase and ATM and Rad3 related kinase mediate phosphorylation of Brca1 at distinct and overlapping sites. In vivo assessment using phospho-specific antibodies.

Authors:  M Gatei; B B Zhou; K Hobson; S Scott; D Young; K K Khanna
Journal:  J Biol Chem       Date:  2001-02-13       Impact factor: 5.157

3.  ATR and ATM-dependent movement of BLM helicase during replication stress ensures optimal ATM activation and 53BP1 focus formation.

Authors:  Albert R Davalos; Patrick Kaminker; Rhonda K Hansen; Judith Campisi
Journal:  Cell Cycle       Date:  2004-12-04       Impact factor: 4.534

4.  Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells.

Authors:  M A Siddique; K Nakanishi; T Taniguchi; M Grompe; A D D'Andrea
Journal:  Exp Hematol       Date:  2001-12       Impact factor: 3.084

5.  hMre11 and hRad50 nuclear foci are induced during the normal cellular response to DNA double-strand breaks.

Authors:  R S Maser; K J Monsen; B E Nelms; J H Petrini
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

6.  Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway.

Authors:  I Garcia-Higuera; T Taniguchi; S Ganesan; M S Meyn; C Timmers; J Hejna; M Grompe; A D D'Andrea
Journal:  Mol Cell       Date:  2001-02       Impact factor: 17.970

7.  ATM-dependent phosphorylation of nibrin in response to radiation exposure.

Authors:  M Gatei; D Young; K M Cerosaletti; A Desai-Mehta; K Spring; S Kozlov; M F Lavin; R A Gatti; P Concannon; K Khanna
Journal:  Nat Genet       Date:  2000-05       Impact factor: 38.330

8.  Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes.

Authors:  T Haaf; E I Golub; G Reddy; C M Radding; D C Ward
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-14       Impact factor: 11.205

9.  Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrest.

Authors:  Annapaola Franchitto; Pietro Pichierri
Journal:  J Cell Biol       Date:  2002-03-26       Impact factor: 10.539

10.  p53 binding protein 1 (53BP1) is an early participant in the cellular response to DNA double-strand breaks.

Authors:  L B Schultz; N H Chehab; A Malikzay; T D Halazonetis
Journal:  J Cell Biol       Date:  2000-12-25       Impact factor: 10.539

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