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DNA replication profiling by molecular combing on single DNA fibers

In this protocol, the progression of DNA synthesis is profiled at a single-molecule resolution. DNA fibers are uniformly stretched on silanized coverslips, and replicating DNA can be traced with thymidine analogs using specific antibodies against distinct analogs. Single DNA fibers are visualized by...

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Detalles Bibliográficos
Autores principales: Fu, Haiqing, Aladjem, Mirit I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026583/
https://www.ncbi.nlm.nih.gov/pubmed/35463463
http://dx.doi.org/10.1016/j.xpro.2022.101290
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author Fu, Haiqing
Aladjem, Mirit I.
author_facet Fu, Haiqing
Aladjem, Mirit I.
author_sort Fu, Haiqing
collection PubMed
description In this protocol, the progression of DNA synthesis is profiled at a single-molecule resolution. DNA fibers are uniformly stretched on silanized coverslips, and replicating DNA can be traced with thymidine analogs using specific antibodies against distinct analogs. Single DNA fibers are visualized by an anti-single stranded DNA antibody. The protocol can be used to study DNA replication dynamics, the cellular response to replication stress, and replication fork progression at specific chromosomal regions when combined with fluorescent in situ hybridization. For complete details on the use and execution of this protocol, please refer to Conti et al. (2007), Fu et al. (2021), Kaykov et al. (2016), Redmond et al. (2018), and Schwob et al. (2009).
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spelling pubmed-90265832022-04-23 DNA replication profiling by molecular combing on single DNA fibers Fu, Haiqing Aladjem, Mirit I. STAR Protoc Protocol In this protocol, the progression of DNA synthesis is profiled at a single-molecule resolution. DNA fibers are uniformly stretched on silanized coverslips, and replicating DNA can be traced with thymidine analogs using specific antibodies against distinct analogs. Single DNA fibers are visualized by an anti-single stranded DNA antibody. The protocol can be used to study DNA replication dynamics, the cellular response to replication stress, and replication fork progression at specific chromosomal regions when combined with fluorescent in situ hybridization. For complete details on the use and execution of this protocol, please refer to Conti et al. (2007), Fu et al. (2021), Kaykov et al. (2016), Redmond et al. (2018), and Schwob et al. (2009). Elsevier 2022-04-12 /pmc/articles/PMC9026583/ /pubmed/35463463 http://dx.doi.org/10.1016/j.xpro.2022.101290 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Fu, Haiqing
Aladjem, Mirit I.
DNA replication profiling by molecular combing on single DNA fibers
title DNA replication profiling by molecular combing on single DNA fibers
title_full DNA replication profiling by molecular combing on single DNA fibers
title_fullStr DNA replication profiling by molecular combing on single DNA fibers
title_full_unstemmed DNA replication profiling by molecular combing on single DNA fibers
title_short DNA replication profiling by molecular combing on single DNA fibers
title_sort dna replication profiling by molecular combing on single dna fibers
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026583/
https://www.ncbi.nlm.nih.gov/pubmed/35463463
http://dx.doi.org/10.1016/j.xpro.2022.101290
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