Literature DB >> 19563132

Determining the replication dynamics of specific gene loci by single-molecule analysis of replicated DNA.

Agnieszka Demczuk1, Paolo Norio.   

Abstract

In metazoans, development and cell differentiation are known to affect various aspects of chromosomal organization at developmentally regulated gene loci (e.g., nuclear localization, locus accessibility, chromatin modifications, etc.). Recent evidence also indicates that cell differentiation can have dramatic effects on DNA replication initiation and replication fork progression, at several of these loci. Hence, origin selection and activation are no longer viewed as constitutive events, but as actively regulated processes, the deregulation of which could potentially affect gene expression and genomic stability at particular chromosomal locations. For these reasons, the study of DNA replication across large genomic regions has recently received increasing attention. Here we describe an assay based on the analysis of single DNA molecules that can be used to determine the steady-state distribution of replication forks across large genomic regions. This assay can be used to study how DNA replication initiates, progresses, pauses, and terminates at single-copy loci in mammalian cells.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19563132     DOI: 10.1007/978-1-60327-815-7_35

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


  4 in total

1.  DNA fiber combing protocol using in-house reagents and coverslips to analyze replication fork dynamics in mammalian cells.

Authors:  Gemma Moore; Judit Jimenez Sainz; Ryan B Jensen
Journal:  STAR Protoc       Date:  2022-05-05

2.  Regulation of DNA replication within the immunoglobulin heavy-chain locus during B cell commitment.

Authors:  Agnieszka Demczuk; Michel G Gauthier; Ingrid Veras; Settapong Kosiyatrakul; Carl L Schildkraut; Meinrad Busslinger; John Bechhoefer; Paolo Norio
Journal:  PLoS Biol       Date:  2012-07-10       Impact factor: 8.029

3.  Replication fork slowing and stalling are distinct, checkpoint-independent consequences of replicating damaged DNA.

Authors:  Divya Ramalingam Iyer; Nicholas Rhind
Journal:  PLoS Genet       Date:  2017-08-14       Impact factor: 5.917

4.  CDK phosphorylation of SLD-2 is required for replication initiation and germline development in C. elegans.

Authors:  Vincent Gaggioli; Eva Zeiser; David Rivers; Charles R Bradshaw; Julie Ahringer; Philip Zegerman
Journal:  J Cell Biol       Date:  2014-02-17       Impact factor: 10.539

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.