Literature DB >> 35290633

Studying Single-Stranded DNA Gaps at Replication Intermediates by Electron Microscopy.

Jessica Jackson1, Alessandro Vindigni2.   

Abstract

Single-stranded DNA gaps are frequent structures that accumulate on newly synthesized DNA under conditions of replication stress. The identification of these single-stranded DNA gaps has been instrumental to uncover the mechanisms that allow the DNA replication machinery to skip intrinsic replication obstacles or DNA lesions. DNA fiber assays provide an essential tool for detecting perturbations in DNA replication fork dynamics genome-wide at single molecule resolution along with identifying the presence of single-stranded gaps when used in combination with S1 nuclease. However, electron microscopy is the only technique allowing the actual visualization and localization of single-stranded DNA gaps on replication forks. This chapter provides a detailed method for visualizing single-stranded DNA gaps at the replication fork by electron microscopy including psoralen cross-linking of cultured mammalian cells, extraction of genomic DNA, and finally enrichment of replication intermediates followed by spreading and platinum rotary shadowing of the DNA onto grids. Discussion on identification and analysis of these gaps as well as on the advantages and disadvantages of electron microscopy relative to the DNA fiber technique is also included.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  DNA replication; DNA replication stress; Electron microscopy; Replication structures; ssDNA gaps

Mesh:

Substances:

Year:  2022        PMID: 35290633     DOI: 10.1007/978-1-0716-2063-2_6

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


  24 in total

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Authors:  Massimo Lopes; Marco Foiani; José M Sogo
Journal:  Mol Cell       Date:  2006-01-06       Impact factor: 17.970

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Authors:  Silvana Mourón; Sara Rodriguez-Acebes; María I Martínez-Jiménez; Sara García-Gómez; Sandra Chocrón; Luis Blanco; Juan Méndez
Journal:  Nat Struct Mol Biol       Date:  2013-11-17       Impact factor: 15.369

4.  hPrimpol1/CCDC111 is a human DNA primase-polymerase required for the maintenance of genome integrity.

Authors:  Li Wan; Jiangman Lou; Yisui Xia; Bei Su; Ting Liu; Jiamin Cui; Yingying Sun; Huiqiang Lou; Jun Huang
Journal:  EMBO Rep       Date:  2013-10-15       Impact factor: 8.807

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Journal:  Science       Date:  1994-09-30       Impact factor: 47.728

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Authors:  A R Lehmann
Journal:  Eur J Biochem       Date:  1972-12-18

7.  UV stalled replication forks restart by re-priming in human fibroblasts.

Authors:  Ingegerd Elvers; Fredrik Johansson; Petra Groth; Klaus Erixon; Thomas Helleday
Journal:  Nucleic Acids Res       Date:  2011-06-06       Impact factor: 16.971

8.  DNA damage bypass operates in the S and G2 phases of the cell cycle and exhibits differential mutagenicity.

Authors:  Noam Diamant; Ayal Hendel; Ilan Vered; Thomas Carell; Thomas Reissner; Niels de Wind; Nicholas Geacinov; Zvi Livneh
Journal:  Nucleic Acids Res       Date:  2011-09-09       Impact factor: 16.971

9.  PrimPol, an archaic primase/polymerase operating in human cells.

Authors:  Sara García-Gómez; Aurelio Reyes; María I Martínez-Jiménez; E Sandra Chocrón; Silvana Mourón; Gloria Terrados; Christopher Powell; Eduardo Salido; Juan Méndez; Ian J Holt; Luis Blanco
Journal:  Mol Cell       Date:  2013-10-24       Impact factor: 17.970

10.  PrimPol bypasses UV photoproducts during eukaryotic chromosomal DNA replication.

Authors:  Julie Bianchi; Sean G Rudd; Stanislaw K Jozwiakowski; Laura J Bailey; Violetta Soura; Elaine Taylor; Irena Stevanovic; Andrew J Green; Travis H Stracker; Howard D Lindsay; Aidan J Doherty
Journal:  Mol Cell       Date:  2013-11-21       Impact factor: 17.970

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