Literature DB >> 9821249

[Organization of DNA replication domains in S-phase nuclei of human cells].

L V Solovjeva1, A N Tomilin, Iu M Rozanov, N M Pleskach, V O Chagin, N V Tomilin.   

Abstract

Each chromosome of eukaryotic cells contains multiple units of DNA replication that are activated during S-phase of cell cycle according to a definite program. It is considered at present that the main independent units of replication in mammalian cells represent groups of 20-25 adjacent synchronously activated small (with the average size 100 kbp) replicons. After labelling of nascent DNA with nonradioactive DNA precursors and immunofluorescent staining of incorporated label, discrete replication domains (RDs) are detected in S-phase nuclei. It is assumed that each RD is formed by a single group of synchronously activated small replicons. Since the average rate of replication fork movement is 2 kbp/min, a group of small replicons should finish DNA synthesis within 25 min, and only during this time one RD should incorporate the replicative label. We have studied the duration of DNA synthesis in individual RDs in S-phase human cells using double replicative labelling that can be detected in the nucleus by specific reagents. Our results indicate that in the main fraction of RDs DNA synthesis lasts more than 90 min, that contradicts the generally accepted model of organization of replication units in mammalian cells (Hand, 1978), but is in agreement with an alternative model, according to which the main replication units are single or clustered big replicons more than 300 kbp in size (Liapunova, 1994).

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Year:  1998        PMID: 9821249

Source DB:  PubMed          Journal:  Tsitologiia        ISSN: 0041-3771


  2 in total

1.  Multiple deceleration of DNA synthesis during the S phase of cell cycle: study by flow cytometry method.

Authors:  V O Chagin; Yu M Rozanov; N V Tomilin
Journal:  Dokl Biochem Biophys       Date:  2004 Jan-Feb       Impact factor: 0.788

2.  A method to monitor replication fork progression in mammalian cells: nucleotide excision repair enhances and homologous recombination delays elongation along damaged DNA.

Authors:  Fredrik Johansson; Anne Lagerqvist; Klaus Erixon; Dag Jenssen
Journal:  Nucleic Acids Res       Date:  2004-11-10       Impact factor: 16.971

  2 in total

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