Literature DB >> 7983177

Replication factories and nuclear bodies: the ultrastructural characterization of replication sites during the cell cycle.

P Hozák1, D A Jackson, P R Cook.   

Abstract

Sites of replication in synchronized HeLa cells were visualized by light and electron microscopy; cells were permeabilized and incubated with biotin-16-dUTP, and incorporation sites were immunolabelled. Electron microscopy of thick resinless sections from which approximately 90% chromatin had been removed showed that most DNA synthesis occurs in specific dense structures (replication factories) attached to a diffuse nucleoskeleton. These factories appear at the end of G1-phase and quickly become active; as S-phase progresses, they increase in size and decrease in number like sites of incorporation seen by light microscopy. Electron microscopy of conventional thin sections proved that these factories are a subset of nuclear bodies; they changed in the same characteristic way and contained DNA polymerase alpha and proliferating cell nuclear antigen. As replication factories can be observed and labelled in non-permeabilized cells, they cannot be aggregation artifacts. Some replication occurs outside factories at discrete sites on the diffuse skeleton; it becomes significant by mid S-phase and later becomes concentrated beneath the lamina.

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Year:  1994        PMID: 7983177     DOI: 10.1242/jcs.107.8.2191

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  47 in total

1.  hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci.

Authors:  H E Kleczkowska; G Marra; T Lettieri; J Jiricny
Journal:  Genes Dev       Date:  2001-03-15       Impact factor: 11.361

2.  Host DNA replication is induced by geminivirus infection of differentiated plant cells.

Authors:  Steven Nagar; Linda Hanley-Bowdoin; Dominique Robertson
Journal:  Plant Cell       Date:  2002-12       Impact factor: 11.277

3.  hMYH cell cycle-dependent expression, subcellular localization and association with replication foci: evidence suggesting replication-coupled repair of adenine:8-oxoguanine mispairs.

Authors:  I Boldogh; D Milligan; M S Lee; H Bassett; R S Lloyd; A K McCullough
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

4.  Distinct roles of the Adenovirus E4 ORF3 protein in viral DNA replication and inhibition of genome concatenation.

Authors:  Jared D Evans; Patrick Hearing
Journal:  J Virol       Date:  2003-05       Impact factor: 5.103

5.  Nucleoskeleton of early bovine embryos and differentiated somatic cells: an ultrastructural and immunocytochemical comparison.

Authors:  Jéril Degrouard; Pavel Hozák; Yvan Heyman; Jacques-Edmond Fléchon
Journal:  Histochem Cell Biol       Date:  2004-05-25       Impact factor: 4.304

6.  A cotranscriptional model for 3'-end processing of the Saccharomyces cerevisiae pre-ribosomal RNA precursor.

Authors:  Anthony K Henras; Edouard Bertrand; Guillaume Chanfreau
Journal:  RNA       Date:  2004-08-30       Impact factor: 4.942

7.  Activation of new replication foci under conditions of replication stress.

Authors:  P Rybak; A Waligórska; Ł Bujnowicz; A Hoang; J W Dobrucki
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

8.  Dimerization of simian virus 40 T-antigen hexamers activates T-antigen DNA helicase activity.

Authors:  N V Smelkova; J A Borowiec
Journal:  J Virol       Date:  1997-11       Impact factor: 5.103

9.  A geminivirus induces expression of a host DNA synthesis protein in terminally differentiated plant cells.

Authors:  S Nagar; T J Pedersen; K M Carrick; L Hanley-Bowdoin; D Robertson
Journal:  Plant Cell       Date:  1995-06       Impact factor: 11.277

10.  Cytology of DNA Replication Reveals Dynamic Plasticity of Large-Scale Chromatin Fibers.

Authors:  Xiang Deng; Oxana A Zhironkina; Varvara D Cherepanynets; Olga S Strelkova; Igor I Kireev; Andrew S Belmont
Journal:  Curr Biol       Date:  2016-08-25       Impact factor: 10.834

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