Literature DB >> 8655587

Nuclear proteins of quiescent Xenopus laevis cells inhibit DNA replication in intact and permeabilized nuclei.

J Fang1, R M Benbow.   

Abstract

Quiescent cells from adult vertebrate liver and contact-inhibited or serum-deprived tissue cultures are active metabolically but do not carry out nuclear DNA replication and cell division. Replication of intact nuclei isolated from either quiescent Xenopus liver or cultured Xenopus A6 cells in quiescence was barely detectable in interphase extracts of Xenopus laevis eggs, although Xenopus sperm chromatin was replicated with approximately 100% efficiency in the same extracts. Permeabilization of nuclei from quiescent Xenopus liver or cultured Xenopus epithelial A6 cells did not facilitate efficient replication in egg extracts. Moreover, replication of Xenopus sperm chromatin in egg extracts was strongly inhibited by a soluble extract of isolated Xenopus liver nuclei; in contrast, complementary-strand synthesis on single-stranded DNA templates in egg extracts was not affected. Inhibition was specific to endogenous molecules localized preferentially in quiescent as opposed to proliferating cell nuclei, and was not due to suppression of cdk2 kinase activity. Extracts of Xenopus liver nuclei also inhibited growth of sperm nuclei formed in egg extracts. However, the rate and extent of decondensation of sperm chromatin in egg extracts were not affected. The formation of prereplication centers detected by anti-RP-A antibody was not affected by extracts of liver nuclei, but formation of active replication foci was blocked by the same extracts. Inhibition of DNA replication was alleviated when liver nuclear extracts were added to metaphase egg extracts before or immediately after Ca++ ion-induced transition to interphase. A plausible interpretation of our data is that endogenous inhibitors of DNA replication play an important role in establishing and maintaining a quiescent state in Xenopus cells, both in vivo and in cultured cells, perhaps by negatively regulating positive modulators of the replication machinery.

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Year:  1996        PMID: 8655587      PMCID: PMC2120854          DOI: 10.1083/jcb.133.5.955

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  69 in total

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Authors:  G Del Sal; M E Ruaro; L Philipson; C Schneider
Journal:  Cell       Date:  1992-08-21       Impact factor: 41.582

2.  FFA-1, a protein that promotes the formation of replication centers within nuclei.

Authors:  H Yan; J Newport
Journal:  Science       Date:  1995-09-29       Impact factor: 47.728

3.  Purification of an MCM-containing complex as a component of the DNA replication licensing system.

Authors:  J P Chong; H M Mahbubani; C Y Khoo; J J Blow
Journal:  Nature       Date:  1995-06-01       Impact factor: 49.962

4.  MCM3 complex required for cell cycle regulation of DNA replication in vertebrate cells.

Authors:  M A Madine; C Y Khoo; A D Mills; R A Laskey
Journal:  Nature       Date:  1995-06-01       Impact factor: 49.962

5.  Prokaryotic and eukaryotic replicons.

Authors:  J A Huberman
Journal:  Cell       Date:  1995-08-25       Impact factor: 41.582

6.  Visualization of replication factories attached to nucleoskeleton.

Authors:  P Hozák; A B Hassan; D A Jackson; P R Cook
Journal:  Cell       Date:  1993-04-23       Impact factor: 41.582

7.  Molecular cloning of a diverged homeobox gene that is rapidly down-regulated during the G0/G1 transition in vascular smooth muscle cells.

Authors:  D H Gorski; D F LePage; C V Patel; N G Copeland; N A Jenkins; K Walsh
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

8.  Association of human cyclin E with a periodic G1-S phase protein kinase.

Authors:  V Dulić; E Lees; S I Reed
Journal:  Science       Date:  1992-09-25       Impact factor: 47.728

9.  Identification of nuclear pre-replication centers poised for DNA synthesis in Xenopus egg extracts: immunolocalization study of replication protein A.

Authors:  Y Adachi; U K Laemmli
Journal:  J Cell Biol       Date:  1992-10       Impact factor: 10.539

10.  Initiation of DNA replication in nuclei from quiescent cells requires permeabilization of the nuclear membrane.

Authors:  G H Leno; R Munshi
Journal:  J Cell Biol       Date:  1994-10       Impact factor: 10.539

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  1 in total

1.  DNA replication in quiescent cell nuclei: regulation by the nuclear envelope and chromatin structure.

Authors:  Z H Lu; H Xu; G H Leno
Journal:  Mol Biol Cell       Date:  1999-12       Impact factor: 4.138

  1 in total

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