Literature DB >> 8044842

Two steps in the assembly of complexes at yeast replication origins in vivo.

J F Diffley1, J H Cocker, S J Dowell, A Rowley.   

Abstract

The integration of chromosomal DNA replication into the eukaryotic cell cycle might involve temporal regulation of interactions between cellular factors and replication origins. We show here that yeast replication origins exist in two chromatin states during the cell cycle. In the postreplicative state, genomic footprints closely resemble those produced in vitro by the purified ORC and ABF1 proteins, indicating that the binding of these proteins to replication origins is not sufficient to drive the initiation of DNA replication. The prereplicative state is characterized by an additional region of protection overlapping the ORC footprint. This prereplicative complex appears near the end of mitosis and persists through G1. After entry into S phase, origins return to the postreplicative state. Similarities in temporal regulation of the prereplicative state and the Xenopus licensing factor suggest that mechanisms limiting DNA replication to once per cell cycle may be conserved among eukaryotes.

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Year:  1994        PMID: 8044842     DOI: 10.1016/0092-8674(94)90299-2

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  223 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

2.  Association of fission yeast Orp1 and Mcm6 proteins with chromosomal replication origins.

Authors:  Y Ogawa; T Takahashi; H Masukata
Journal:  Mol Cell Biol       Date:  1999-10       Impact factor: 4.272

3.  Dbf4p, an essential S phase-promoting factor, is targeted for degradation by the anaphase-promoting complex.

Authors:  M F Ferreira; C Santocanale; L S Drury; J F Diffley
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

4.  Functionally distinct, sequence-specific replicator and origin elements are required for Drosophila chorion gene amplification.

Authors:  L Lu; H Zhang; J Tower
Journal:  Genes Dev       Date:  2001-01-15       Impact factor: 11.361

5.  A fission yeast gene, him1(+)/dfp1(+), encoding a regulatory subunit for Hsk1 kinase, plays essential roles in S-phase initiation as well as in S-phase checkpoint control and recovery from DNA damage.

Authors:  T Takeda; K Ogino; E Matsui; M K Cho; H Kumagai; T Miyake; K Arai; H Masai
Journal:  Mol Cell Biol       Date:  1999-08       Impact factor: 4.272

6.  Differential assembly of Cdc45p and DNA polymerases at early and late origins of DNA replication.

Authors:  O M Aparicio; A M Stout; S P Bell
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

7.  An origin of bidirectional DNA replication is located within a CpG island at the 3" end of the chicken lysozyme gene.

Authors:  L Phi-van; W H Strätling
Journal:  Nucleic Acids Res       Date:  1999-08-01       Impact factor: 16.971

8.  Cell cycle control of Cdc7p kinase activity through regulation of Dbf4p stability.

Authors:  G Oshiro; J C Owens; Y Shellman; R A Sclafani; J J Li
Journal:  Mol Cell Biol       Date:  1999-07       Impact factor: 4.272

9.  Assembly of a complex containing Cdc45p, replication protein A, and Mcm2p at replication origins controlled by S-phase cyclin-dependent kinases and Cdc7p-Dbf4p kinase.

Authors:  L Zou; B Stillman
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

10.  DNA repair in a yeast origin of replication: contributions of photolyase and nucleotide excision repair.

Authors:  B Suter; R E Wellinger; F Thoma
Journal:  Nucleic Acids Res       Date:  2000-05-15       Impact factor: 16.971

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