Literature DB >> 14690605

The Saccharomyces cerevisiae helicase Rrm3p facilitates replication past nonhistone protein-DNA complexes.

Andreas S Ivessa1, Brian A Lenzmeier, Jessica B Bessler, Lara K Goudsouzian, Sandra L Schnakenberg, Virginia A Zakian.   

Abstract

The Saccharomyces cerevisiae RRM3 gene encodes a 5' to 3' DNA helicase. While replication of most of the yeast genome was not dependent upon Rrm3p, in its absence, replication forks paused and often broke at an estimated 1400 discrete sites, including tRNA genes, centromeres, inactive replication origins, and transcriptional silencers. These replication defects were associated with activation of the intra-S phase checkpoint. Activation of the checkpoint was critical for viability of rrm3Delta cells, especially at low temperatures. Each site whose replication was affected by Rrm3p is assembled into a nonnucleosomal protein-DNA complex. At tRNA genes and the silent mating type loci, disruption of these complexes eliminated dependence upon Rrm3p. These data indicate that the Rrm3p DNA helicase helps replication forks traverse protein-DNA complexes, naturally occurring impediments that are encountered in each S phase.

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Year:  2003        PMID: 14690605     DOI: 10.1016/s1097-2765(03)00456-8

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  234 in total

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4.  Replication stress checkpoint signaling controls tRNA gene transcription.

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5.  Fork rotation and DNA precatenation are restricted during DNA replication to prevent chromosomal instability.

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7.  The amino terminus of the Saccharomyces cerevisiae DNA helicase Rrm3p modulates protein function altering replication and checkpoint activity.

Authors:  Jessica B Bessler; Virginia A Zakian
Journal:  Genetics       Date:  2004-11       Impact factor: 4.562

Review 8.  Mechanism and physiological significance of programmed replication termination.

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Journal:  Semin Cell Dev Biol       Date:  2014-05-06       Impact factor: 7.727

Review 9.  Tus-Ter as a tool to study site-specific DNA replication perturbation in eukaryotes.

Authors:  Nicolai B Larsen; Ian D Hickson; Hocine W Mankouri
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

10.  Defects in DNA lesion bypass lead to spontaneous chromosomal rearrangements and increased cell death.

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