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PMID: 10693764 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The Saccharomyces Pif1p DNA helicase and the highly related Rrm3p have opposite effects on replication fork progression in ribosomal DNA.

Cell ·Vol. 100 ·No. 4 ·2000-02-18 ·Pages 479-89

Ivessa AS, Zhou JQ, Zakian VA

Abstract

Replication of Saccharomyces ribosomal DNA (rDNA) proceeds bidirectionally from origins in a subset of the approximately 150 tandem repeats, but the leftward-moving fork stops when it encounters the replication fork barrier (RFB). The Pif1p helicase and the highly related Rrm3p were rDNA associated in vivo. Both proteins affected rDNA replication but had opposing effects on fork progression. Pif1p helped maintain the RFB. Rrm3p appears to be the replicative helicase for rDNA as it acted catalytically to promote fork progression throughout the rDNA. Loss of Rrm3p increased rDNA breakage and accumulation of rDNA circles, whereas breakage and circles were less common in pif1 cells. These data support a model in which replication fork pausing causes breakage and recombination in the rDNA.

MeSH Terms
Amino Acid Sequence Base Sequence Catalysis DNA Helicases/genetics,metabolism DNA Replication DNA, Fungal/biosynthesis DNA, Ribosomal/biosynthesis DNA-Binding Proteins/metabolism Fungal Proteins/genetics,metabolism Molecular Sequence Data Rad52 DNA Repair and Recombination Protein Saccharomyces cerevisiae/enzymology,genetics Saccharomyces cerevisiae Proteins
Chemicals
DNA, Fungal DNA, Ribosomal DNA-Binding Proteins Fungal Proteins RAD52 protein, S cerevisiae Rad52 DNA Repair and Recombination Protein Saccharomyces cerevisiae Proteins PIF1 protein, S cerevisiae DNA Helicases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ivessa A S
Department of Molecular Biology, Princeton University, New Jersey 08544-1014, USA.
Zhou J Q
Zakian V A
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
2000-02-18
Pages
479-89
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM26938 · United States
Databases
GENBANK
U00062
PDB
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