Home LiteratureArticle Details
PMID: 12944972 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex.

Nature ·Vol. 424 ·No. 6952 ·2003-08-28 ·Pages 1078-83

Katou Y, Kanoh Y, Bando M, Noguchi H, Tanaka H, Ashikari T, Sugimoto K, Shirahige K

Abstract

The checkpoint regulatory mechanism has an important role in maintaining the integrity of the genome. This is particularly important in S phase of the cell cycle, when genomic DNA is most susceptible to various environmental hazards. When chemical agents damage DNA, activation of checkpoint signalling pathways results in a temporary cessation of DNA replication. A replication-pausing complex is believed to be created at the arrested forks to activate further checkpoint cascades, leading to repair of the damaged DNA. Thus, checkpoint factors are thought to act not only to arrest replication but also to maintain a stable replication complex at replication forks. However, the molecular mechanism coupling checkpoint regulation and replication arrest is unknown. Here we demonstrate that the checkpoint regulatory proteins Tof1 and Mrc1 interact directly with the DNA replication machinery in Saccharomyces cerevisiae. When hydroxyurea blocks chromosomal replication, this assembly forms a stable pausing structure that serves to anchor subsequent DNA repair events.

MeSH Terms
Bromodeoxyuridine/metabolism Carrier Proteins/metabolism Cell Cycle Proteins/genetics,metabolism Chromosomes, Fungal/drug effects,metabolism DNA Replication/drug effects,genetics DNA-Binding Proteins Hydroxyurea/pharmacology Macromolecular Substances Mutation Nuclear Proteins/metabolism Oligonucleotide Array Sequence Analysis Protein Binding/drug effects S Phase/drug effects Saccharomyces cerevisiae/cytology,drug effects,genetics,metabolism Saccharomyces cerevisiae Proteins/genetics,metabolism
Chemicals
CDC45 protein, S cerevisiae Carrier Proteins Cell Cycle Proteins DNA-Binding Proteins MRC1 protein, S cerevisiae Macromolecular Substances Nuclear Proteins Saccharomyces cerevisiae Proteins TOF1 protein, S cerevisiae Bromodeoxyuridine Hydroxyurea
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Katou Yuki
Genome Structure and Function Team, Human Genome Research Group, RIKEN Genomic Science Center, 1-7-22 Suehiro-cho, Japan.
Kanoh Yutaka
Bando Masashige
Noguchi Hideki
Tanaka Hirokazu
Ashikari Toshihiko
Sugimoto Katsunori
Shirahige Katsuhiko
Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2003-08-28
Pages
1078-83
Language
English
Region
England
NLM ID
0410462
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com