Role of a complex containing Rad17, Mec3, and Ddc1 in the yeast DNA damage checkpoint pathway

Tae Kondo, Kunihiro Matsumoto, Katsunori Sugimoto

Research output: Contribution to journalArticle

107 Citations (Scopus)

Abstract

Genetic analysis has suggested that RAD17, RAD24, MEC3, and DDC1 play similar roles in the DNA damage checkpoint control in budding yeast. These genes are required for DNA damage-induced Rad53 phosphorylation and considered to function upstream of RAD53 in the DNA damage checkpoint pathway. Here we identify Mec3 as a protein that associates with Rad17 in a two-hybrid screen and demonstrate that Rad17 and Mec3 interact physically in vivo. The amino terminus of Rad17 is required for its interaction with Mec3, and the protein encoded by the rad17-1 allele, containing a missense mutation at the amino terminus, is defective for its interaction with Mec3 in vivo. Ddc1 interacts physically and cosediments with both Rad17 and Mec3, indicating that these three proteins form a complex. On the other hand, Rad24 is not found to associate with Rad17, Mec3, and Ddc1. DDC1 overexpression can partially suppress the phenotypes of the rad24Δ mutation: sensitivity to DNA damage, defect in the DNA damage checkpoint and decrease in DNA damage- induced phosphorylation of Rad53. Taken together, our results suggest that Rad17, Mec3, and Ddc1 form a complex which functions downstream of Rad24 in the DNA damage checkpoint pathway.

Original languageEnglish (US)
Pages (from-to)1136-1143
Number of pages8
JournalMolecular and cellular biology
Volume19
Issue number2
DOIs
StatePublished - Jan 1 1999

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DNA Damage
Yeasts
Phosphorylation
Proteins
Saccharomycetales
Missense Mutation
Alleles
Phenotype
Mutation
Genes

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Cell Biology

Cite this

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title = "Role of a complex containing Rad17, Mec3, and Ddc1 in the yeast DNA damage checkpoint pathway",
abstract = "Genetic analysis has suggested that RAD17, RAD24, MEC3, and DDC1 play similar roles in the DNA damage checkpoint control in budding yeast. These genes are required for DNA damage-induced Rad53 phosphorylation and considered to function upstream of RAD53 in the DNA damage checkpoint pathway. Here we identify Mec3 as a protein that associates with Rad17 in a two-hybrid screen and demonstrate that Rad17 and Mec3 interact physically in vivo. The amino terminus of Rad17 is required for its interaction with Mec3, and the protein encoded by the rad17-1 allele, containing a missense mutation at the amino terminus, is defective for its interaction with Mec3 in vivo. Ddc1 interacts physically and cosediments with both Rad17 and Mec3, indicating that these three proteins form a complex. On the other hand, Rad24 is not found to associate with Rad17, Mec3, and Ddc1. DDC1 overexpression can partially suppress the phenotypes of the rad24Δ mutation: sensitivity to DNA damage, defect in the DNA damage checkpoint and decrease in DNA damage- induced phosphorylation of Rad53. Taken together, our results suggest that Rad17, Mec3, and Ddc1 form a complex which functions downstream of Rad24 in the DNA damage checkpoint pathway.",
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Role of a complex containing Rad17, Mec3, and Ddc1 in the yeast DNA damage checkpoint pathway. / Kondo, Tae; Matsumoto, Kunihiro; Sugimoto, Katsunori.

In: Molecular and cellular biology, Vol. 19, No. 2, 01.01.1999, p. 1136-1143.

Research output: Contribution to journalArticle

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