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Molecular and Cellular Biology, February 1999, p. 1136-1143, Vol. 19, No. 2
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Role of a Complex Containing Rad17, Mec3, and
Ddc1 in the Yeast DNA Damage Checkpoint Pathway
Tae
Kondo,
Kunihiro
Matsumoto,* and
Katsunori
Sugimoto
Division of Biological Science, Graduate
School of Science, Nagoya University, Chikusa-ku, Nagoya 464-0814, Japan
Received 3 August 1998/Returned for modification 15 September
1998/Accepted 12 November 1998
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 rad24
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.
*
Corresponding author. Mailing address: Division of
Biological Science, Graduate School of Science, Nagoya University,
Chikusa-ku, Nagoya 464-0814, Japan. Phone: 81-52-789-2593. Fax:
81-52-789-2589.
Molecular and Cellular Biology, February 1999, p. 1136-1143, Vol. 19, No. 2
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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