Affiliation:
1. Department of Biochemistry and Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871 Japan
Abstract
ABSTRACT
The
DPB11
gene, which genetically interacts with DNA polymerase II (ɛ), one of three replicative DNA polymerases, is required for DNA replication and the S phase checkpoint in
Saccharomyces cerevisiae
. To identify factors interacting with Dbp11, we have isolated
sld
(synthetically lethal with
dpb11-1
) mutations which fall into six complementation groups (
sld1
to -
6
). In this study, we characterized
SLD2
, encoding an essential 52-kDa protein. High-copy
SLD2
suppressed the thermosensitive growth defect caused by
dpb11-1
. Conversely, high-copy
DPB11
suppressed the temperature-sensitive growth defect caused by
sld2-6
. The interaction between Sld2 and Dpb11 was detected in a two-hybrid assay. This interaction was evident at 25°C but not at 34°C when Sld2-6 or Dpb11-1 replaced its wild-type protein. No interaction between Sld2-6 and Dpb11-1 could be detected even at 25°C. Immunoprecipitation experiments confirmed that Dpb11 physically interacts with Sld2.
sld2-6
cells were defective in DNA replication at the restrictive temperature, as were
dpb11-1
cells. Further, in
dpb11-1
and
sld2-6
cells, the bubble-shaped replication intermediates formed in the region of the autonomously replicating sequence reduced quickly after a temperature shift. These results strongly suggest the involvement of the Dpb11-Sld2 complex in a step close to the initiation of DNA replication.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
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