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Published on: May 31, 2011
Analysis on origin recognition complex containing Orc5p with defective Walker A motif
Naoko Takahashi1, Yoshihiro Yamaguchi, Fumiko Yamairi
1Faculty of Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.
Abstract:
Orc5p is one of six proteins that make up the origin recognition complex (ORC), a candidate initiator of chromosomal DNA replication in eukaryotes. To investigate the role of ATP binding to Orc5p in cells, we constructed orc5-A, a strain of Saccharomyces cerevisiae having a mutation in the Walker A motif of Orc5p (K43E). The strain showed temperature-sensitive growth. Incubation at a nonpermissive temperature (37 degrees C) caused accumulation of cells with nearly 2C DNA content. Overproduction of Orc4p, another subunit of ORC, suppresses this temperature sensitivity, but overproduction of other subunits did not. Overproduction of Orc4p did not suppress the temperature sensitivity of another orc5 mutant, orc5-1, whose mutation, L331P, is outside the ATP-binding motif. These results suggest that Orc4p is specifically involved in ATP binding to Orc5p itself or its function in DNA replication. Immunoblotting experiments revealed that in the orc5-A strain at a nonpermissive temperature, all ORC subunits gradually disappeared, suggesting that ORC5-A becomes degraded at nonpermissive temperatures. We therefore consider that ATP binding to Orc5p is involved in efficient ORC formation and that Orc4p is involved in this process.
Insights
ATP binding to Orc5p is crucial for the origin recognition complex (ORC) formation and function in DNA replication. Orc4p specifically aids Orc5p
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- The origin recognition complex (ORC) initiates eukaryotic chromosomal DNA replication.
- Orc5p is a key subunit of the ORC.
Purpose of the Study:
- To investigate the role of ATP binding to Orc5p in Saccharomyces cerevisiae.
- To determine the specific function of Orc4p in Orc5p-mediated processes.
Main Methods:
- Construction of an orc5-A mutant strain with a defective Walker A motif in Orc5p.
- Temperature-shift experiments to assess growth and DNA content.
- Overexpression of ORC subunits to identify suppressors.
- Immunoblotting to analyze ORC subunit stability.
Main Results:
- The orc5-A mutation caused temperature-sensitive growth and DNA replication defects.
- Overproduction of Orc4p, but not other ORC subunits, suppressed the temperature sensitivity.
- Orc4p overexpression did not rescue a distinct orc5 mutant (orc5-1).
- ORC subunits were degraded in the orc5-A strain at nonpermissive temperatures.
Conclusions:
- ATP binding to Orc5p is essential for stable ORC formation and efficient DNA replication initiation.
- Orc4p plays a specific role in supporting Orc5p's ATP binding or function.
- Orc5p's ATP-binding capability is critical for ORC assembly and stability.
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