Purification of the cdc8 protein of Saccharomyces cerevisiae by complementation in an aphidicolin-sensitive in vitro DNA replication system
- Creators
- Kuo, Chia-Lam
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Campbell, Judith L.
Abstract
DNA synthesis in vitro in Brij-treated Saccharomyces cerevisiae requires the product of the CDC8 gene (Hereford, L. M. & Hartwell, L. H. (1971) Nature (London) New Biol. 234, 171-172). Extracts of wild-type A364a yeast restore DNA synthesis in Brij-treated cdc8, a mutant containing a thermolabile cdc8 gene product. This constitutes a complementation assay by which the cdc8 gene product can be monitored during purification. A heat-stable protein responsible for this complementation has been partially purified from both wild-type A364a cells and from a cdc8 temperature-sensitive mutant. The complementation activity from the mutant is thermolabile when compared to the wild-type activity, indicating that CDC8 is the structural gene for the protein.
Additional Information
© 1982 by the National Academy of Sciences. Communicated by Norman Davidson, July 27, 1981. We thank S.E. Celniker for helpful discussion. This investigation was supported by U.S. Public Health Service Grant GM 25508 and Research Career Development Award CA 00544. The publication costs of this article were defrayed in part by page charge payment. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.Attached Files
Published - KUOpnas82.pdf
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Additional details
- PMCID
- PMC346646
- Eprint ID
- 8572
- Resolver ID
- CaltechAUTHORS:KUOpnas82
- NIH
- GM 25508
- NIH
- CA 00544
- Created
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2007-08-21Created from EPrint's datestamp field
- Updated
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2019-10-02Created from EPrint's last_modified field