| Literature DB >> 3907855 |
L M Johnson, M Snyder, L M Chang, R W Davis, J L Campbell.
Abstract
A yeast genomic DNA expression library in lambda gt11 antibody prepared against yeast DNA polymerase I were used to isolate the gene encoding DNA polymerase I. The identity of the DNA polymerase I gene was determined by several criteria. First, the clone-encoded protein is immunologically related to DNA polymerase I. Second, cells containing the gene cloned in the high copy number plasmid YEp24 overproduce the polymerase activity 4- to 5-fold as measured in yeast extracts. Finally, insertion of the gene downstream from a bacteriophage T7 promoter allows synthesis of yeast DNA polymerase I in Escherichia coli. Gene disruption and Southern hybridization experiments show that the polymerase is encoded by an essential, single copy gene. Examination of the germinated spores containing the disrupted gene reveals a defect in nuclear division and a terminal phenotype typical of replication mutants.Entities:
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Year: 1985 PMID: 3907855 DOI: 10.1016/0092-8674(85)90042-x
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582