Isolation of the gene encoding yeast DNA polymerase I

A yeast genomic DNA expression library in λgt11 and 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 D...

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Veröffentlicht in:Cell 1985-11, Vol.43 (1), p.369-377
Hauptverfasser: Johnson, Lianna M., Snyder, Michael, Chang, Lucy M.S., Davis, Ronald W., Campbell, Judith L.
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Sprache:eng
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Zusammenfassung:A yeast genomic DNA expression library in λgt11 and 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.
ISSN:0092-8674
1097-4172
DOI:10.1016/0092-8674(85)90042-X