MOLECULAR-CLONING, STRUCTURE AND EXPRESSION OF THE YEAST PROLIFERATING CELL NUCLEAR ANTIGEN GENE

被引:174
作者
BAUER, GA [1 ]
BURGERS, PMJ [1 ]
机构
[1] WASHINGTON UNIV, SCH MED, DEPT BIOCHEM & MOLEC BIOPHYS, ST LOUIS, MO 63110 USA
关键词
D O I
10.1093/nar/18.2.261
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The budding yeast Saccharomyces cerevisiae is proving to be an useful and accurate model for eukaryotic DNA replication. It contains both DNA polymerase α (I) and δ (III). Recently, proliferating cell nuclear antigen (PCNA), which in mammalian cells is an auxiliary subunit of DNA polymerase 6 and is essential for in vitro leading strand SV40 DNA replication, was purified from yeast. We have now cloned the gene for yeast PCNA (POL30). The gene codes for an essential protein of 29 kDa, which shows 35% homology with human PCNA. Cell cycle expression studies, using synchronized cells, show that expression of both the PCNA (POL30) and the DNA polymerase δ (POL3, or CDC2) genes of yeast are regulated in an identical fashion to that of the DNA polymerase a (POL1) gene. Thus, steady state mRNA levels increase 10-100-fold in late G1 phase, peak in early S-phase, and decrease to low levels in late Sphase. In addition, in meiosis mRNA levels increase prior to initiation of premeiotic DNA synthesis. © 1990 Oxford University Press.
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页码:261 / 265
页数:5
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