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Nucleotide excision repair of DNA in the yeast S. cerevisiae

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5269300

In the yeast S. cerevisiae the excision of pyrimidine dimers (produced by ultraviolet radiation) from DNA is apparently a complex biochemical process. Genetic studies indicate the involvement of at least 10 genes, 5 of which are absolutely required for the incision of DNA during excision repair. The authors have isolated these genes (RAD1, RAD2, RAD3, RAD4, RAD10) by molecular cloning. Sequencing has been completed on 4 of the genes and has provided information on the sizes of the proteins presumably encoded by them. In addition, regions of amino acid sequence homology with other proteins suggest evolutionary and functional relationships. To study aspects of the regulation of expression of these genes the authors have constructed RAD-lacZ fusions and have also quantitatively analyzed transcription of some of the RAD genes. These studies showed that the RAD2 gene undergoes enhanced transcription following exposure of cells to a variety of DNA damaging agents or agents which cause arrested DNA replication. The RAD1, RAD3, RAD4 and RAD10 genes are not induced under these conditions. Deletion analysis has shown that the RAD3 gene is essential for the viability of haploid yeast cells. Overexpression of the RAD3 and RAD2 genes in E. coli facilitated the raising of specific rabbit antisera to Rad3 and Rad2 proteins, and overexpression of the RAD3 gene in yeast has facilitated partial purification of Rad3 protein.

Research Organization:
Stanford Univ. School of Medicine, CA
OSTI ID:
5269300
Report Number(s):
CONF-8606151-
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Vol. 45:6; ISSN FEPRA
Country of Publication:
United States
Language:
English