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Mol. Cell. Biol., Feb 1997, 635-643, Vol 17, No. 2
Z Wang, S Wei, SH Reed, X Wu, JQ Svejstrup, WJ Feaver, RD Kornberg and EC Friedberg
Nucleotide excision repair (NER) is a biochemical process required for the
repair of many different types of DNA lesions. In the yeast Saccharomyces
cerevisiae, the RAD7, RAD16, and RAD23 genes have been specifically
implicated in NER of certain transcriptionally repressed loci and in the
nontranscribed strand of transcriptionally active genes. We have used a
cell-free system to study the roles of the Rad7, Rad16, and Rad23 proteins
in NER. Transcription-independent NER of a plasmid substrate was defective
in rad7, rad16, and rad23 mutant extracts. Complementation studies with a
previously purified NER protein complex (nucleotide excision repairosome)
indicate that Rad23 is a component of the repairosome, whereas Rad7 and
Rad16 proteins were not found in this complex. Complementation studies with
rad4, rad7, rad16, and rad23 mutant extracts suggest physical interactions
among these proteins. This conclusion was confirmed by experiments using
the yeast two-hybrid assay, which demonstrated the following pairwise
interactions: Rad4 with Rad23, Rad4 with Rad7, and Rad7 with Rad16.
Additionally, interaction between the Rad7 and Rad16 proteins was
demonstrated in vitro. Our results show that Rad7, Rad16, and Rad23 are
required for transcription-independent NER in vitro. This process may
involve a unique protein complex which is distinct from the repairosome and
which contains at least the Rad4, Rad7, and Rad16 proteins.
Copyright © 1997, American Society for Microbiology
The RAD7, RAD16, and RAD23 genes of Saccharomyces cerevisiae: requirement for transcription-independent nucleotide excision repair in vitro and interactions between the gene products
Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235, USA.
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