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J. Biol. Chem., Vol. 266, Issue 33, 22472-22478, 11, 1991
ZG Wang, XH Wu and EC Friedberg
Nucleotide excision repair is a complex biochemical process that corrects
DNA damage caused by a broad spectrum of physical and chemical agents. We
examined the effect of the assembly of ultraviolet- irradiated plasmid DNA
into nucleosomes on nucleotide excision repair supported by human cell
extracts. Repair synthesis in unassembled UV- irradiated plasmid DNA was
readily detected in extracts from repair- proficient human cells. In
contrast, repair synthesis was markedly suppressed in UV-irradiated DNA
assembled into nucleosomes (minichromosomes). This suppression occurred at
a step(s) which precedes repair synthesis during nucleotide excision
repair. Human cell extracts were unable to effectively assemble plasmid DNA
into nucleosomes under repair synthesis conditions. The addition of
purified histones to the extracts restored their capacity for nucleosome
assembly and simultaneously led to the suppression of repair synthesis. We
propose that the preferential repair of actively transcribed genes relative
to transcriptionally silent genes may reflect altered nucleosome
conformation during transcription.
Nucleotide excision repair of DNA by human cell extracts is suppressed in reconstituted nucleosomes
Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235.
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