DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall.

Abstract:

:DNA repair was measured in the dihydrofolate reductase gene in Chinese hamster ovary cells, amplified for the gene, by quantitating pyrimidine dimers with a specific UV-endonuclease. More than two thirds of the dimers had been removed from a 14.1 kb restriction fragment of the gene by 26 hr after irradiation (20 J/m2), while little removal was detected in fragments upstream of the gene and only 15% were removed from the genome overall. This suggests that damage processing can vary according to function or activity of affected sequences, which has general implications for correlations of DNA repair with survival and mutagenesis. Perhaps preferential repair of vital sequences facilitates UV-resistance of these cells despite low overall repair levels.

journal_name

Cell

journal_title

Cell

authors

Bohr VA,Smith CA,Okumoto DS,Hanawalt PC

doi

10.1016/0092-8674(85)90150-3

subject

Has Abstract

pub_date

1985-02-01 00:00:00

pages

359-69

issue

2

eissn

0092-8674

issn

1097-4172

pii

0092-8674(85)90150-3

journal_volume

40

pub_type

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