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PMID: 8506394 Published · ppublish English Comparative Study Journal Article

Differential expression of pyrimidine dimer-binding proteins in normal and UV light-treated vertebrate cells.

Photochemistry and photobiology ·Vol. 57 ·No. 4 ·1993-04-00 ·Pages 655-62

McLenigan M, Levine AS, Protić M

Abstract

The expression of UV damage-specific DNA-binding proteins was examined in various phylogenetically distant species with differing DNA repair phenotypes. Two distinct constitutive DNA-binding activities, one specific for cyclobutane pyrimidine dimers and the other for non-cyclobutane dimer photoproducts, were detected. The expression of these binding activities was found to be variable throughout the animal kingdom: cold-blooded vertebrates show a constitutive cyclobutane dimer-binding activity exclusively, and primates reveal only non-cyclobutane binding activity. In contrast, birds and marsupials appear to express both types of binding activities. The kinetics of expression (rather than the constitutive presence) of these UV damage-specific DNA-binding activities after UV treatment correlate with the cell's capacity for DNA repair. In addition, cyclobutane pyrimidine dimer-binding activities could be detected only in cells with established photoreactivating activity.

MeSH Terms
Animals Base Sequence Cell Line DNA Damage DNA Repair/genetics DNA-Binding Proteins/genetics,isolation & purification,metabolism Humans Molecular Sequence Data Oligodeoxyribonucleotides Phenotype Pyrimidine Dimers/metabolism Species Specificity Ultraviolet Rays Vertebrates
Chemicals
DNA-Binding Proteins Oligodeoxyribonucleotides Pyrimidine Dimers
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
McLenigan M
Section on Viruses and Cellular Biology, National Institute of Child Health and Human Development, Bethesda, MD 20892.
Levine A S
Protić M
Article Info
Journal
Photochemistry and photobiology
Abbr.
Photochem Photobiol
ISSN
0031-8655
Published
1993-04-00
Pages
655-62
Language
English
Region
United States
NLM ID
0376425
Subset
IM
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