INDUCTION OF CYCLOBUTANE PYRIMIDINE DIMER PHOTOLYASE IN CULTURED FISHCELLS BY FLUORESCENT LIGHT AND OXYGEN STRESS
Citation
H. Mitani et A. Shima, INDUCTION OF CYCLOBUTANE PYRIMIDINE DIMER PHOTOLYASE IN CULTURED FISHCELLS BY FLUORESCENT LIGHT AND OXYGEN STRESS, Photochemistry and photobiology, 61(4), 1995, pp. 373-377
Categorie Soggetti
Biophysics,Biology
SICI code
0031-8655(1995)61:4<373:IOCPDP>2.0.ZU;2-C
Abstract
The expression of a gene for photolyase in RBCF-1 cells, a line of cul
tured goldfish cells, is known to be enhanced by fluorescent light. We
have now found that H2O2 is another strong inducer of cyclobutane pyr
imidine dimer photolyase. Northern blot analysis suggested that regula
tion by H2O2 occurs at the transcriptional level and the time course o
f induction of photolyase by H2O2 was similar to that by fluorescent l
ight. Treatment with fluorescent light in the presence of riboflavin,
which is known as an endogenous photosensitizer, also enhanced the ind
uction of photolyase. These results suggest the involvement of oxygen
stress in the induction of photolyase by fluorescent light. A cell clo
ne with high-level expression of the goldfish gene for photolyase was
obtained by transfection with plasmids that expressed the goldfish pho
tolyase in OL32 cells derived from another fish, the medaka (Oryzias l
atipes). The induction of the medaka gene for photolyase was not affec
ted by the high-level expression of the goldfish gene for this enzyme.