Inter-strand photoproducts are produced in high yield within A-DNA exposed to UVC radiation

被引:80
作者
Douki, T [1 ]
Laporte, G [1 ]
Cadet, J [1 ]
机构
[1] CEA Grenoble, Dept Rech Fondamentale Mat Condensee, DSM,Serv Chim Inorgan & Biol,FRE 2600, Lab Les Acides Nucl, F-38054 Grenoble 9, France
关键词
D O I
10.1093/nar/gkg408
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Far-UV irradiation of DNA leads to the dimerization of pyrimidine bases, resulting in the formation of cyclobutane type dimers and ( 6 - 4) photoproducts. In the dry state, an additional thymine dimeric photolesion, the spore photoproduct, is also generated. While most photoproducts are expected to be produced between adjacent pyrimidines, little attention has been paid to lesions involving bases located on different DNA strands. Using HPLC - mass spectrometry analysis of enzymatically digested DNA, we observed that, in the dry state, inter-strand dimeric photoproducts represented 30% of the total yield of dimeric thymine lesions. The major inter-strand damage was found to be the spore photoproduct. Formation of inter-strand lesions in significant yield could be obtained in solution upon modification of the DNA conformation as the result of the addition of large amounts of ethanol. In both cases, DNA is in the A-form, which is characterized by a high compaction, likely to favor inter-strand photoreactions. Since the latter DNA conformation is also predominant in bacterial spores, the formation and repair of dimeric photoproducts involving thymine bases located on different DNA strands may thus be relevant in terms of deleterious effects of UV radiation to the latter microorganisms.
引用
收藏
页码:3134 / 3142
页数:9
相关论文
共 63 条
[1]   FORMATION OF A THYMINE PHOTOPRODUCT IN TRANSFORMING DNA BY NEAR UV IRRADIATION [J].
CABRERAJUAREZ, E ;
SETLOW, JK .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 475 (02) :315-322
[2]   RAPID QUANTITATION OF ULTRAVIOLET-INDUCED THYMINE-CONTAINING DIMERS IN HUMAN CELL-DNA BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
CADET, J ;
GENTNER, NE ;
ROZGA, B ;
PATERSON, MC .
JOURNAL OF CHROMATOGRAPHY, 1983, 280 (01) :99-108
[3]  
Cadet J., 1990, Bioorganic Photochemistry: Photochemistry and the Nucleic Acids, V1, P1
[4]   Direct H atom abstraction from spore photoproduct C-6 initiates DNA repair in the reaction catalyzed by spore photoproduct lyase: Evidence for a reversibly generated adenosyl radical intermediate [J].
Cheek, J ;
Broderick, JB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (12) :2860-2861
[5]   A-B CONFORMATIONAL CHANGE IN SODIUM SALT OF DNA [J].
COOPER, PJ ;
HAMILTON, LD .
JOURNAL OF MOLECULAR BIOLOGY, 1966, 16 (02) :562-&
[6]   T4 DNA-POLYMERASE (3'-5') EXONUCLEASE, AN ENZYME FOR THE DETECTION AND QUANTITATION OF STABLE DNA LESIONS - THE ULTRAVIOLET-LIGHT EXAMPLE [J].
DOETSCH, PW ;
CHAN, GL ;
HASELTINE, WA .
NUCLEIC ACIDS RESEARCH, 1985, 13 (09) :3285-3304
[7]   THYMINE PHOTOPRODUCTS BUT NOT THYMINE DIMERS FOUND IN ULTRAVIOLET-IRRADIATED BACTERIAL SPORES [J].
DONNELLAN, JE ;
SETLOW, RB .
SCIENCE, 1965, 149 (3681) :308-+
[8]   Formation of the main UV-induced thymine dimeric lesions within isolated and cellular DNA as measured by high performance liquid chromatography-tandem mass spectrometry [J].
Douki, T ;
Court, M ;
Sauvaigo, S ;
Odin, F ;
Cadet, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (16) :11678-11685
[9]   Formation of the spore photoproduct and other dimeric lesions between adjacent pyrimidines in UVC-irradiated dry DNA [J].
Douki, T ;
Cadet, J .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2003, 2 (04) :433-436
[10]   Formation of 2′-deoxyuridine hydrates upon exposure of nucleosides to gamma radiation and UVC-irradiation of isolated and cellular DNA [J].
Douki, T ;
Vadesne-Bauer, G ;
Cadet, J .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2002, 1 (08) :565-569