Identification and quantification of a guanine-thymine intrastrand cross-link lesion induced by Cu(II)/H2O2/ascorbate

被引:89
作者
Hong, Haizheng
Cao, Huachuan
Wang, Yuesong [1 ]
Wang, Yinsheng
机构
[1] Univ Calif Riverside, Environm Toxicol Grad Program, Riverside, CA 92521 USA
[2] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
关键词
D O I
10.1021/tx060025x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Reactive oxygen species (ROS) can be induced by both endogenous and exogenous processes, and they can damage biological molecules including nucleic acids. It was shown that X- or gamma-ray irradiation of aqueous solutions of DNA, during which (OH)-O-center dot is one of the major ROS, can lead to the formation of intrastrand cross-link lesions where the neighboring nucleobases in the same DNA strand are covalently bonded. Previous P-32-postlabeling studies suggested that the intrastrand cross- link lesions may arise from Fenton reaction, which also induces the formation of (OH)-O-center dot; the structures of the proposed intrastrand cross- link lesions, however, have not been determined. Here, we showed for the first time that the treatment of calf thymus DNA with Cu(II)/H2O2/ascorbate could lead to the formation of an intrastrand cross-link lesion, i.e., G boolean AND T, where the C8 of guanine is covalently bonded to the neighboring 3'- thymine through its methyl carbon. LC-MS/ MS quantification results showed dose-responsive formation of G boolean AND T. In addition, the yield of the intrastrand cross- link was approximately 3 orders of magnitude lower than those of commonly observed single-base lesions, that is, 8-oxo-7,8-dihydro-2'- deoxyguanosine, 5-( hydroxymethyl)2'- deoxyuridine, and 5-formyl-2'-deoxyuridine. The induction of intrastrand cross- link lesion in calf thymus DNA by Fenton reagents in vitro suggests that this type of lesion might be formed endogenously in mammalian cells.
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页码:614 / 621
页数:8
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共 63 条
[41]   Distinct mechanisms of site-specific DNA damage induced by endogenous reductants in the presence of iron(III) and copper(II) [J].
Oikawa, S ;
Kawanishi, S .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1998, 1399 (01) :19-30
[42]   INTERACTION OF COPPER(I) WITH NUCLEIC-ACIDS [J].
PRUTZ, WA ;
BUTLER, J ;
LAND, EJ .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1990, 58 (02) :215-234
[43]   INTENSIFICATION AND DEPLETION OF SPECIFIC BULKY RENAL DNA-ADDUCTS (I-COMPOUNDS) FOLLOWING EXPOSURE OF MALE F344 RATS TO THE RENAL CARCINOGEN FERRIC NITRILOTRIACETATE (FE-NTA) [J].
RANDERATH, E ;
WATSON, WP ;
ZHOU, GD ;
CHANG, J ;
RANDERATH, K .
MUTATION RESEARCH-GENETIC TOXICOLOGY, 1995, 341 (04) :265-279
[44]   BULKY ADDUCTS DETECTED BY P-32 POSTLABELING IN DNA MODIFIED BY OXIDATIVE DAMAGE INVITRO - COMPARISON WITH RAT LUNG I-COMPOUNDS [J].
RANDERATH, K ;
YANG, PF ;
DANNA, TF ;
REDDY, R ;
WATSON, WP ;
RANDERATH, E .
MUTATION RESEARCH, 1991, 250 (1-2) :135-144
[45]   A 32P-Postlabeling assay for the oxidative DNA lesion 8,5′-cyclo-2′-deoxyadenosine in mammalian tissues -: Evidence that four type II I-compounds are dinucleotides containing the lesion in the 3′ nucleotide [J].
Randerath, K ;
Zhou, GD ;
Somers, RL ;
Robbins, JH ;
Brooks, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (38) :36051-36057
[46]   AGE-RELATED AND TISSUE-RELATED DNA MODIFICATIONS IN UNTREATED RATS - DETECTION BY P-32 POSTLABELING ASSAY AND POSSIBLE SIGNIFICANCE FOR SPONTANEOUS TUMOR-INDUCTION AND AGING [J].
RANDERATH, K ;
REDDY, MV ;
DISHER, RM .
CARCINOGENESIS, 1986, 7 (09) :1615-1617
[47]   Structural origins of bulky oxidative DNA adducts (Type II I-compounds) as deduced by oxidation of oligonucleotides of known sequence [J].
Randerath, K ;
Randerath, E ;
Smith, CV ;
Chang, J .
CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (01) :247-254
[48]   Bulky endogenous DNA modifications (I-compounds) - possible structural origins and functional implications [J].
Randerath, K ;
Randerath, E ;
Zhou, GD ;
Li, DH .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 424 (1-2) :183-194
[49]   Singlet oxygen induces oxidation of cellular DNA [J].
Ravanat, JL ;
Di Mascio, P ;
Martinez, GR ;
Medeiros, MHG ;
Cadet, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (51) :40601-40604
[50]   TANDEM DOUBLE CC-]TT MUTATIONS ARE PRODUCED BY REACTIVE OXYGEN SPECIES [J].
REID, TM ;
LOEB, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) :3904-3907