CHEMISTRY OF THERMAL-DEGRADATION OF ABASIC SITES IN DNA - MECHANISTIC INVESTIGATION ON THERMAL DNA STRAND CLEAVAGE OF ALKYLATED DNA

被引:71
作者
SUGIYAMA, H [1 ]
FUJIWARA, T [1 ]
URA, A [1 ]
TASHIRO, T [1 ]
YAMAMOTO, K [1 ]
KAWANISHI, S [1 ]
SAITO, I [1 ]
机构
[1] KYOTO UNIV,FAC MED,DEPT PUBL HLTH,KYOTO 606,JAPAN
关键词
D O I
10.1021/tx00041a013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The chemistry of thermal degradation of aldehydic abasic sites in DNA was investigated. Sequencing gel analysis of duocarmycin A-treated 5'-P-32-end-labeled DNA fragment indicated that upon heating at neutral pH alkylated DNA was cleaved to provide fragments possessing a modified sugar moiety which is readily decomposed to 3'-phosphate terminus by piperidine treatment. To identify the structure of modified sugar product and to investigate the mechanism of thermal cleavage, thermal degradation of various oligonucleotides containing abasic sites was investigated in detail. It was found that heating the DNA containing an abasic site induces beta-elimination to provide 3'-termini possessing a trans-alpha,beta-unsaturated aldose residue together with 5'-phosphate termini. Upon prolonged heating at pH 7.0, the trans-alpha,beta-unsaturated aldose terminus is isomerized to a cis isomer or is further degraded to its hydrated products and a 3'-phosphate terminus via delta-elimination. This type of thermal degradation also occurs in the abasic site-containing calf thymus DNA. Investigation of the stereochemical course of the thermal beta-elimination reaction using a 2-pro-R-D-containing abasic site has demonstrated that the reaction proceeds via a syn-elimination process as observed for the enzymatic reaction of UV endonuclease V and endonuclease III.
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页码:673 / 683
页数:11
相关论文
共 52 条
[1]   NOVEL INTERSTRAND CROSS-LINKS INDUCED BY THE ANTITUMOR ANTIBIOTIC CARZINOPHILIN AZINOMYCIN-B [J].
ARMSTRONG, RW ;
SALVATI, ME ;
NGUYEN, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (08) :3144-3145
[2]   SEQUENCE-SPECIFIC CLEAVAGE OF DNA BY N-BROMOACETYLDISTAMYCIN - PRODUCT AND KINETIC ANALYSES [J].
BAKER, BF ;
DERVAN, PB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (07) :2700-2712
[3]  
Boger D L, 1994, Bioorg Med Chem, V2, P115, DOI 10.1016/S0968-0896(00)82007-6
[4]  
Boger D. L., 1991, CHEMTRACTS ORG CHEM, V4, P329
[5]   REVERSIBILITY OF THE DUOCARMYCIN-A AND SA DNA ALKYLATION REACTION [J].
BOGER, DL ;
YUN, WY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (21) :9872-9873
[6]   SYNTHESIS AND PRELIMINARY EVALUATION OF AGENTS INCORPORATING THE PHARMACOPHORE OF THE DUOCARMYCIN PYRINDAMYCIN ALKYLATION SUBUNIT - IDENTIFICATION OF THE CC-1065 DUOCARMYCIN COMMON PHARMACOPHORE [J].
BOGER, DL ;
ISHIZAKI, T ;
ZARRINMAYEH, H ;
KITOS, PA ;
SUNTORNWAT, O .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (15) :4499-4502
[7]   ISOLATION AND CHARACTERIZATION OF THE DUOCARMYCIN ADENINE DNA ADDUCT [J].
BOGER, DL ;
ISHIZAKI, T ;
ZARRINMAYEH, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (17) :6645-6649
[8]   (+)- AND ENT-(-)-DUOCARMYCIN SA AND (+)- AND ENT-(-)-N-BOC-DSA DNA ALKYLATION PROPERTIES - ALKYLATION SITE MODELS THAT ACCOMMODATE THE OFFSET AT-RICH ADENINE N3 ALKYLATION SELECTIVITY OF THE ENANTIOMERIC AGENTS [J].
BOGER, DL ;
JOHNSON, DS ;
YUN, WY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (05) :1635-1656
[9]   DUOCARMYCIN PYRINDAMYCIN DNA ALKYLATION PROPERTIES AND IDENTIFICATION, SYNTHESIS, AND EVALUATION OF AGENTS INCORPORATING THE PHARMACOPHORE OF THE DUOCARMYCIN PYRINDAMYCIN ALKYLATION SUBUNIT - IDENTIFICATION OF THE CC-1065-DUOCARMYCIN COMMON PHARMACOPHORE [J].
BOGER, DL ;
ISHIZAKI, T ;
ZARRINMAYEH, H ;
MUNK, SA ;
KITOS, PA ;
SUNTORNWAT, O .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (24) :8961-8971
[10]   DNA ALKYLATION PROPERTIES OF ENHANCED FUNCTIONAL ANALOGS OF CC-1065 INCORPORATING THE 1,2,9,9A-TETRAHYDROCYCLOPROPA[1,2-C]BENZ[1,2-E]INDOL-4-ONE (CBI) ALKYLATION SUBUNIT [J].
BOGER, DL ;
MUNK, SA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (14) :5487-5496