The crystal structures of psoralen cross-linked DNAs: Drug-dependent formation of Holliday junctions

被引:43
作者
Eichman, BF
Mooers, BHM
Alberti, M
Hearst, JE
Ho, PS
机构
[1] Oregon State Univ, Dept Biochem & Biophys, Corvallis, OR 97331 USA
[2] Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
DNA-binding drug; DNA structure; Holliday junction; psoralen; recombination;
D O I
10.1006/jmbi.2001.4567
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
The single-crystal structures are presented for two DNA sequences with the thymine bases covalently cross-linked across the complementary strands by 4 ' -hydroxymethyl-4,5 ' ,8-trimethylpsoralen (HMT). The HMT-adduct of d(CCGCTAGCGG) forms a psoralen-induced Holliday junction, showing for the first time the effect of this important class of chemotheraputics on the structure of the recombination intermediate. In contrast, HMT-d(CCGGTACCGG) forms a sequence-dependent junction. Ln both structures, the DNA duplex is highly distorted at the thymine base linked to the six-member pyrone ring of the drug. The psoralen cross-link defines the intramolecular interactions of the drug-induced junction, while the sequence-dependent structure is nearly identical to the native Holliday junction of d(CCGGTACCGG) alone. The two structures contrast the effects of drug- and sequence-dependent interactions on the structure of a Holliday junction, suggesting a role for psoralen in the mechanism to initiate repair of psoralen-lesions in mammalian DNA. (C) 2001 Academic Press.
引用
收藏
页码:15 / 26
页数:12
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