Effect of cytosine methylation on DNA-DNA recognition at CpG steps

被引:33
作者
MayerJung, C [1 ]
Moras, D [1 ]
Timsit, Y [1 ]
机构
[1] ULP,INSERM,INST GENET & BIOL MOL & CELLULAIRE,LAB BIOL STRUCT,CNRS,F-67404 ILLKIRCH GRAFFENS,FRANCE
关键词
oligonucleotide; crystal structure; cytosine methylation; DNA condensation; C-H-O bonds;
D O I
10.1006/jmbi.1997.1137
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
Although DNA methylation is a fundamental mechanism for repressing genetic activity, the influence of methyl groups on DNA conformation is found to be small. In this study, the role of cytosine methylation is analysed in the context of DNA condensation by examining its influence on DNA-DNA recognition processes. Previously CpG sites were found to act as sequence determinants for the close and specific self-fit of B-DNA helices into cross-overs. In the present study, the crystal structure of the B-DNA dodecamer d(ACCGCCGGCGCC) methylated at its central CpG sequence shows that the methyl groups do nest interfere with DNA self-fitting. In contrast the two methyl groups form a clamp, which traps the incoming phosphate in the groove-backbone interaction. This geometry allows the formation of two new C-H ... O hydrogen bonds between the methyl groups and. the anionic oxygen atoms of the phosphate, which may further stabilize the interaction. This finding relates cytosine methylation to the formation of higher-order DNA structures and could provide new insights for understanding the mode of action of DNA methylation in genetic inactivation. (C) 1997 Academic Press Limited.
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页码:328 / 335
页数:8
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