DNA and RNA as new binding targets of green tea catechins

被引:121
作者
Kuzuhara, Takashi [1 ]
Sei, Yoshihisa
Yamaguchi, Kentaro
Suganuma, Masami
Fujiki, Hirota
机构
[1] Univ Tokushima, Fac Pharmaceut Sci, Biochem Lab, Yamashiro, Tokushima 7708514, Japan
[2] Tokushima Bunri Univ, Fac Pharmaceut Sci, Analyt Chem Lab, Sanuki, Kagawa 7692193, Japan
关键词
D O I
10.1074/jbc.M601196200
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 significance of catechins, the main constituent of green tea, is being increasingly recognized with regard to cancer prevention. Catechins have been studied for interactions with various proteins, but the mechanisms of the various catechins are not yet elucidated. Based on our previous observation that nucleic acids extracted from catechin-treated cells are colored, we studied whether catechins directly interact with nucleic acids using surface plasmon resonance assay(Biacore) and cold spray ionization-mass spectrometry. These two methods clearly showed that (-)-epigallocatechin gallate (EGCG) binds to both DNA and RNA molecules: the Biacore assay indicated that four catechins bound to DNA oligomers, and cold spray ionization-mass spectrometry analysis showed one to three EGCG molecules bound to single strand 18 mers of DNA and RNA. Moreover, one or two molecules of EGCG bound to double-stranded (AG-CT) oligomers of various nucleotide lengths. These results suggest that multiple binding sites of EGCG are present in DNA and RNA oligomers. Double-stranded DNA(dsDNA) oligomers were detected only as EGCG-bound forms at high temperature, whereas at low temperature both the free and bound forms were detected, suggesting that EGCG protects dsDNA oligomers from dsDNA melting to single-stranded DNA. Because both galloyl and catechol groups of EGCG are essential for DNA binding, both groups seem to hold strands of DNA via their branching structure. These findings reveal for the first time the link between catechins and polynucleotides and will intensify our understanding of the effects of catechins on DNA in terms of cancer prevention.
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页码:17446 / 17456
页数:11
相关论文
共 31 条
[1]   Green tea polyphenol and curcumin inversely regulate human involucrin promoter activity via opposing effects on CCAAT/enhancer-binding protein function [J].
Balasubramanian, S ;
Eckert, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :24007-24014
[2]   Green tea constituent (-)-epigallocatechin-3-gallate inhibits topoisomerase I activity in human colon carcinoma cells [J].
Berger, SJ ;
Gupta, S ;
Belfi, CA ;
Gosky, DM ;
Mukhtar, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 288 (01) :101-105
[3]   Induction of poly (ADP-ribosyl)ation and DNA damage in human peripheral lymphocytes after treatment with (-)-epigallocatechin-gallate [J].
Bertram, B ;
Bollow, U ;
Rajaee-Behbahani, N ;
Bürkle, A ;
Schmezer, P .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2003, 534 (1-2) :77-84
[4]  
Fang MZ, 2003, CANCER RES, V63, P7563
[5]   Two stages of cancer prevention with green tea [J].
Fujiki, H .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1999, 125 (11) :589-597
[6]   Green tea: Health benefits as cancer preventive for humans [J].
Fujiki, H .
CHEMICAL RECORD, 2005, 5 (03) :119-132
[7]   Translational research on TNF-α as an endogenous tumor promoter and green tea as cancer preventive in humans [J].
Fujiki, H ;
Suganuma, M .
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART C-ENVIRONMENTAL CARCINOGENESIS & ECOTOXICOLOGY REVIEWS, 2005, 23 (01) :3-30
[8]   Green tea and cancer prevention [J].
Fujiki, H ;
Suganuma, M .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2002, 78 (09) :263-270
[9]   Green tea: cancer preventive beverage and/or drug [J].
Fujiki, H ;
Suganuma, M ;
Imai, K ;
Nakachi, K .
CANCER LETTERS, 2002, 188 (1-2) :9-13
[10]  
Fujimoto N, 2002, INT J ONCOL, V20, P1233