BINDING OF TRIPLE HELIX FORMING OLIGONUCLEOTIDES TO SITES IN GENE PROMOTERS

被引:270
作者
DURLAND, RH
KESSLER, DJ
GUNNELL, S
DUVIC, M
PETTITT, BM
HOGAN, ME
机构
[1] BAYLOR COLL MED, CTR BIOTECHNOL, THE WOODLANDS, TX 77381 USA
[2] UNIV TEXAS, DEPT CHEM, HOUSTON, TX 77204 USA
[3] UNIV TEXAS, SCH MED, DEPT DERMATOL & INTERNAL MED, HOUSTON, TX 77030 USA
关键词
D O I
10.1021/bi00102a017
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
A class of triplex-forming oligodeoxyribonucleotides (TFOs) is described that can bind to naturally occurring sites in duplex DNA at physiological pH in the presence of magnesium. The data are consistent with a structure in which the TFO binds in the major groove of double-stranded DNA to form a three-stranded complex that is superficially similar to previously described triplexes. The distinguishing features of this class of triplex are that TFO binding apparently involves the formation of hydrogen-bonded G.GC and T.AT triplets and the TFO is bound antiparallel with respect to the more purine-rich strand of the underlying duplex. Triplex formation is described for targets in the promoter regions of three different genes: the human c-myc and epidermal growth factor receptor genes and the mouse insulin receptor gene. All three sites are relatively GC rich and have a high percentage of purine residues on one strand. DNase I footprinting shows that individual TFOs bind selectively to their target sites at pH 7.4-7.8 in the presence of millimolar concentrations of magnesium. Electrophoretic analysis of triplex formation indicates that specific TFOs bind to their target sites with apparent dissociation constants in the 10(-7)-10(-9) M range. Strand orientation of the bound TFOs was confirmed by attaching eosin or an iron-chelating group to one end of the TFO and monitoring the pattern of damage to the bound duplex DNA. Possible hydrogen-bonding patterns and triplex structures are discussed.
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页码:9246 / 9255
页数:10
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