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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收藏
页码:9246 / 9255
页数:10
相关论文
共 60 条
  • [1] STRUCTURES FOR POLYNUCLEOTIDE COMPLEXES POLY(DA).POLY(DT) AND POLY(DT).POLY(DA).POLY(DT)
    ARNOTT, S
    SELSING, E
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1974, 88 (02) : 509 - +
  • [2] STRUCTURES FOR POLYINOSINIC ACID AND POLYGUANYLIC ACID
    ARNOTT, S
    CHANDRASEKARAN, R
    MARTTILA, CM
    [J]. BIOCHEMICAL JOURNAL, 1974, 141 (02) : 537 - +
  • [3] ARNOTT S, 1976, NUCLEIC ACIDS RES, V3, P2458
  • [4] THE HUMAN C-MYC-ONCOGENE - STRUCTURAL CONSEQUENCES OF TRANSLOCATION INTO THE IGH LOCUS IN BURKITT-LYMPHOMA
    BATTEY, J
    MOULDING, C
    TAUB, R
    MURPHY, W
    STEWART, T
    POTTER, H
    LENOIR, G
    LEDER, P
    [J]. CELL, 1983, 34 (03) : 779 - 787
  • [5] 2ND STRUCTURAL MOTIF FOR RECOGNITION OF DNA BY OLIGONUCLEOTIDE-DIRECTED TRIPLE-HELIX FORMATION
    BEAL, PA
    DERVAN, PB
    [J]. SCIENCE, 1991, 251 (4999) : 1360 - 1363
  • [6] DNA-STRUCTURE EQUILIBRIA IN THE HUMAN C-MYC GENE
    BOLES, TC
    HOGAN, ME
    [J]. BIOCHEMISTRY, 1987, 26 (02) : 367 - 376
  • [7] POLYNUCLEOTIDES .16. FORMATION OF THE TRIPLE-STRANDED POLYNUCLEOTIDE HELIX, POLY(A-A-U)
    BROITMAN, SL
    IM, DD
    FRESCO, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) : 5120 - 5124
  • [8] SITE-SPECIFIC OLIGONUCLEOTIDE BINDING REPRESSES TRANSCRIPTION OF THE HUMAN C-MYC GENE INVITRO
    COONEY, M
    CZERNUSZEWICZ, G
    POSTEL, EH
    FLINT, SJ
    HOGAN, ME
    [J]. SCIENCE, 1988, 241 (4864) : 456 - 459
  • [9] RIBONUCLEOPROTEIN AND PROTEIN FACTORS BIND TO AN H-DNA-FORMING C-MYC DNA ELEMENT - POSSIBLE REGULATORS OF THE C-MYC GENE
    DAVIS, TL
    FIRULLI, AB
    KINNIBURGH, AJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) : 9682 - 9686
  • [10] NMR-STUDIES OF DNA (R+)N.(Y-)N.(Y+)N TRIPLE HELICES IN SOLUTION - IMINO AND AMINO PROTON MARKERS OF T.A.T AND C.G.C+ BASE-TRIPLE FORMATION
    DELOSSANTOS, C
    ROSEN, M
    PATEL, D
    [J]. BIOCHEMISTRY, 1989, 28 (18) : 7282 - 7289