Frayed wires: A thermally stable form of DNA with two distinct structural domains

被引:83
作者
Protozanova, E [1 ]
Macgregor, RB [1 ]
机构
[1] UNIV TORONTO, FAC PHARM, TORONTO, ON M5S 2S2, CANADA
关键词
D O I
10.1021/bi960412d
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
In aqueous solutions containing mono- and divalent cations, the oligodeoxyribonucleotide d(A(15)G(15)) readily self-assembles into high-molecular weight species that resolve as discrete bands on native and denaturing electrophoresis gels. The complexes consist of an integer number of strands of d(A(15)G(15)), the number of strands range from one (the monomer) to greater than nine. The complexes form within a few minutes even at low concentrations (2 mu M strands) of d(A(15)G(15)), The relative concentration of species is determined by the solvent conditions, The complexes are resistant to standard denaturation conditions, 50% formamide heated to 95 degrees C for 2 min followed by electrophoresis in 7 RI urea at 55 degrees C. In the proposed modal for the oligomers and polymers of d(A(15)G(15)), several molecules of d(A(15)G(15)) interact via a stem of tetraplex structure formed by the guanine residues, The 15 guanine residues in the stem account for its high stability. The 5' end adenines form single-stranded arms that are displaced from the guanine-containing stem. The arms can participate in the formation of Watson-Crick base pairs with dT(10) and other partially complementary oligodeoxyribonucleotides such as d(CT15). Engagement of the arms in interactions with other strands does not affect the distribution of the species between different conformations. On the other hand, the addition of the Fully complementary oligodeoxyribonucleotide d(C15T15) to the polymer leads to the disappearance of the high-molecular weight complexes and results in the formation of a canonical Watson-Crick base-paired duplex, The type and concentration of the cation present in solution determine which conformation d(A(15)G(15)) will adopt. Divalent cations at millimolar concentrations lead to the formation of the polymer, while the presence of the monovalent cations stabilizes lower-molecular weight complexes consisting of two to Six strands of d(A(15)G(15)).
引用
收藏
页码:16638 / 16645
页数:8
相关论文
共 22 条
[1]   SOLUTION STRUCTURE OF A PARALLEL-STRANDED TETRAPLEX FORMED BY D(TG(4)T) IN THE PRESENCE OF SODIUM-IONS BY NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY [J].
ABOULELA, F ;
MURCHIE, AIH ;
NORMAN, DG ;
LILLEY, DMJ .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 243 (03) :458-471
[2]   STRUCTURE AND FUNCTION OF TELOMERES [J].
BLACKBURN, EH .
NATURE, 1991, 350 (6319) :569-573
[3]   ABSORPTION AND OPTICAL ROTATORY DISPERSION OF 7 TRINUCLEOSIDE DIPHOSPHATES [J].
CANTOR, CR ;
TINOCO, I .
JOURNAL OF MOLECULAR BIOLOGY, 1965, 13 (01) :65-&
[4]   OLIGONUCLEOTIDE INTERACTIONS .3. CIRCULAR DICHROISM STUDIES OF CONFORMATION OF DEOXYOLIGONUCLEOTIDES [J].
CANTOR, CR ;
WARSHAW, MM ;
SHAPIRO, H .
BIOPOLYMERS, 1970, 9 (09) :1059-&
[5]   ACID-FACILITATED SUPRAMOLECULAR ASSEMBLY OF G-QUADRUPLEXES IN D(CGG)(4) [J].
CHEN, FM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (39) :23090-23096
[6]   SELF-ASSEMBLY OF DNA OLIGOMERS INTO HIGH-MOLECULAR-WEIGHT SPECIES [J].
DAI, TY ;
MAROTTA, SP ;
SHEARDY, RD .
BIOCHEMISTRY, 1995, 34 (11) :3655-3662
[7]   THE BETA-SUBUNIT OF OXYTRICHA TELOMERE-BINDING PROTEIN PROMOTES G-QUARTET FORMATION BY TELOMERIC DNA [J].
FANG, GW ;
CECH, TR .
CELL, 1993, 74 (05) :875-885
[8]   DIRECT OBSERVATION OF A DNA QUADRUPLEX BY ELECTROSPRAY IONIZATION MASS-SPECTROMETRY [J].
GOODLETT, DR ;
CAMP, DG ;
HARDIN, CC ;
CORREGAN, M ;
SMITH, RD .
BIOLOGICAL MASS SPECTROMETRY, 1993, 22 (03) :181-183
[9]   STRUCTURE OF A PARALLEL-STRANDED TETRAMER OF THE OXYTRICHA TELOMERIC DNA-SEQUENCE DT4G4 [J].
GUPTA, G ;
GARCIA, AE ;
GUO, Q ;
LU, M ;
KALLENBACH, NR .
BIOCHEMISTRY, 1993, 32 (28) :7098-7103
[10]   CATION-DEPENDENT TRANSITION BETWEEN THE QUADRUPLEX AND WATSON-CRICK HAIRPIN FORMS OF D(CGCG3GCG) [J].
HARDIN, CC ;
WATSON, T ;
CORREGAN, M ;
BAILEY, C .
BIOCHEMISTRY, 1992, 31 (03) :833-841