NMR evidence for base dynamics at all TpA steps in DNA

被引:18
作者
McAteer, K [1 ]
Kennedy, MA [1 ]
机构
[1] Pacific NW Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
关键词
D O I
10.1080/07391102.2000.10506588
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
NMR evidence is presented indicating that the exceptional conformational dynamics found at TpA steps in DNA is general to all immediate sequence contexts. One easily tractable NMR parameter that is sensitive to TpA base dynamics is the resonance linewidth of the TpA adenine H2 proton. This resonance experiences a temperature-dependent broadening due to conformational dynamics. Unusual dynamics at TpA steps were originally observed in the sequence context (T)pTpTpApAp(A). We have since shown that the evidence for TpA dynamics persists when either the thymine preceding the TpA step or the adenine following the TpA step is preserved [McAteer et al., Nucleic Acids Res. 23, 3962-3966 (1995)]. Here, in order establish whether or not exceptional TpA dynamics occurs in all DNA sequence contexts, we investigated a series of DNA sequences of the form GCN(a)TAN(b)N(b)TAN(a)GC, where N=A,T,C,G. In this family of sequences, all 16 possible immediate sequence context environments of the form N(a)TAN(b) were examined using 10 DNA sequences. Our NMR results show that the TpA adenine H2 resonance contains a temperature dependent excess linewidth indicative of dynamics in all 16 sequence context environments. By studying a complete set of sequence contexts, it was possible to recognize trends relating resonance parameters and sequence environment. For example, the magnitude of the maximum linewidth is largely determined by the identity of the nucleotide following the TpA step and the magnitude of the linewidth maximum is moderately correlated (r=0.56) with the temperature of the linewidth maximum. The physical basis for these correlations is discussed.
引用
收藏
页码:1001 / 1009
页数:9
相关论文
共 23 条
[1]   PROTON NMR-STUDIES OF [N-MECYS3,N-MECYS7]TANDEM BINDING TO DNA OLIGONUCLEOTIDES - SEQUENCE-SPECIFIC BINDING AT THE TPA SITE [J].
ADDESS, KJ ;
GILBERT, DE ;
OLSEN, RK ;
FEIGON, J .
BIOCHEMISTRY, 1992, 31 (02) :339-350
[2]   STRUCTURAL DETAILS OF AN ADENINE TRACT THAT DOES NOT CAUSE DNA TO BEND [J].
BURKHOFF, AM ;
TULLIUS, TD .
NATURE, 1988, 331 (6155) :455-457
[3]  
CROTHERS DM, 1990, J BIOL CHEM, V265, P7093
[4]   INTERMOLECULAR NUCLEAR SHIELDING VALUES FOR PROTONS OF PURINES AND FLAVINS [J].
GIESSNERPRETTRE, C ;
PULLMAN, B .
JOURNAL OF THEORETICAL BIOLOGY, 1970, 27 (01) :87-+
[5]   SEQUENCE-DIRECTED CURVATURE OF DNA [J].
HAGERMAN, PJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :755-781
[6]   Differences between DNA base pair stacking energies are conserved over a wide range of ionic conditions [J].
Johnson, T ;
Zhu, J ;
Wartell, RM .
BIOCHEMISTRY, 1998, 37 (35) :12343-12350
[7]   MOBILITY AT THE TPA CLEAVAGE SITE IN THE T3A3-CONTAINING AHAIII AND PMEI RESTRICTION SEQUENCES [J].
KENNEDY, MA ;
NUUTERO, ST ;
DAVIS, JT ;
DROBNY, GP ;
REID, BR .
BIOCHEMISTRY, 1993, 32 (31) :8022-8035
[8]   CO-CRYSTAL STRUCTURE OF TBP RECOGNIZING THE MINOR-GROOVE OF A TATA ELEMENT [J].
KIM, JL ;
NIKOLOV, DB ;
BURLEY, SK .
NATURE, 1993, 365 (6446) :520-527
[9]   EFFECTS OF CHAIN-LENGTH ON SECONDARY STRUCTURE OF OLIGOADENYLATES [J].
KROON, PA ;
KREISHMAN, GP ;
NELSON, JH ;
CHAN, SI .
BIOPOLYMERS, 1974, 13 (12) :2571-2592
[10]  
LANE AN, 1993, EUR BIOPHYS J BIOPHY, V21, P425, DOI 10.1007/BF00185870