Base pair opening in three DNA-unwinding elements

被引:17
作者
Coman, D
Russu, IM [1 ]
机构
[1] Wesleyan Univ, Dept Chem, Hall Atwater Labs 203, Middletown, CT 06459 USA
[2] Wesleyan Univ, Mol Biophys Program, Hall Atwater Labs 203, Middletown, CT 06459 USA
关键词
D O I
10.1074/jbc.M502773200
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
DNA-unwinding elements are specific base sequences that are located in the origin of DNA replication where they provide the start point for strand separation and unwinding of the DNA double helix. In the present work we have obtained the first characterization of the opening of individual base pairs in DNA-unwinding elements. The three DNA molecules investigated reproduce the 13-mer DNA-unwinding elements present in the Escherichia coli chromosome. The base sequences of the three 13-mers are conserved in the origins of replication of enteric bacterial chromosomes. The exchange of imino protons with solvent protons was measured for each DNA as a function of the concentration of exchange catalyst using nuclear magnetic resonance spectroscopy. The exchange rates provided the rates and the equilibrium constants for opening of individual base pairs in each DNA at 20 degrees C. The results reveal that the kinetics and energetics of the opening reactions for AT/TA base pairs are different in the three DNA-unwinding elements due to long range effects of the base sequence. These differences encompass the AT/TA base pairs that are conserved in various bacterial genomes. Furthermore, a qualitative correlation is observed between the kinetics and energetics of opening of AT/TA base pairs and the location of the corresponding DNA-unwinding element in the origin of DNA replication.
引用
收藏
页码:20216 / 20221
页数:6
相关论文
共 29 条
[1]   SITES OF PREDICTED STRESS-INDUCED DNA DUPLEX DESTABILIZATION OCCUR PREFERENTIALLY AT REGULATORY LOCI [J].
BENHAM, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2999-3003
[2]   MELTING OF A SELF-COMPLEMENTARY DNA MINICIRCLE - COMPARISON OF OPTICAL MELTING THEORY WITH EXCHANGE BROADENING OF THE NUCLEAR MAGNETIC-RESONANCE SPECTRUM [J].
BENIGHT, AS ;
SCHURR, JM ;
FLYNN, PF ;
REID, BR ;
WEMMER, DE .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 200 (02) :377-399
[3]  
Boulikas T, 1996, J CELL BIOCHEM, V60, P297, DOI 10.1002/(SICI)1097-4644(19960301)60:3<297::AID-JCB2>3.0.CO
[4]  
2-R
[5]   DUPLEX OPENING BY DNAA PROTEIN AT NOVEL SEQUENCES IN INITIATION OF REPLICATION AT THE ORIGIN OF THE ESCHERICHIA-COLI CHROMOSOME [J].
BRAMHILL, D ;
KORNBERG, A .
CELL, 1988, 52 (05) :743-755
[6]   PREDICTING DNA DUPLEX STABILITY FROM THE BASE SEQUENCE [J].
BRESLAUER, KJ ;
FRANK, R ;
BLOCKER, H ;
MARKY, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :3746-3750
[7]   OLIGONUCLEOTIDE INTERACTIONS .3. CIRCULAR DICHROISM STUDIES OF CONFORMATION OF DEOXYOLIGONUCLEOTIDES [J].
CANTOR, CR ;
WARSHAW, MM ;
SHAPIRO, H .
BIOPOLYMERS, 1970, 9 (09) :1059-&
[8]   Site-resolved stabilization of a DNA triple helix by magnesium ions [J].
Coman, D ;
Russu, IM .
NUCLEIC ACIDS RESEARCH, 2004, 32 (03) :878-883
[9]   Site-resolved energetics in DNA triple helices containing G•TA and T•CG triads [J].
Coman, D ;
Russu, IM .
BIOCHEMISTRY, 2002, 41 (13) :4407-4414
[10]   The DnaC helicase loader is a dual ATP/ADP switch protein [J].
Davey, MJ ;
Fang, LH ;
McInerney, P ;
Georgescu, RE ;
O'Donnell, M .
EMBO JOURNAL, 2002, 21 (12) :3148-3159