ELSAMICIN-A CAN CONVERT THE Z-FORM OF POLY[D(G-C)] AND POLY[D(G-M(5)C)] BACK TO B-FORM DNA

被引:17
作者
JIMENEZGARCIA, E [1 ]
PORTUGAL, J [1 ]
机构
[1] UNIV BARCELONA, FAC QUIM, DEPT BIOQUIM & FISIOL, BARCELONA 7, SPAIN
关键词
D O I
10.1021/bi00161a051
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
The interaction of poly[(G-C)] and poly[d(G-m5C)] with the antitumor antibiotic elsamicin A, which binds to alternating guanine + cytosine tracts in DNA, has been studied under the B and Z conformations. Both the rate and the extent of the B-to-Z transition are diminished by the antibiotic, as inferred by spectroscopic methods under ionic conditions that otherwise favor the left-handed conformation of the polynucleotides. Moreover, elsamicin converts the Z-form DNA back to the B-form. The circular dichroism data indicate that elsamicin binds to poly[d(G-C)] and poly[d(G-m5C)] to form a right-handed bound elsamicin region(s). The transition can be followed by changes of the molar ellipticity at 250 nm, thus providing a convenient wavelength to monitor the Z-to-B conformational change of the polymers as elsamicin is added. The elsamicin A effect might be explained by a model in which the antibiotic binds preferently to a B-form DNA, playing a role as an allosteric effector on the equilibrium between the B and Z conformations, thus favoring the right-handed one.
引用
收藏
页码:11641 / 11646
页数:6
相关论文
共 37 条
[1]   ISOLATION OF Z-DNA BINDING-PROTEINS FROM SV40 MINICHROMOSOMES - EVIDENCE FOR BINDING TO THE VIRAL CONTROL REGION [J].
AZORIN, F ;
RICH, A .
CELL, 1985, 41 (02) :365-374
[2]   SELECTIVE DISPLACEMENT OF NUCLEAR PROTEINS BY ANTITUMOR DRUGS HAVING AFFINITY FOR NUCLEIC-ACIDS [J].
BARTKOWIAK, J ;
KAPUSCINSKI, J ;
MELAMED, MR ;
DARZYNKIEWICZ, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :5151-5154
[3]   EFFECTS OF METHYLATION ON A SYNTHETIC POLYNUCLEOTIDE - THE B-Z TRANSITION IN POLY(DG-M5DC).POLY(DG-M5DC) [J].
BEHE, M ;
FELSENFELD, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (03) :1619-1623
[4]  
BERNASCONI CF, 1976, RELAXATION KINETICS, P148
[5]   INVIVO ASSESSMENT OF THE Z-DNA-FORMING POTENTIAL OF D(CA.GT)N AND D(CG.GC)N SEQUENCES CLONED INTO SV40 MINICHROMOSOMES [J].
CASASNOVAS, JM ;
ELLISON, MJ ;
RODRIGUEZCAMPOS, A ;
MARTINEZBALBAS, A ;
AZORIN, F .
JOURNAL OF MOLECULAR BIOLOGY, 1989, 208 (04) :537-549
[6]  
CHAIRES JB, 1986, J BIOL CHEM, V261, P8899
[7]  
CHAIRES JB, 1990, JERUS SYM Q, V23, P123
[8]   DAUNOMYCIN INHIBITS THE B-]Z TRANSITION IN POLY D(G-C) [J].
CHAIRES, JB .
NUCLEIC ACIDS RESEARCH, 1983, 11 (23) :8485-8494
[9]   LONG-RANGE ALLOSTERIC EFFECTS ON THE B TO Z EQUILIBRIUM BY DAUNOMYCIN [J].
CHAIRES, JB .
BIOCHEMISTRY, 1985, 24 (25) :7479-7486
[10]   INTERACTION OF NETROPSIN AND DISTAMYCIN WITH DEOXYRIBONUCLEIC-ACID - ELECTRIC DICHROISM STUDY [J].
DATTAGUPTA, N ;
HOGAN, M ;
CROTHERS, DM .
BIOCHEMISTRY, 1980, 19 (26) :5998-6005