Physicochemical and biochemical properties of 2′,5′-linked RNA and 2′,5′-RNA:3′,5′-RNA "hybrid" duplexes

被引:59
作者
Wasner, M
Arion, D
Borkow, G
Noronha, A
Uddin, AH
Parniak, MA
Damha, MJ
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 2K6, Canada
[2] McGill Univ, Fac Med, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, McGill AIDS Ctr, Montreal, PQ H3T 1E2, Canada
关键词
D O I
10.1021/bi980160b
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 recent publications, oligonucleotides joined by 2',5'-linkages were found to bind to complementary single-stranded RNA but to bind weakly, or not at all, to single-stranded DNA [e.g., P. A. Giannaris and M. J. Damha (1993) Nucleic Acids Res. 21, 4742-4749]. In this work, the biochemical and physicochemical properties of 2',5'-linked oligoribonucleotides containing mixed sequences of the four nucleobases (A, G, C, and U) were evaluated. CD spectra of RNA:2',5'-RNA duplexes were compared with the spectra of DNA:DNA, RNA:RNA, and DNA:RNA duplexes of the same base sequence. The CD results indicated that the RNA:2',5'-RNA duplex structure more closely resembles the structure of the RNA:DNA hybrid, being more A-form than B-form in character. The melting temperature (T-m) values of the backbone-modified duplexes were compared with the T-m values of the unmodified duplexes. The order of thermal stability was RNA:RNA > DNA:DNA approximate to RNA:DNA approximate to DNA:RNA > RNA:2',5'-RNA > 2',5'-RNA:2',5'-RNA much greater than DNA:2',5'-RNA (undetected). RNA:2',5'-RNA duplexes are not substrates of the enzyme RNase H (Escherichia coli, or HIV-1 reverse transcriptase), but they can inhibit the RNase H-mediated cleavage of a natural DNA:RNA substrate. Structural models that are consistent with the selective association properties of 2',5'-linked oligonucleotides are discussed.
引用
收藏
页码:7478 / 7486
页数:9
相关论文
共 54 条
[1]  
ALBERTS B, 1989, MOL BIOL CELL, P304
[2]   (2'-5')-OLIGO-3'-DEOXYNUCLEOTIDES - SELECTIVE BINDING TO SINGLE-STRANDED RNA BUT NOT DNA [J].
ALUL, R ;
HOKE, GD .
ANTISENSE RESEARCH AND DEVELOPMENT, 1995, 5 (01) :3-11
[3]  
ARTS EJ, 1994, J BIOL CHEM, V269, P14672
[4]   The role of backbone oxygen atoms in the organization of nucleic acid tertiary structure: zippers, networks, clamps, and C-H center dot center dot center dot O hydrogen bonds [J].
Berger, I ;
Egli, M .
CHEMISTRY-A EUROPEAN JOURNAL, 1997, 3 (09) :1400-1404
[5]   2',5'-linked oligo-3'-deoxyribonucleoside phosphorothioate chimeras: thermal stability and antisense inhibition of gene expression [J].
Bhan, P ;
Bhan, A ;
Hong, MK ;
Hartwell, JG ;
Saunders, JM ;
Hoke, GD .
NUCLEIC ACIDS RESEARCH, 1997, 25 (16) :3310-3317
[6]   Inhibitory potency of R-region specific antisense oligonucleotides against in vitro DNA polymerization and template-switching reactions catalysed by HIV-1 reverse transcriptase [J].
Borkow, G ;
Arion, D ;
Noronha, A ;
Scartozzi, M ;
Damha, MJ ;
Parniak, MA .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (11) :1285-1295
[7]   CONFORMATIONAL STABILITY OF DINUCLEOTIDES IN SOLUTION [J].
BRAHMS, J ;
MAURIZOT, JC ;
MICHELSON, AM .
JOURNAL OF MOLECULAR BIOLOGY, 1967, 25 (03) :481-+
[8]   CD, absorption and thermodynamic analysis of repeating dinucleotide DNA, RNA and hybrid duplexes [d/r(AC)](12)center dot[d/r(GT/U)](12) and the influence of phosphorothioate substitution [J].
Clark, CL ;
Cecil, PK ;
Singh, D ;
Gray, DM .
NUCLEIC ACIDS RESEARCH, 1997, 25 (20) :4098-4105
[9]  
CROOKE ST, 1993, ANTISENSE RES APPL, P579
[10]  
Damha M J, 1993, Methods Mol Biol, V20, P81