A critical survey of the structure-function of the antisense oligo/RNA heteroduplex as substrate for RNase H

被引:101
作者
Zamaratski, E [1 ]
Pradeepkumar, PI [1 ]
Chattopadhyaya, J [1 ]
机构
[1] Univ Uppsala, Ctr Biomed, Dept Bioorgan Chem, S-75123 Uppsala, Sweden
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2001年 / 48卷 / 03期
关键词
structure; DNA/RNA hybrid; AONs; RNase H;
D O I
10.1016/S0165-022X(01)00149-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this review is to draw a correlation between the structure of the DNA/RNA hybrid and its properties as a substrate for the RNase H, as well as to point the crucial structural requirements for the modified AONs to preserve their RNase H potency. The review is divided into the following parts: (1) mechanistic considerations, (2) target RNA folding-AON folding-RNase H assistance in AON/RNA hybrid formation, (3) carbohydrate modifications, (4) backbone modifications, (5) base modifications, (6) conjugated AONs, (7) importance of the tethered chromophore in AON for the AON/RNA hybrid interactions with the RNase H. The structural changes in the AON/RNA hybrid duplexes brought by different modifications of the sugar, backbone or base in the antisense strand, and the effect of these changes on the RNase H recognition of the modified substrates have been addressed. Only those AON modifications and the corresponding AON/RNA hybrids, which have been structurally characterized by spectroscopic means and functionally analyzed by their ability to elicit RNase H potency in comparison with the native counterpart have been presented here. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:189 / 208
页数:20
相关论文
共 98 条
  • [91] Cyclohexene nucleic acids (CeNA): Serum stable oligonucleotides that activate RNase H and increase duplex stability with complementary RNA
    Wang, J
    Verbeure, B
    Luyten, I
    Lescrinier, E
    Froeyen, M
    Hendrix, C
    Rosemeyer, H
    Seela, F
    Van Aerschot, A
    Herdewijn, P
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (36) : 8595 - 8602
  • [92] Synthesis of 3′-C- and 4′-C-branched oligodeoxynucleotides and the development of locked nucleic acid (LNA)
    Wengel, J
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (04) : 301 - 310
  • [93] RIBONUCLEASES-H OF RETROVIRAL AND CELLULAR-ORIGIN
    WINTERSBERGER, U
    [J]. PHARMACOLOGY & THERAPEUTICS, 1990, 48 (02) : 259 - 280
  • [94] Molecular cloning and expression of cDNA for human RNase H
    Wu, HJ
    Lima, WF
    Crooke, ST
    [J]. ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1998, 8 (01): : 53 - 61
  • [95] WU HJ, 1999, J BIOL CHEM, V272, P6146
  • [96] STRUCTURE OF RIBONUCLEASE-H PHASED AT 2-A RESOLUTION BY MAD ANALYSIS OF THE SELENOMETHIONYL PROTEIN
    YANG, W
    HENDRICKSON, WA
    CROUCH, RJ
    SATOW, Y
    [J]. SCIENCE, 1990, 249 (4975) : 1398 - 1405
  • [97] Stereo-enriched phosphorothioate oligodeoxgnucleotides: Synthesis, biophysical and biological properties
    Yu, D
    Kandimalla, ER
    Roskey, A
    Zhao, QY
    Chen, LH
    Chen, JD
    Agrawal, S
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2000, 8 (01) : 275 - 284
  • [98] The 3′-modified antisense oligos promote faster hydrolysis of the target RNA by RNase H than the natural counterpart
    Zamaratski, E
    Ossipov, D
    Pradeepkumar, PI
    Amirkhanov, N
    Chattopadhyaya, J
    [J]. TETRAHEDRON, 2001, 57 (03) : 593 - 606