A specificity comparison of four antisense types: Morpholino, 2'-O-methyl RNA, DNA, and phosphorothioate DNA

被引:111
作者
Stein, D
Foster, E
Huang, SB
Weller, D
Summerton, J
机构
[1] ANTIVIRALS Inc., Corvallis
[2] ANTIVIRALS Inc., Corvallis, OR 97333
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 1997年 / 7卷 / 03期
关键词
D O I
10.1089/oli.1.1997.7.151
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
Cell-free translation studies were carried out to compare the efficacy and specificity of four antisense structural types: DNA, phosphorothioate DNA (S-DNA), 2'-O-methyl RNA, and Morpholino oligos, a novel antisense structural type, In these studies, translational inhibition was assessed for two 20-mers of each structural type, where one 20-mer was complementary to its target sequence in rabbit alpha-globin mRNA and the other 20-mer contained three mispairs to that same target sequence, It is shown that at low concentration of antisense oligomer (50 nM) all four types provide high specificity, but the Morpholino oligos and 2'-O-methyl RNA afford better efficacy, At high oligomer concentration (3.5 mu M), all four types provide high efficacy, but the Morpholino oligos and 2'-O-methyl RNA provide substantially better specificity than the DNA and S-DNA.
引用
收藏
页码:151 / 157
页数:7
相关论文
共 14 条
[1]   INHIBITION OF RABBIT GLOBIN MESSENGER-RNA TRANSLATION BY SEQUENCE-SPECIFIC OLIGODEOXYRIBONUCLEOTIDES [J].
BLAKE, KR ;
MURAKAMI, A ;
MILLER, PS .
BIOCHEMISTRY, 1985, 24 (22) :6132-6138
[2]   COMPARATIVE INHIBITION OF RABBIT GLOBIN MESSENGER-RNA TRANSLATION BY MODIFIED ANTISENSE OLIGODEOXYNUCLEOTIDES [J].
CAZENAVE, C ;
STEIN, CA ;
LOREAU, N ;
THUONG, NT ;
NECKERS, LM ;
SUBASINGHE, C ;
HELENE, C ;
COHEN, JS ;
TOULME, JJ .
NUCLEIC ACIDS RESEARCH, 1989, 17 (11) :4255-4273
[3]  
Crouch R. J., 1982, NUCLEASES, P211
[4]   Resistance of morpholino phosphorodiamidate oligomers to enzymatic degradation [J].
Hudziak, RM ;
Barofsky, E ;
Barofsky, DF ;
Weller, DL ;
Huang, SB ;
Weller, DD .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1996, 6 (04) :267-272
[5]   RNASE H-MEDIATED INHIBITION OF TRANSLATION BY ANTISENSE OLIGODEOXYRIBO-NUCLEOTIDES - USE OF BACKBONE MODIFICATION TO IMPROVE SPECIFICITY [J].
LARROUY, B ;
BLONSKI, C ;
BOIZIAU, C ;
STUER, M ;
MOREAU, S ;
SHIRE, D ;
TOULME, JJ .
GENE, 1992, 121 (02) :189-194
[6]   RNASE-H IS RESPONSIBLE FOR THE NONSPECIFIC INHIBITION OF IN-VITRO TRANSLATION BY 2'-O-ALKYL CHIMERIC OLIGONUCLEOTIDES - HIGH-AFFINITY OR SELECTIVITY, A DILEMMA TO DESIGN ANTISENSE OLIGOMERS [J].
LARROUY, B ;
BOIZIAU, C ;
SPROAT, B ;
TOULME, JJ .
NUCLEIC ACIDS RESEARCH, 1995, 23 (17) :3434-3440
[7]  
MEZL V, 1981, ANAL BIOCHEM, V177, P452
[8]  
PAVLAKIS GN, 1980, CELL, V19, P91, DOI 10.1016/0092-8674(80)90391-8
[9]  
RAYNER B, 1989, OLIGODEOXYNUCLEOTIDE, P119
[10]   INHIBITION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV-1) REPLICATION BY SYNTHETIC OLIGO-RNA DERIVATIVES [J].
SHIBAHARA, S ;
MUKAI, S ;
MORISAWA, H ;
NAKASHIMA, H ;
KOBAYASHI, S ;
YAMAMOTO, N .
NUCLEIC ACIDS RESEARCH, 1989, 17 (01) :239-252