PNA oligomers as tools for specific modulation of gene expression
被引:65
作者:
Pooga, M
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机构:Estonian Bioctr, EE-51010 Tartu, Estonia
Pooga, M
Land, T
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机构:Estonian Bioctr, EE-51010 Tartu, Estonia
Land, T
Bartfai, T
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机构:Estonian Bioctr, EE-51010 Tartu, Estonia
Bartfai, T
Langel, Ü
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机构:Estonian Bioctr, EE-51010 Tartu, Estonia
Langel, Ü
机构:
[1] Estonian Bioctr, EE-51010 Tartu, Estonia
[2] Stockholm Univ, Arrhenius Lab, Dept Neurochem & Neurotoxicol, S-10691 Stockholm, Sweden
[3] Scripps Res Inst, Dept Neuropharmacol, Harold L Dorris Neurol Res Ctr, La Jolla, CA 92037 USA
来源:
BIOMOLECULAR ENGINEERING
|
2001年
/
17卷
/
06期
关键词:
antigene;
antisense;
PNA;
PNA delivery;
D O I:
10.1016/S1389-0344(01)00075-2
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Small synthetic molecules that can specifically inhibit translation and/or transcription have shown great promise as potential antisense/antigene drugs. Peptide nucleic acid (PNA), an oligonucleotide mimic, has a non-charged achiral polyamide backbone to which the nucleobases are attached. PNA oligomers are extremely stable in biological fluids and they specifically hybridise to DNA or RNA in a complementary manner, forming very strong heteroduplexes. Some of the mRNAs have yet undetermined and possibly long half-lives, successful down regulation of gene expression by antisense oligonucleotides (ON) requires that the antisense agent is long lived. PNA fulfils this requirement better than phosphodiester or phsphorothioate ONs. PNA can inhibit transcription and translation of respective genes by tight binding to DNA or mRNA. First in vitro experiments to specifically down regulate protein expression by PNA have been followed by successful antisense and antigene application of PNA oligomers in vivo. This review discusses the principles of the in vitro and in vivo use of PNA oligonucleotides. (C) 2001 Elsevier Science B.V. All rights reserved.