» Articles » PMID: 12888501

The Activity of SiRNA in Mammalian Cells is Related to Structural Target Accessibility: a Comparison with Antisense Oligonucleotides

Overview
Specialty Biochemistry
Date 2003 Jul 31
PMID 12888501
Citations 103
Authors
Affiliations
Soon will be listed here.
Abstract

The biological activity of siRNA seems to be influenced by local characteristics of the target RNA, including local RNA folding. Here, we investigated quantitatively the relationship between local target accessibility and the extent of inhibition of the target gene by siRNA. Target accessibility was assessed by a computational approach that had been shown earlier to be consistent with experimental probing of target RNA. Two sites of ICAM-1 mRNA predicted to serve as accessible motifs and one site predicted to adopt an inaccessible structure were chosen to test siRNA constructs for suppression of ICAM-1 gene expression in ECV304 cells. The local target-dependent effectiveness of siRNA was compared with antisense oligonucleotides (asON). The concentration dependency of siRNA-mediated suppression indicates a >1000-fold difference between active siRNAs (IC50 approximately 0.2-0.5 nM) versus an inactive siRNA (IC50 > or = 1 microM) which is consistent with the activity pattern of asON when relating target suppression to predicted local target accessibility. The extremely high activity of the siRNA si2B (IC50 = 0.24 nM) indicates that not all siRNAs shown to be active at the usual concentrations of >10-100 nM belong to this highly active species. The observations described here suggest an option to assess target accessibility for siRNA and, thus, support the design of active siRNA constructs. This approach can be automated, work at high throughput and is open to include additional parameters relevant to the biological activity of siRNA.

Citing Articles

The roles of long non-coding RNAs in ovarian cancer: from functions to therapeutic implications.

Hu Z, Yuan L, Yang X, Yi C, Lu J Front Oncol. 2024; 14:1332528.

PMID: 38725621 PMC: 11079149. DOI: 10.3389/fonc.2024.1332528.


Small interfering RNA (siRNA)-based therapeutic applications against viruses: principles, potential, and challenges.

Kang H, Ga Y, Kim S, Cho Y, Kim J, Kim C J Biomed Sci. 2023; 30(1):88.

PMID: 37845731 PMC: 10577957. DOI: 10.1186/s12929-023-00981-9.


RNA Secondary Structure Analysis Using RNAstructure.

Ali S, Mittal A, Mathews D Curr Protoc. 2023; 3(7):e846.

PMID: 37487054 PMC: 11267465. DOI: 10.1002/cpz1.846.


Antisense Oligonucleotide Therapy for the Nervous System: From Bench to Bedside with Emphasis on Pediatric Neurology.

Amanat M, Nemeth C, Smith Fine A, Leung D, Fatemi A Pharmaceutics. 2022; 14(11).

PMID: 36365206 PMC: 9695718. DOI: 10.3390/pharmaceutics14112389.


Antisense Oligonucleotides and Small Interfering RNA for the Treatment of Dyslipidemias.

Gareri C, Polimeni A, Giordano S, Tamme L, Curcio A, Indolfi C J Clin Med. 2022; 11(13).

PMID: 35807171 PMC: 9267663. DOI: 10.3390/jcm11133884.


References
1.
Patzel V, Steidl U, Kronenwett R, Haas R, Sczakiel G . A theoretical approach to select effective antisense oligodeoxyribonucleotides at high statistical probability. Nucleic Acids Res. 1999; 27(22):4328-34. PMC: 148713. DOI: 10.1093/nar/27.22.4328. View

2.
Vickers T, Koo S, Bennett C, Crooke S, Dean N, Baker B . Efficient reduction of target RNAs by small interfering RNA and RNase H-dependent antisense agents. A comparative analysis. J Biol Chem. 2002; 278(9):7108-18. DOI: 10.1074/jbc.M210326200. View

3.
Sczakiel G . Theoretical and experimental approaches to design effective antisense oligonucleotides. Front Biosci. 2000; 5:D194-201. DOI: 10.2741/sczakiel. View

4.
Scherr M, Rossi J, Sczakiel G, Patzel V . RNA accessibility prediction: a theoretical approach is consistent with experimental studies in cell extracts. Nucleic Acids Res. 2000; 28(13):2455-61. PMC: 102709. DOI: 10.1093/nar/28.13.2455. View

5.
Bramlage B, Luzi E, Eckstein F . HIV-1 LTR as a target for synthetic ribozyme-mediated inhibition of gene expression: site selection and inhibition in cell culture. Nucleic Acids Res. 2000; 28(21):4059-67. PMC: 113160. DOI: 10.1093/nar/28.21.4059. View