High potency silencing by single-stranded boranophosphate siRNA

被引:82
作者
Hall, Allison H. S.
Wan, Jing
Spesock, April
Sergueeva, Zinaida
Shaw, Barbara Ramsay
Alexander, Kenneth A.
机构
[1] Duke Univ, Ctr Med, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[2] Duke Univ, Dept Chem, Durham, NC 27708 USA
[3] Univ Chicago, Sect Pediat Infect Dis, Dept Pediat, Chicago, IL 60637 USA
关键词
D O I
10.1093/nar/gkl339
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 RNA interference (RNAi), double-stranded short interfering RNA (ds-siRNA) inhibits expression from complementary mRNAs. Recently, it was demonstrated that short, single-stranded antisense RNA (ss-siRNA) can also induce RNAi. While ss-siRNA may offer several advantages in both clinical and research applications, its overall poor activity compared with ds-siRNA has prevented its widespread use. In contrast to the poor gene silencing activity of native ss-siRNA, we found that the silencing activity of boranophosphate-modified ss-siRNA is comparable with that of unmodified ds-siRNA. Boranophosphate ss-siRNA has excellent maximum silencing activity and is highly effective at low concentrations. The silencing activity of boranophosphate ss-siRNA is also durable, with significant silencing up to 1 week after transfection. Thus, we have demonstrated that boranophosphate-modified ss-siRNA can silence gene expression as well as native ds-siRNA, suggesting that boranophosphate-modified ss-siRNAs should be investigated as a potential new class of therapeutic agents.
引用
收藏
页码:2773 / 2781
页数:9
相关论文
共 50 条
[1]   High potency silencing by boranophosphate sirna: Synthesis, properties, and silencing activities [J].
Wan, J ;
Seraueeva, Z ;
Hall, A ;
Alexander, K ;
Shaw, BR .
ANTIVIRAL RESEARCH, 2006, 70 (01) :A39-A40
[2]   Single-stranded siRNA therapeutics [J].
Pamela Feliciano .
Nature Genetics, 2012, 44 (10) :1079-1079
[3]   Single-stranded siRNAs for in vivo gene silencing [J].
Markus Elsner .
Nature Biotechnology, 2012, 30 :1063-1063
[4]   Single-stranded siRNAs for in vivo gene silencing [J].
Elsner, Markus .
NATURE BIOTECHNOLOGY, 2012, 30 (11) :1063-1063
[5]   Modulation of Splicing by Single-Stranded Silencing RNAs [J].
Liu, Jing ;
Hu, Jiaxin ;
Hicks, Jessica A. ;
Prakash, Thazha P. ;
Corey, David R. .
NUCLEIC ACID THERAPEUTICS, 2015, 25 (03) :113-120
[6]   Single-Stranded Phosphorothioated Regions Enhance Cellular Uptake of Cholesterol-Conjugated siRNA but Not Silencing Efficacy [J].
Ly, Socheata ;
Echeverria, Dimas ;
Sousa, Jacquelyn ;
Khvorova, Anastasia .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2020, 21 :991-1005
[7]   Single-Stranded Silencing RNAs: Hit Rate and Chemical Modification [J].
Pendergraff, Hannah M. ;
Debacker, Alexandre J. ;
Watts, Jonathan K. .
NUCLEIC ACID THERAPEUTICS, 2016, 26 (04) :216-222
[8]   In situ analysis of single-stranded and duplex siRNA integrity in living cells [J].
Raemdonck, Koen ;
Remaut, Katrien ;
Lucas, Bart ;
Sanders, Niek N. ;
Demeester, Jo ;
De Smedt, Stefaan C. .
BIOCHEMISTRY, 2006, 45 (35) :10614-10623
[9]   Collision-induced Dissociation of Intact Duplex and Single-Stranded siRNA Anions [J].
Huang, Teng-yi ;
Liu, Jian ;
Liang, Xiaorong ;
Hodges, Brittany D. M. ;
McLuckey, Scott A. .
ANALYTICAL CHEMISTRY, 2008, 80 (22) :8501-8508
[10]   Transcriptional Silencing of Arabidopsis Endogenes by Single-Stranded RNAs Targeting the Promoter Region [J].
Deng, Shulin ;
Dai, Hongzheng ;
Arenas, Catalina ;
Wang, Huan ;
Niu, Qi-Wen ;
Chua, Nam-Hai .
PLANT AND CELL PHYSIOLOGY, 2014, 55 (04) :823-833