Fully modified 2′ MOE oligonucleotides redirect polyadenylation

被引:88
作者
Vickers, TA [1 ]
Wyatt, JR [1 ]
Burckin, T [1 ]
Bennett, CF [1 ]
Freier, SM [1 ]
机构
[1] ISIS Pharmaceut, Dept Mol & Struct Biol, Carlsbad, CA 92008 USA
关键词
D O I
10.1093/nar/29.6.1293
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
Many genes have been described and characterized that have alternative polyadenylation signals at the 3'-end of their pre-mRNAs, Many of these same messages also contain destabilization motifs responsible for vapid degradation of the mRNA. Polyadenylation site selection can thus determine the stability of an mRNA, Fully modified 2'-O-methoxy ethyl/phosphorothioate oligonucleotides that hybridize to the 3'-most polyadenylation site or signal of E-selectin were able to inhibit polyadenylation at this site and redirect it to one of two upstream cryptic sites. The shorter transcripts produced after antisense treatment have fewer destabilization sequences, increased mRNA stability and altered protein expression. This study demonstrates that antisense oligonucleotides can be successfully employed to redirect polyadenylation. This is the first demonstration of the use of oligonucleotides to increase, rather than decrease, abundance of a message.
引用
收藏
页码:1293 / 1299
页数:7
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