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Transcriptional Silencing by Single-Stranded RNAs Targeting a Noncoding RNA That Overlaps a Gene Promoter
被引:18
|作者:
Matsui, Masayuki
[1
,2
]
Prakash, Thazha P.
[3
]
Corey, David R.
[1
,2
]
机构:
[1] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
[3] ISIS Pharmaceut, Carlsbad, CA 92010 USA
基金:
美国国家卫生研究院;
关键词:
SIRNAS;
ARGONAUTE2;
CLEAVAGE;
D O I:
10.1021/cb300490j
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:
RNAi using single-strand RNA would provide new options for therapeutic development and for investigating critical questions of mechanism. Using chemically modified single-strands, we test the hypothesis that single-stranded RNAs can engage the RNAi pathway and silence gene transcription. We find that a chemically modified single-stranded silencing RNA (ss-siRNA) designed to be complementary to a long noncoding RNA (IncRNA) requires argonaute protein, functions through the RNAi pathway, and inhibits gene transcription. These data expand the use of single-stranded RNA to cell nuclei.
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页码:122 / 126
页数:5
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