Engineered riboregulators enable post-transcriptional control of gene expression

被引:415
作者
Isaacs, FJ
Dwyer, DJ
Ding, CM
Pervouchine, DD
Cantor, CR
Collins, JJ
机构
[1] Boston Univ, Ctr Biodynam, Boston, MA 02215 USA
[2] Boston Univ, Ctr Adv Biotechnol, Boston, MA 02215 USA
[3] Boston Univ, Bioinformat Program, Boston, MA 02215 USA
[4] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[5] Boston Univ, Dept Biol, Boston, MA 02215 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nbt986
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recent studies have demonstrated the important enzymatic, structural and regulatory roles of RNA in the cell. Here we present a post-transcriptional regulation system in Escherichia coli that uses RNA to both silence and activate gene expression. We inserted a complementary cis sequence directly upstream of the ribosome binding site in a target gene. Upon transcription, this cis-repressive sequence causes a stem-loop structure to form at the 5'-untranslated region of the mRNA. The stem-loop structure interferes with ribosome binding, silencing gene expression. A small noncoding RNA that is expressed in trans targets the cis-repressed RNA with high specificity, causing an alteration in the stem-loop structure that activates expression. Such engineered riboregulators may lend insight into mechanistic actions of endogenous RNA-based processes and could serve as scalable components of biological networks, able to function with any promoter or gene to directly control gene expression.
引用
收藏
页码:841 / 847
页数:7
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