Engineering high-speed allosteric hammerhead ribozymes

被引:42
|
作者
Link, Kristian H.
Gu, Lixia
Ames, Tyler D.
Yen, Laising
Mulligan, Richard C.
Breaker, Ronald R. [1 ]
机构
[1] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[3] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[4] Harvard Univ, Sch Med, Dept Genet, Harvard Inst Human Genet, Boston, MA 02115 USA
关键词
aptamer; riboswitch; RNA folding; RNA switch; self-cleavage; theophylline;
D O I
10.1515/BC.2007.105
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
Full-length hammerhead ribozymes were subjected to in vitro selection to identify variants that are allosterically regulated by theophylline in the presence of a physiologically relevant concentration of Mg2+. The population of allosteric ribozymes resulting from 15 rounds of in vitro selection yielded variants with observed rate constants (k(obs)) as high as 8 min(-1) in the presence of theophylline and maximal k(obs) increases of up to 285-fold compared to rate constants measured in the absence of effector. The selected ribozymes have kinetic characteristics that are predicted to be sufficient for cellular gene control applications, but do not exhibit any activity in reporter gene assays. The inability of the engineered RNAs to control gene expression suggests that the in vitro and in vivo folding pathways of the RNAs are different. These results provide several key pieces of information that will aid in future efforts to engineer allosteric ribozymes for gene control applications.
引用
收藏
页码:779 / 786
页数:8
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