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RNA-directed off/on switch of RNase H activity using boronic ester formation
Organic & Biomolecular Chemistry ( IF 3.2 ) Pub Date : 2017-09-12 00:00:00 , DOI: 10.1039/c7ob02145c
Maëva Reverte 1, 2, 3, 4, 5 , Ivan Barvik 6, 7, 8, 9, 10 , Jean-Jacques Vasseur 1, 2, 3, 4, 5 , Michael Smietana 1, 2, 3, 4, 5
Affiliation  

RNase H is a non-specific endonuclease which degrades selectively the RNA strand in DNA/RNA duplexes. We demonstrate in the present study that 5′-boronic acid modified oligonucleotides hybridized to a RNA target sequence converts RNase H to an inactivated enzyme complex. The dynamic formation of a boronate ester upon addition of a diol moiety disrupts the enzyme-inhibitor complex and reactivates RNase H. Moreover, we show that reactivation of RNase H function can also be engineered through short RNA trimers inputs that fashion RNase H from a non-specific DNA-guided enzyme into an informational and programmable RNA-guided one. Examples of programmable RNA recognition and cleavage illustrate the potential of this new stimuli-responsive system.

中文翻译:

使用硼酸酯形成的RNA定向的RNase H活性的开关

RNase H是一种非特异性核酸内切酶,可选择性降解DNA / RNA双链体中的RNA链。我们在本研究中证明,与RNA靶序列杂交的5'-硼酸修饰的寡核苷酸可将RNase H转化为灭活的酶复合物。加入二醇部分后,硼酸酯的动态形成会破坏酶抑制剂复合物并重新激活RNaseH。此外,我们显示,也可以通过短RNA三聚体输入来改造RNase H功能,从而从非特异的DNA引导的酶转变为信息性且可编程的RNA引导的酶。可编程RNA识别和切割的例子说明了这种新的刺激反应系统的潜力。
更新日期:2017-09-20
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