Akashi Hideo, Kawasaki Hiroaki, Kim Won Jong, Akaike Toshihiro, Taira Kazunari, Maruyama Atsushi
Department of Chemistry and Biotechnology, School of Engineering, The University of Tokyo, Hongo, Tokyo 113-8656, Japan.
J Biochem. 2002 May;131(5):687-92. doi: 10.1093/oxfordjournals.jbchem.a003152.
The activity of a hammerhead ribozyme (Rz) in vivo depends on several factors, such as abundance, stability, and accessibility of Rz to its target mRNA. Among these factors, accessibility is believed to be the rate-limiting factor for Rz-mediated cleavage in vivo. As Rz and its substrate RNA are negatively charged, we examined whether cellular RNA-interacting proteins or artificial polycations might improve the accessibility of Rz to its substrate RNA. Specifically, we examined the effects of two kinds of cationic comb-type copolymer, alphaPLL-g-Dex, and a cellular RNA helicase on the accessibility of Rz to a model structured RNA in vitro. The cleavage activity of Rz was slightly enhanced by alphaPLL-g-Dex, probably due to an acceleration of the association/dissociation rate. And also, the RNA helicase-bound hybrid-Rz could cleave the target substrate at a significantly higher rate due to its unwinding activity for the duplex RNA substrate. These approaches should be useful in the development of efficient gene-inactivating reagents in the post-genomic era.
锤头状核酶(Rz)在体内的活性取决于几个因素,如Rz的丰度、稳定性及其与靶标mRNA的可及性。在这些因素中,可及性被认为是Rz在体内介导切割的限速因素。由于Rz及其底物RNA带负电荷,我们研究了细胞RNA相互作用蛋白或人工聚阳离子是否能提高Rz与其底物RNA的可及性。具体而言,我们研究了两种阳离子梳型共聚物αPLL-g-Dex和一种细胞RNA解旋酶对Rz在体外与模型结构化RNA可及性的影响。αPLL-g-Dex使Rz的切割活性略有增强,这可能是由于缔合/解离速率加快所致。此外,与RNA解旋酶结合的杂交Rz由于其对双链RNA底物的解旋活性,能够以显著更高的速率切割靶标底物。这些方法在基因组时代高效基因失活试剂的开发中应会很有用。