Journal of Biochemistry Advance Access originally published online on January 3, 2009
Journal of Biochemistry 2009 145(4):429-435; doi:10.1093/jb/mvn183
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Concerted Effects of Two Activator Modules on the Group I Ribozyme Reaction
1Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0351; 2PRESTO, Japan Science and Technology Agency; 3Graduate School of Biostudies, Kyoto University, Kyoto 606-8502; 4Department of Basic Medical Sciences, Institute of Medical Science, The University of Tokyo, Tokyo 108-8639; and 5ICORP, Japan Science and Technology Agency, Japan
*To whom correspondence should be addressed. Tel: +81-75-753-3995; Fax: +81-75-753-3996; E-mail: tan{at}kuchem.kyoto-u.ac.jp
Received November 17, 2008; Accepted November 28, 2008
| Abstract |
|---|
Group I intron ribozymes have a modular architecture and structural elements essential for catalysis. The elements are located in the conserved modular domain P3–P7 that is stabilized by another conserved module, P4–P6. It has been reported that artificial modules can complement the function of the native P4–P6. To exploit the modular architecture of group I ribozyme, we have constructed a hybrid ribozyme by attaching an artificial activator module to the wild-type T4 td ribozyme. Kinetic analysis of the hybrid ribozyme revealed that the artificial module and P4–P6 have unusual positive and negative concerted effects in activating the ribozyme.
Key Words: activator, group I, intron, modular engineering, ribozyme
Abbreviations: WT, Wild-type