Length variation of helix III in a hammerhead ribozyme and its influence on cleavage activity

被引:4
作者
Hammann, C
Martinez, E
Moosbauer, J
Hormes, R
Tabler, M
机构
[1] Fdn Res & Technol Hellas, Inst Mol Biol & Biotechnol, GR-71110 Iraklion, Greece
[2] Deutsch Krebsforschungszentrum, Forsch Schwerpunkt Angew Tumorvirol, D-6900 Heidelberg, Germany
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 1999年 / 9卷 / 01期
关键词
D O I
10.1089/oli.1.1999.9.25
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
The previously described HIV-1 directed hammerhead ribozyme 2as-Rz12 can form with its target RNA 2s helices I and III of 128 and 278 base pairs (bp), A series of derivatives was made in which helix III was truncated to 8, 5, 4, 3, and 2 nucleotides (nt). These asymmetric hammerhead ribozymes were tested for in vitro cleavage and for inhibition of HIV-1 replication in human cells, Truncation of helix III to 8 bp did not affect the in vitro cleavage potential of the parental catalytic antisense RNA 2as-Rz12. Further truncation of helix III led to decreased cleavage rates, with no measurable cleavage activity for the 2 bp construct. All catalytically active constructs showed complex cleavage kinetics. Three kinetic subpopulations of ribozyme-substrate complexes could be discriminated that were cleaved with fast or slow rates or not at all. Gel purification of preformed ribozyme-substrate complexes led to a significant increase in cleavage rates. However, the complex cleavage pattern remained. In mammalian cells, the helix III-truncated constructs showed the same but no increased inhibitory effect of the comparable antisense RNA on HIV-1 replication.
引用
收藏
页码:25 / 31
页数:7
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