Functional characterization of IRESes by an inhibitor of the RNA helicase eIF4A

被引:288
作者
Bordeleau, ME
Mori, A
Oberer, M
Lindqvist, L
Chard, LS
Higa, T
Belsham, GJ
Wagner, G
Tanaka, J
Pelletier, J
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] Univ Ryukyus, Dept Chem Biol & Marine Sci, Okinawa 9030213, Japan
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] AFRC, Inst Anim Hlth, Woking GU24 0NF, Surrey, England
[5] McGill Univ, McGill Canc Ctr, Montreal, PQ H3G 1Y6, Canada
关键词
D O I
10.1038/nchembio776
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
RNA helicases are molecular motors that are involved in virtually all aspects of RNA metabolism. Eukaryotic initiation factor (eIF) 4A is the prototypical member of the DEAD-box family of RNA helicases. It is thought to use energy from ATP hydrolysis to unwind mRNA structure and, in conjunction with other translation factors, it prepares mRNA templates for ribosome recruitment during translation initiation. In screening marine extracts for new eukaryotic translation initiation inhibitors, we identified the natural product hippuristanol. We show here that this compound is a selective and potent inhibitor of eIF4A RNA-binding activity that can be used to distinguish between eIF4A-dependent and -independent modes of translation initiation in vitro and in vivo. We also show that poliovirus replication is delayed when infected cells are exposed to hippuristanol. Our study demonstrates the feasibility of selectively targeting members of the DEAD-box helicase family with small-molecule inhibitors.
引用
收藏
页码:213 / 220
页数:8
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