THE IS10 TRANSPOSASE MESSENGER-RNA IS DESTABILIZED DURING ANTISENSE RNA CONTROL

被引:68
作者
CASE, CC [1 ]
SIMONS, EL [1 ]
SIMONS, RW [1 ]
机构
[1] UNIV CALIF LOS ANGELES,INST MOLEC BIOL,LOS ANGELES,CA 90024
关键词
antisense RNA; IS10; mRNA stability; ribonuclease III; transposon;
D O I
10.1002/j.1460-2075.1990.tb08234.x
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 stability is an important component of gene expression, and antisense RNAs have been proposed to alter target RNA stability. We show here that the IS10 transposase mRNA, RNA-IN, is rendered unstable during control by the IS10 antisense RNA, RNA-OUT. Destabilization requires RNA-OUT/RNA-IN pairing and ribonuclease III cleavage. Independent of such cleavage, RNA-OUT is rendered unstable through disruption of its secondary structure. Pairing has no other obvious effects on RNA-IN transcription or stability. Nevertheless, RNA-IN destabilization is not required for antisense control in vivo. In the accompanying paper [Ma, C. and Simons, R.W. (1990) EMBO J., 9, 1267-1274] we show that pairing blocks ribosome binding to RNA-IN. Were it not for control at this level, destabilization would play a more prominent role.
引用
收藏
页码:1259 / 1266
页数:8
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