Leipold R J, Morgan R W, Dhurjati P
Department of Chemical Engineering, University of Delaware, Newark 19716.
Biochem Biophys Res Commun. 1995 Jan 5;206(1):393-400. doi: 10.1006/bbrc.1995.1054.
Specialized ribosomes carry a mutant anti-Shine-Dalgarno region that disrupts the complementary base pairing that stabilizes the translation initiation complex with E. coli mRNAs. It has been reported that production of specialized ribosomes does not cause the inhibition of chromosomal rRNA synthesis that follows production of wild-type ribosomes. We proposed that enabling translation on specialized ribosomes by providing mRNA with a complementary mutation in the Shine-Dalgarno region would restore feedback regulation and inhibit chromosomal rRNA synthesis. With both our system and the system studied previously, we saw feedback regulation regardless of whether the specialized ribosomes were translating. As reported previously, transcription from plasmid-borne promoters decreased as chromosomal rRNA synthesis was repressed, suggesting that the lambda PL and tac promoters may be sensitive to the effector(s) of feedback regulation.
特殊核糖体携带一个突变的抗Shine-Dalgarno区域,该区域会破坏与大肠杆菌mRNA稳定翻译起始复合物的互补碱基配对。据报道,特殊核糖体的产生不会像野生型核糖体产生后那样导致染色体rRNA合成的抑制。我们提出,通过在Shine-Dalgarno区域为mRNA提供互补突变来实现特殊核糖体上的翻译,将恢复反馈调节并抑制染色体rRNA合成。在我们的系统和之前研究的系统中,无论特殊核糖体是否在翻译,我们都观察到了反馈调节。如先前报道,随着染色体rRNA合成受到抑制,来自质粒携带启动子的转录会减少,这表明λPL和tac启动子可能对反馈调节的效应物敏感。