Brombach M, Pon C L
Mol Gen Genet. 1987 Jun;208(1-2):94-100. doi: 10.1007/BF00330428.
The expression of infC, the structural gene for translational initiation factor IF3, has been studied in different constructs under the control of the lambda PL and tac promoters. The amount of synthesized IF3 has been determined by a quantitative functional test and the levels of IF3-specific mRNA have been estimated. The synthesis of IF3 is strongly enhanced when the unusual AUU initiation codon is changed to AUG by site-directed mutagenesis. Removal of the sequence upstream from the start codon including most of the Shine-Dalgarno sequence, as well as part of a 10 bp region with potential complementarity to an internal region of the 16S rRNA, which is unique to the IF3 mRNA, reduced but did not completely abolish the high expression of infC obtained after introduction of the AUG initiation codon. The level of IF3 mRNA was found to be positively influenced by the presence of the rplT gene in the plasmid downstream from the infC gene. In vivo accumulation of a large excess of IF3, obtained when the infC gene was placed under the control of an incompletely repressed tac promoter, was not accompanied by any noticeable adverse phenotype.
已在λPL和tac启动子控制下的不同构建体中研究了翻译起始因子IF3的结构基因infC的表达。通过定量功能测试确定了合成的IF3量,并估计了IF3特异性mRNA的水平。当通过定点诱变将异常的AUU起始密码子变为AUG时,IF3的合成强烈增强。去除起始密码子上游的序列,包括大部分Shine-Dalgarno序列,以及与16S rRNA内部区域具有潜在互补性的10 bp区域的一部分(这是IF3 mRNA特有的),降低但并未完全消除引入AUG起始密码子后获得的infC的高表达。发现IF3 mRNA的水平受到infC基因下游质粒中rplT基因存在的正向影响。当infC基因置于未完全抑制的tac启动子控制下时获得大量过量的IF3在体内积累,并未伴随任何明显的不良表型。