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首页> 外文期刊>Molecular Microbiology >The trp RNA-binding attenuation protein (TRAP) of Bacillus subtilis regulates translation initiation of ycbK, a gene encoding a putative efflux protein, by blocking ribosome binding
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The trp RNA-binding attenuation protein (TRAP) of Bacillus subtilis regulates translation initiation of ycbK, a gene encoding a putative efflux protein, by blocking ribosome binding

机译:枯草芽孢杆菌的trp RNA结合减毒蛋白(TRAP)通过阻止核糖体结合来调节ycbK的翻译起始,ycbK是编码假定的外排蛋白的基因。

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摘要

Expression of the Bacillus subtilis tryptophan biosynthetic genes trpEDCFBA and trpG, as well as a putative tryptophan transport gene (trpP), are regulated in response to tryptophan by the trp RNA-binding attenuation protein (TRAP). TRAP regulates expression of these genes by transcription attenuation and translation control mechanisms. Here we show that TRAP also regulates translation of ycbK, a gene that encodes a protein with similarities to known efflux proteins. As a likely TRAP-binding site consisting of 11 NAG repeats overlaps the ycbK translation initiation region, experiments were carried out to determine whether TRAP regulates translation of ycbK. TRAP was observed to regulate expression of a ycbK'-'lacZ translational fusion 20-fold in response to tryptophan. Binding studies indicated that TRAP binds to the ycbK transcript with high affinity and specificity. Footprint studies revealed that the central seven triplet repeats were protected by bound TRAP, while toeprint results suggest that nine triplet repeats contribute to TRAP binding. Additional toeprint and in vitro translation analyses demonstrated that bound TRAP regulates YcbK synthesis by blocking ribosome binding. We also identified two dipeptide coding minigenes between the Shine-Dalgarno sequence and start codon of ycbK. Expression of one of the minigenes modestly interfered with translation of ycbK.
机译:枯草芽孢杆菌色氨酸生物合成基因trpEDCFBA和trpG的表达,以及推定的色氨酸转运基因(trpP),通过色氨酸RNA结合减弱蛋白(TRAP)响应色氨酸而受到调节。 TRAP通过转录衰减和翻译控制机制调节这些基因的表达。在这里,我们显示TRAP还调节ycbK的翻译,ycbK是一种编码与已知外排蛋白相似的蛋白质的基因。由于可能的由11个NAG重复序列组成的TRAP结合位点与ycbK翻译起始区域重叠,因此进行了实验以确定TRAP是否调节ycbK的翻译。观察到TRAP调节色氨酸响应的ycbK'-'lacZ翻译融合的表达20倍。结合研究表明TRAP以高亲和力和特异性与ycbK转录本结合。足迹研究表明,中央的七个三联体重复序列受结合的TRAP保护,而脚印结果表明九个三联体重复序列有助于TRAP结合。其他脚印和体外翻译分析表明,结合的TRAP通过阻断核糖体结合来调节YcbK的合成。我们还确定了Shine-Dalgarno序列和ycbK的起始密码子之间的两个二肽编码小基因。小基因之一的表达适度地干扰了ycbK的翻译。

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