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枯草芽孢杆菌的色氨酸RNA结合衰减蛋白(TRAP)通过阻止核糖体结合来调节ycbK(一个编码假定外排蛋白的基因)的翻译起始。

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.

作者信息

Yakhnin Helen, Yakhnin Alexander V, Babitzke Paul

机构信息

Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, USA.

出版信息

Mol Microbiol. 2006 Sep;61(5):1252-66. doi: 10.1111/j.1365-2958.2006.05278.x.

Abstract

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.

摘要

枯草芽孢杆菌色氨酸生物合成基因trpEDCFBA和trpG以及一个假定的色氨酸转运基因(trpP)的表达受色氨酸RNA结合衰减蛋白(TRAP)调控以响应色氨酸。TRAP通过转录衰减和翻译控制机制调控这些基因的表达。在此我们表明,TRAP还调控ycbK的翻译,ycbK是一个编码与已知外排蛋白相似蛋白的基因。由于一个由11个NAG重复序列组成的可能的TRAP结合位点与ycbK翻译起始区域重叠,因此开展实验以确定TRAP是否调控ycbK的翻译。观察到TRAP响应色氨酸调控ycbK'-'lacZ翻译融合体的表达达20倍。结合研究表明,TRAP以高亲和力和特异性结合ycbK转录本。足迹研究显示,中央的七个三联体重复序列被结合的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。额外的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控YcbK的合成。我们还在ycbK的Shine-Dalgarno序列和起始密码子之间鉴定出两个二肽编码小基因。其中一个小基因的表达适度干扰了ycbK的翻译。

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