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删除大肠杆菌假尿苷合酶基因truB会阻止体内tRNA中假尿苷55的形成,不影响指数生长,但在与野生型细胞竞争时会带来强烈的选择劣势。

Deletion of the Escherichia coli pseudouridine synthase gene truB blocks formation of pseudouridine 55 in tRNA in vivo, does not affect exponential growth, but confers a strong selective disadvantage in competition with wild-type cells.

作者信息

Gutgsell N, Englund N, Niu L, Kaya Y, Lane B G, Ofengand J

机构信息

Department of Biochemistry and Molecular Biology, University of Miami School of Medicine, Florida 33101, USA.

出版信息

RNA. 2000 Dec;6(12):1870-81. doi: 10.1017/s1355838200001588.

Abstract

Previous work from this laboratory (Nurse et al., RNA, 1995, 1:102-112) established that TruB, a pseudouridine (psi) synthase from Escherichia coli, was able to make psi55 in tRNA transcripts but not in transcripts of full-length or fragmented 16S or 23S ribosomal RNAs. By deletion of the truB gene, we now show that TruB is the only protein in E. coli able to make psi55 in vivo. Lack of TruB and psi55 did not affect the exponential growth rate but did confer a strong selective disadvantage on the mutant when it was competed against wild-type. The negative selection did not appear to be acting at either the exponential or stationary phase. Transformation with a plasmid vector conferring carbenicillin resistance and growth in carbenicillin markedly increased the selective disadvantage, as did growth at 42 degrees C, and both together were approximately additive such that three cycles of competitive growth sufficed to reduce the mutant strain to approximately 0.2% of its original value. The most striking finding was that all growth effects could be reversed by transformation with a plasmid carrying a truB gene coding for a D48C mutation in TruB. Direct analysis showed that this mutant did not make psi55 under the conditions of the competition experiment. Therefore, the growth defect due to the lack of TruB must be due to the lack of some other function of the protein, possibly an RNA chaperone activity, but not to the absence of psi55.

摘要

该实验室先前的研究工作(Nurse等人,《RNA》,1995年,第1卷:102 - 112页)证实,大肠杆菌中的假尿苷(ψ)合酶TruB能够在tRNA转录本中生成ψ55,但在全长或片段化的16S或23S核糖体RNA转录本中则不能。通过缺失truB基因,我们现在表明TruB是大肠杆菌中唯一能够在体内生成ψ55的蛋白质。缺乏TruB和ψ55并不影响指数生长速率,但当突变体与野生型竞争时,确实赋予了突变体强大的选择劣势。负选择似乎在指数期或稳定期都不起作用。用赋予羧苄青霉素抗性的质粒载体转化并在羧苄青霉素中生长显著增加了选择劣势,在42℃下生长也是如此,两者共同作用大致呈累加效应,以至于三个循环的竞争性生长足以将突变菌株减少到其原始值的约0.2%。最显著的发现是,所有生长效应都可以通过用携带编码TruB中D48C突变的truB基因的质粒转化来逆转。直接分析表明,该突变体在竞争实验条件下不产生ψ55。因此,由于缺乏TruB导致的生长缺陷一定是由于该蛋白质的某些其他功能缺失,可能是一种RNA伴侣活性,而不是由于缺乏ψ55。

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