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CCC.UGA:大肠杆菌中核糖体移码的一个新位点。

CCC.UGA: a new site of ribosomal frameshifting in Escherichia coli.

作者信息

de Smit M H, van Duin J, van Knippenberg P H, van Eijk H G

机构信息

Department of Biochemistry, Gorlaeus Laboratories, Leiden University, The Netherlands.

出版信息

Gene. 1994 May 27;143(1):43-7. doi: 10.1016/0378-1119(94)90602-5.

Abstract

To activate expression of a human transferrin (Tf)-encoding cDNA in Escherichia coli by translational coupling, it was placed in an expression plasmid downstream from a 5'-terminal fragment from the replicase (R)-encoding gene of bacteriophage MS2. The resulting construct was found to produce, besides the desired Tf, a protein with the mobility of a fusion product (RTf) of the N-terminal R fragment and Tf. Analysis of available mutants showed that this fusion results from +1 ribosomal frameshifting at the end of the R reading frame. This region contains the sequence, CCC.UGA, suggesting that before termination occurs, tRNA(Pro) may dislodge from the CCC codon and reassociate with the +1 triplet CCU. By further site-directed mutagenesis, we demonstrate that both the CCC codon and the termination codon are indeed required for the observed 2-4% frameshifting. When either triplet is changed, the frequency of frameshifting drops to 0.3% or less. These results classify CCC.UGA as a new '+1 shifty stop'.

摘要

为了通过翻译偶联在大肠杆菌中激活人转铁蛋白(Tf)编码cDNA的表达,将其置于噬菌体MS2复制酶(R)编码基因5'末端片段下游的表达质粒中。结果发现,除了所需的Tf外,所得构建体还产生一种具有N末端R片段和Tf融合产物(RTf)迁移率的蛋白质。对现有突变体的分析表明,这种融合是由于R阅读框末端的+1核糖体移码造成的。该区域包含序列CCC.UGA,这表明在终止发生之前,tRNA(Pro)可能从CCC密码子上脱离并与+1三联体CCU重新结合。通过进一步的定点诱变,我们证明CCC密码子和终止密码子确实是观察到的2-4%移码所必需的。当任何一个三联体发生变化时,移码频率降至0.3%或更低。这些结果将CCC.UGA归类为一种新的“+1移码终止”。

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