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大肠杆菌中编码释放因子RF3的基因的定位与特性分析

Localization and characterization of the gene encoding release factor RF3 in Escherichia coli.

作者信息

Grentzmann G, Brechemier-Baey D, Heurgue V, Mora L, Buckingham R H

机构信息

Unité de Recherche Associée 1139 du Centre National de la Recherche Scientifique, Institut de Biologie Physico-Chimique, Paris, France.

出版信息

Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5848-52. doi: 10.1073/pnas.91.13.5848.

Abstract

Two protein release factors (RFs) showing codon specificity, RF1 and RF2, are known to be required for polypeptide chain termination in Escherichia coli. A third protein component has also been described that stimulates termination in vitro, but it has remained uncertain whether this protein, RF3, participates in termination in vivo or is essential to cell growth. We report (i) the purification and N-terminal sequencing of RF3; (ii) the isolation of transposon insertion mutants similar to miaD, a suppressor of a leaky UAA mutation affecting the gene miaA, leading to enhanced nonsense suppression; (iii) the localization of the affected gene on the physical map of the chromosome; and (iv) the cloning and sequencing of the wild-type gene, providing proof that it encodes the factor RF3. We designate the gene prfC. Two transposon insertions were shown to interrupt the coding sequence of prfC, at codons 287 and 426. The enhanced nonsense suppression in the insertion mutants shows that the product participates in termination in vivo. The isolation of such mutants strongly suggests that the gene product is not essential to cell viability, though cell growth is affected. RF3 is a protein with a molecular weight of 59,460 containing 528 amino acids and displays much similarity to elongation factor EF-G, a GTP binding protein necessary for ribosomal translocation, and other GTP binding proteins known or thought to interact with the ribosome.

摘要

已知在大肠杆菌中,多肽链终止需要两种具有密码子特异性的蛋白质释放因子(RFs),即RF1和RF2。还描述了第三种蛋白质成分,它在体外刺激终止,但该蛋白质RF3是否参与体内终止或对细胞生长至关重要仍不确定。我们报告了:(i)RF3的纯化和N端测序;(ii)分离出与miaD相似的转座子插入突变体,miaD是影响基因miaA的渗漏UAA突变的抑制子,导致增强的无义抑制;(iii)将受影响的基因定位在染色体的物理图谱上;以及(iv)野生型基因的克隆和测序,证明它编码因子RF3。我们将该基因命名为prfC。两个转座子插入显示在密码子287和426处中断prfC的编码序列。插入突变体中增强的无义抑制表明该产物参与体内终止。此类突变体的分离强烈表明该基因产物对细胞活力不是必需的,尽管细胞生长受到影响。RF3是一种分子量为59,460的蛋白质,含有528个氨基酸,与延伸因子EF-G(核糖体转位所需的一种GTP结合蛋白)以及其他已知或被认为与核糖体相互作用的GTP结合蛋白有很多相似之处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ba8/44094/d1febdc5ad7c/pnas01135-0124-a.jpg

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