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大肠杆菌fdhF“硒代半胱氨酸插入序列”(SECIS)中的一个序列在没有硒的情况下也能发挥作用。

A sequence in the Escherichia coli fdhF "selenocysteine insertion Sequence" (SECIS) operates in the absence of selenium.

作者信息

Liu Z, Reches M, Engelberg-Kulka H

机构信息

Department of Molecular Biology, Hebrew University-Hadassah Medical School, Jerusalem, 91120, Israel.

出版信息

J Mol Biol. 1999 Dec 17;294(5):1073-86. doi: 10.1006/jmbi.1999.3307.

Abstract

The UGA codon context of the Escherichia coli fdhF mRNA includes an element called the selenocysteine insertion sequence (SECIS) that is responsible for the UGA-directed incorporation of the amino acid selenocysteine into a protein. Here, we describe an extended fdhF SECIS that includes the information for an additional function: the prevention of UGA readthrough under conditions of selenium deficiency. This information is contained in a short mRNA region consisting of a single C residue adjacent to the UGA on its downstream side, and an additional segment consisting of the six nucleotides immediately upstream from it. These two regions act independently and additively, and probably through different mechanisms. The single C residue acts as itself; the upstream region acts at the level of the two amino acids, arginine and valine, for which it codes. These two codons at the 5' side of the UGA correspond to the ribosomal E and P sites. Here, we present a model for the E. coli fdhF SECIS as a multifunctional RNA structure containing three functional elements. Depending on the availability of selenium, the SECIS enables one of two alternatives for the translational machinery: either selenocysteine incorporation into a polypeptide or termination of the polypeptide chain.

摘要

大肠杆菌fdhF mRNA的UGA密码子上下文包含一个称为硒代半胱氨酸插入序列(SECIS)的元件,该元件负责将氨基酸硒代半胱氨酸以UGA指导的方式掺入蛋白质中。在此,我们描述了一种扩展的fdhF SECIS,它包含另一种功能的信息:在硒缺乏条件下防止UGA通读。该信息包含在一个短的mRNA区域中,该区域由位于UGA下游侧的单个C残基以及紧接其上游的六个核苷酸组成的另一段组成。这两个区域独立且累加地起作用,可能通过不同的机制。单个C残基以其自身起作用;上游区域在其编码的两种氨基酸精氨酸和缬氨酸的水平上起作用。UGA 5'侧的这两个密码子对应于核糖体E和P位点。在此,我们提出了一种大肠杆菌fdhF SECIS的模型,它是一种包含三个功能元件的多功能RNA结构。根据硒的可用性,SECIS使翻译机制有两种选择之一:要么将硒代半胱氨酸掺入多肽中,要么终止多肽链。

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