硒代半胱氨酸插入对哺乳动物细胞系停止密码子抑制的定量测试系统。

H Kollmus, J E McCarthy, L Flohé
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引用次数: 0

摘要

设计了一种方便的测试系统来研究硒半胱氨酸插入序列(SECIS)的效率,该序列负责硒半胱氨酸与哺乳动物硒蛋白的共翻译结合。它包括一个表达载体,其中lacZ和luc基因被帧内TGA停止密码子分开。编码区之后是一个多克隆区,允许交换假定的SECIS元素。与硒代半胱氨酸结合相关的终止密码子抑制很容易根据相对荧光素酶活性测量来估计,从而提供了一种测量SECIS效率的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Test system for quantification of stop codon suppression by selenocysteine insertion in mammalian cell lines.

A convenient test system was designed to investigate the efficiencies of selenocysteine inserting sequences (SECIS) responsible for the cotranslational incorporation of selenocysteine into selenoproteins of mammals. It comprises an expression vector in which the lacZ and luc genes are separated by an in-frame TGA stop codon. The coding regions are followed by a multicloning region allowing exchange of putative SECIS elements. Stop codon suppression associated with selenocysteine incorporation is readily estimated on the basis of relative luciferase activity measurements, thus providing a measure of SECIS efficiency.

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