Chandler M, Fayet O
Microbiologie et Génétique Moléculaire (UPR 9007), CNRS, Toulouse, France.
Mol Microbiol. 1993 Feb;7(4):497-503. doi: 10.1111/j.1365-2958.1993.tb01140.x.
The expression of an increasing number of genes of both prokaryotic and eukaryotic origin has been shown to be regulated at the translational level by programmed (sequence-specific) ribosomal frameshifting. Among these are the bacterial insertion sequences IS1 and two members of the widely distributed IS3-family, IS150 and IS911. Frameshifting provides a means of specifying several proteins with different functions using a minimum of genetic information. In this review, we survey present understanding of the way in which frameshifting is integrated into the overall control of transposition activity in these elements.
越来越多的原核和真核生物来源的基因表达已被证明在翻译水平上受程序性(序列特异性)核糖体移码调控。其中包括细菌插入序列IS1以及广泛分布的IS3家族的两个成员IS150和IS911。移码提供了一种使用最少的遗传信息来指定几种具有不同功能蛋白质的方法。在这篇综述中,我们概述了目前对移码如何整合到这些元件转座活性的整体控制方式的理解。