Karginov Timofey A, Pastor Daniel Parviz Hejazi, Semler Bert L, Gomez Christopher M
Department of Neurology, University of Chicago, Chicago, IL, USA.
Department of Microbiology & Molecular Genetics, School of Medicine, University of California, Irvine, CA, USA.
Trends Genet. 2017 Feb;33(2):129-142. doi: 10.1016/j.tig.2016.11.007. Epub 2016 Dec 21.
Our understanding of gene expression has come far since the 'one-gene one-polypeptide' hypothesis proposed by Beadle and Tatum. In this review, we address the gradual recognition that a growing number of polycistronic genes, originally discovered in viruses, are being identified within the mammalian genome, and that these may provide new insights into disease mechanisms and treatment. We carried out a systematic literature review identifying 13 mammalian genes for which there is evidence for polycistronic expression via translation through an internal ribosome entry site (IRES). Although the canonical mechanism of translation initiation has been studied extensively, here we highlight a process of noncanonical translation, IRES-mediated translation, that is a growing source for understanding complex inheritance, the elucidation of disease mechanisms, and the discovery of novel therapeutic targets. Identification of additional polycistronic genes may provide new insights into disease therapy and allow for new discoveries of both translational and disease mechanisms.
自从比德尔和塔图姆提出“一个基因一种多肽”假说来,我们对基因表达的理解已经有了长足的进步。在这篇综述中,我们阐述了这样一个逐渐形成的认识:最初在病毒中发现的越来越多的多顺反子基因正在哺乳动物基因组中被识别出来,而这些基因可能为疾病机制和治疗提供新的见解。我们进行了一项系统的文献综述,确定了13个哺乳动物基因,有证据表明它们通过内部核糖体进入位点(IRES)进行翻译从而实现多顺反子表达。尽管翻译起始的经典机制已经得到了广泛研究,但在这里我们强调一种非经典翻译过程,即IRES介导的翻译,它正日益成为理解复杂遗传、阐明疾病机制以及发现新型治疗靶点的一个来源。识别更多的多顺反子基因可能为疾病治疗提供新的见解,并有助于发现翻译机制和疾病机制。