Matsuda Daiki, Dreher Theo W
Department of Microbiology, Oregon State University, Corvallis, OR 97331-3804, USA.
Virology. 2004 Mar 30;321(1):36-46. doi: 10.1016/j.virol.2003.10.023.
Many positive stand RNA viral genomes lack the poly(A) tail that is characteristic of cellular mRNAs and that promotes translation in cis. The 3' untranslated regions (UTRs) of such genomes are expected to provide similar translation-enhancing properties as a poly(A) tail, yet the great variety of 3' sequences suggests that this is accomplished in a range of ways. We have identified a translational enhancer present in the 3' UTR of Turnip yellow mosaic virus (TYMV) RNA using luciferase reporter RNAs with generic 5' sequences transfected into plant cells. The 3' terminal 109 nucleotides comprising the tRNA-like structure (TLS) and an upstream pseudoknot (UPSK) act in synergy with a 5'-cap to enhance translation, with a minor contribution in stabilizing the RNA. Maximum enhancement requires that the RNA be capable of aminoacylation, but either the native valine or engineered methionine is acceptable. Mutations that decrease the affinity for translation elongation factor eEF1A (but also diminish aminoacylation efficiency) strongly decrease translational enhancement, suggesting that eEF1A is mechanistically involved. The UPSK seems to act as an important, though nonspecific, spacer element ensuring proper presentation of a functional TLS. Our studies have uncovered a novel type of translational enhancer and a new role for a plant viral TLS.
许多正义链RNA病毒基因组缺乏细胞mRNA所特有的聚腺苷酸尾巴,而聚腺苷酸尾巴能顺式促进翻译。这类基因组的3'非翻译区(UTR)预计能提供与聚腺苷酸尾巴类似的翻译增强特性,然而3'序列的多样性表明这是以多种方式实现的。我们使用转染到植物细胞中的具有通用5'序列的荧光素酶报告RNA,在芜菁黄花叶病毒(TYMV)RNA的3'UTR中鉴定出一种翻译增强子。包含类tRNA结构(TLS)和上游假结(UPSK)的3'末端109个核苷酸与5'-帽协同作用以增强翻译,在稳定RNA方面贡献较小。最大程度的增强要求RNA能够进行氨酰化,但天然缬氨酸或工程化甲硫氨酸均可接受。降低对翻译延伸因子eEF1A亲和力(但也降低氨酰化效率)的突变会强烈降低翻译增强,这表明eEF1A在机制上参与其中。UPSK似乎起着重要的、尽管是非特异性的间隔元件的作用,确保功能性TLS的正确呈现。我们的研究发现了一种新型的翻译增强子以及植物病毒TLS的新作用。