Department of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, Knoxville, Tennessee 37996, USA.
RNA. 2010 Apr;16(4):748-61. doi: 10.1261/rna.2056010. Epub 2010 Feb 23.
Upstream open reading frames (uORFs) are protein coding elements in the 5' leader of messenger RNAs. uORFs generally inhibit translation of the main ORF because ribosomes that perform translation elongation suffer either permanent or conditional loss of reinitiation competence. After conditional loss, reinitiation competence may be regained by, at the minimum, reacquisition of a fresh methionyl-tRNA. The conserved h subunit of Arabidopsis eukaryotic initiation factor 3 (eIF3) mitigates the inhibitory effects of certain uORFs. Here, we define more precisely how this occurs, by combining gene expression data from mutated 5' leaders of Arabidopsis AtbZip11 (At4g34590) and yeast GCN4 with a computational model of translation initiation in wild-type and eif3h mutant plants. Of the four phylogenetically conserved uORFs in AtbZip11, three are inhibitory to translation, while one is anti-inhibitory. The mutation in eIF3h has no major effect on uORF start codon recognition. Instead, eIF3h supports efficient reinitiation after uORF translation. Modeling suggested that the permanent loss of reinitiation competence during uORF translation occurs at a faster rate in the mutant than in the wild type. Thus, eIF3h ensures that a fraction of uORF-translating ribosomes retain their competence to resume scanning. Experiments using the yeast GCN4 leader provided no evidence that eIF3h fosters tRNA reaquisition. Together, these results attribute a specific molecular function in translation initiation to an individual eIF3 subunit in a multicellular eukaryote.
上游开放阅读框(uORFs)是信使 RNA 5' 先导区的蛋白编码元件。uORFs 通常抑制主要 ORF 的翻译,因为进行翻译延伸的核糖体要么永久性地、要么有条件地丧失重新起始的能力。有条件地丧失后,重新起始的能力可能通过至少重新获得新鲜的甲硫氨酰-tRNA 来恢复。拟南芥真核起始因子 3(eIF3)的保守 h 亚基减轻了某些 uORFs 的抑制作用。在这里,我们通过结合拟南芥 AtbZip11(At4g34590)和酵母 GCN4 的突变 5' 先导区的基因表达数据和野生型及 eif3h 突变体植物中翻译起始的计算模型,更精确地定义了这是如何发生的。在 AtbZip11 的四个系统发育保守的 uORFs 中,有三个抑制翻译,而一个则具有反抑制作用。eIF3h 的突变对 uORF 起始密码子的识别没有重大影响。相反,eIF3h 支持 uORF 翻译后的有效重新起始。模型表明,在突变体中,uORF 翻译过程中重新起始能力的永久性丧失比在野生型中更快。因此,eIF3h 确保了一部分正在翻译 uORF 的核糖体保留其重新扫描的能力。使用酵母 GCN4 先导进行的实验没有提供证据表明 eIF3h 促进 tRNA 的重新获得。总之,这些结果将特定的翻译起始分子功能归因于多细胞真核生物中的单个 eIF3 亚基。