Li Lei, Wang Ching C
Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94143-2280, USA.
J Biol Chem. 2004 Apr 9;279(15):14656-64. doi: 10.1074/jbc.M309879200. Epub 2004 Jan 13.
The 5'-untranslated region (5'-UTR) of an mRNA plays an important role in translation initiation in eukaryotes. A minimal length of about 20 nucleotides is required to prevent leaky ribosome scanning. In one of the most primitive eukaryotes, Giardia lamblia, however, the mRNAs have 5'-UTRs mostly in the range of 0 to 14 nucleotides without a conserved sequence, which raises the question on how the ribosome could effectively scan such short 5'-UTRs for an accurate initiation of translation. In the present study, we expressed capped transcripts of luciferase gene in Giardia trophozoites via transfection and observed that when the 5'-UTR of the transcript was lengthened from 9 to 21 nucleotides, there was a corresponding decrease of translation efficiency. Conversely, shortening of the 5'-UTR from nine nucleotides down to a single nucleotide did not result in any reduced translation or leaky scanning. Translation appeared to initiate exclusively from the first initiation codon located downstream from the cap. Experimental evidence indicated also that a stem-loop structure immediately downstream from the initiation codon exerted significant inhibition on translation initiation when the 5'-UTR consisted of less than seven nucleotides. This inhibitory effect was abolished by increasing the distance between the stem-loop and the cap-G structure either upstream or downstream from the start codon, thus suggesting a spatial requirement for effective ribosome recruitment. Overall, our results suggest an absence of ribosome scanning for AUG in initiating translation in Giardia. A capped mRNA with a single nucleotide leader is apparently sufficient for recruiting ribosome and initiating translation.
信使核糖核酸(mRNA)的5′非翻译区(5′-UTR)在真核生物的翻译起始过程中发挥着重要作用。为防止核糖体的漏扫描,需要大约20个核苷酸的最小长度。然而,在最原始的真核生物之一——蓝氏贾第鞭毛虫中,mRNA的5′-UTR大多在0至14个核苷酸范围内,且没有保守序列,这就引发了一个问题:核糖体如何有效地扫描如此短的5′-UTR以准确起始翻译。在本研究中,我们通过转染在蓝氏贾第鞭毛虫滋养体中表达了荧光素酶基因的加帽转录本,并观察到当转录本的5′-UTR从9个核苷酸延长至21个核苷酸时,翻译效率相应降低。相反,将5′-UTR从9个核苷酸缩短至单个核苷酸并不会导致翻译减少或出现漏扫描。翻译似乎仅从帽下游的第一个起始密码子起始。实验证据还表明,当5′-UTR由少于7个核苷酸组成时,起始密码子紧邻下游的茎环结构对翻译起始具有显著抑制作用。通过增加茎环与起始密码子上游或下游的帽-G结构之间的距离,这种抑制作用被消除,这表明有效招募核糖体存在空间需求。总体而言,我们的结果表明在蓝氏贾第鞭毛虫起始翻译时不存在核糖体对AUG的扫描。具有单个核苷酸前导序列的加帽mRNA显然足以招募核糖体并起始翻译。