Wiklund Lisa, Sokolowski Marcus, Carlsson Anette, Rush Margaret, Schwartz Stefan
Department of Medical Biochemistry and Microbiology, Biomedical Center, Uppsala University, Husargatan 3, Box 582, 751 23 Uppsala, Sweden.
J Biol Chem. 2002 Oct 25;277(43):40462-71. doi: 10.1074/jbc.M205929200. Epub 2002 Jul 29.
The human papillomavirus type 1 (HPV-1) late mRNAs contain a 57-nucleotide adenosine- and uridine-rich RNA instability element termed h1ARE in their late 3' untranslated regions. Here we show that five sequence motifs in the h1ARE (named I-V) affect the mRNA half-life in an additive manner. The minimal inhibitory sequence in motifs I and II was mapped to UAUUUAU, and the minimal inhibitory sequence in motifs III-V was mapped to UAUUUUUAU. We also provide evidence that the same motifs in the AU-RNA instability element inhibit mRNA translation, an effect that was entirely dependent on the presence of a poly(A) tail on the mRNA. Additional experiments demonstrated that the h1ARE interacted directly with the poly(A)-binding protein, suggesting that the h1ARE inhibits translation by interfering with the function of the poly(A)-binding protein.
1型人乳头瘤病毒(HPV-1)晚期mRNA在其3'非翻译区含有一个57个核苷酸的富含腺苷和尿苷的RNA不稳定元件,称为h1ARE。我们在此表明,h1ARE中的五个序列基序(命名为I-V)以累加方式影响mRNA半衰期。基序I和II中的最小抑制序列定位为UAUUUAU,基序III-V中的最小抑制序列定位为UAUUUUUAU。我们还提供证据表明,AU-RNA不稳定元件中的相同基序抑制mRNA翻译,这种效应完全依赖于mRNA上poly(A)尾的存在。额外的实验表明,h1ARE直接与聚腺苷酸结合蛋白相互作用,提示h1ARE通过干扰聚腺苷酸结合蛋白的功能来抑制翻译。