Ivanov Ivaylo P, Gesteland Raymond F, Atkins John F
RNA. 2006 Mar;12(3):332-7. doi: 10.1261/rna.2245906. Epub 2006 Jan 23.
An autoregulatory translational shift to the +1 frame is required for the expression of ornithine decarboxylase antizyme from fungi to mammals. In most eukaryotes, including all vertebrates and a majority of the studied fungi/yeast, the site on antizyme mRNA where the shift occurs is UCC-UGA. The mechanism of the frameshift on this sequence likely involves nearly universal aspects of the eukaryotic translational machinery. Nevertheless, a mammalian antizyme frameshift cassette yields predominantly -2 frameshift in Saccharomyces cerevisiae, instead of the +1 in mammals. The recently identified endogenous S. cerevisiae antizyme mRNA has an atypical shift site: UGC-GCG-UGA. It is shown here that endogenous S. cerevisiae antizyme frameshifting is +1 rather than -2. We discuss how antizyme frameshifting in budding yeasts exploits peculiarities of their tRNA balance, and relate this to prior studies on Ty frameshifting.
从真菌到哺乳动物,鸟氨酸脱羧酶抗酶的表达需要向+1读码框进行自调控翻译移码。在大多数真核生物中,包括所有脊椎动物以及大部分已研究的真菌/酵母,抗酶mRNA上发生移码的位点是UCC-UGA。该序列上移码的机制可能涉及真核生物翻译机制的几乎普遍特征。然而,哺乳动物抗酶移码盒在酿酒酵母中主要产生-2移码,而非在哺乳动物中的+1移码。最近鉴定出的内源性酿酒酵母抗酶mRNA具有一个非典型的移码位点:UGC-GCG-UGA。本文表明内源性酿酒酵母抗酶的移码是+1而非-2。我们讨论了芽殖酵母中抗酶移码如何利用其tRNA平衡的特性,并将其与之前关于Ty移码的研究联系起来。