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干扰素-γ mRNA的动态重折叠使其能够作为PKR激活剂和翻译模板发挥作用。

Dynamic refolding of IFN-gamma mRNA enables it to function as PKR activator and translation template.

作者信息

Cohen-Chalamish Smadar, Hasson Anat, Weinberg Dahlia, Namer Lise Sarah, Banai Yona, Osman Farhat, Kaempfer Raymond

机构信息

Department of Biochemistry and Molecular Biology, Institute for Medical Research Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Nat Chem Biol. 2009 Dec;5(12):896-903. doi: 10.1038/nchembio.234. Epub 2009 Oct 4.

Abstract

Interferon-gamma mRNA activates the RNA-dependent protein kinase PKR, which in turn strongly attenuates translation of interferon-gamma mRNA. Unlike riboswitches restricted to noncoding regions, the interferon-gamma RNA domain that activates PKR comprises the 5' UTR and 26 translated codons. Extensive interferon-gamma coding sequence is thus dedicated to activating PKR and blocking interferon-gamma synthesis. This implies that the PKR activator is disrupted by ribosomes during translation initiation and must refold promptly to restore PKR activation. The activator structure harbors an essential kink-turn, probably to allow formation of a pseudoknot that is critical for PKR activation. Three indispensable short helices, bordered by orientation-sensitive base pairs, align with the pseudoknot stem, generating RNA helix of sufficient length to activate PKR. Through gain-of-function mutations, we show that the RNA activator can adopt alternative conformations that activate PKR. This flexibility promotes efficient refolding of interferon-gamma mRNA, which is necessary for its dual function as translation template and activator of PKR, and which thus prevents overexpression of this inflammatory cytokine.

摘要

干扰素-γ信使核糖核酸(mRNA)激活依赖RNA的蛋白激酶PKR,而PKR反过来又会强烈减弱干扰素-γ mRNA的翻译。与局限于非编码区的核糖开关不同,激活PKR的干扰素-γ RNA结构域包括5'非翻译区(UTR)和26个编码密码子。因此,大量的干扰素-γ编码序列专门用于激活PKR并阻断干扰素-γ的合成。这意味着PKR激活剂在翻译起始过程中会被核糖体破坏,并且必须迅速重新折叠以恢复PKR激活。激活剂结构含有一个必不可少的扭结环,可能是为了允许形成对PKR激活至关重要的假结。三个不可或缺的短螺旋,由方向敏感的碱基对界定,与假结茎对齐,产生足够长度的RNA螺旋以激活PKR。通过功能获得性突变,我们表明RNA激活剂可以采用激活PKR的替代构象。这种灵活性促进了干扰素-γ mRNA的有效重新折叠,这对于其作为翻译模板和PKR激活剂的双重功能是必要的,从而防止这种炎性细胞因子的过度表达。

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