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

被引:64
作者
Cohen-Chalamish, Smadar [1 ]
Hasson, Anat [1 ]
Weinberg, Dahlia [1 ]
Namer, Lise Sarah [1 ]
Banai, Yona [1 ]
Osman, Farhat [1 ]
Kaempfer, Raymond [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Biochem & Mol Biol, Inst Med Res Israel Canada, IL-91010 Jerusalem, Israel
基金
以色列科学基金会;
关键词
PROTEIN-KINASE PKR; CONTROLS GENE-EXPRESSION; DOUBLE-STRANDED-RNA; INTERFERON-GAMMA; BINDING; RIBOSWITCHES; REGULATORS; BIOLOGY; DOMAIN;
D O I
10.1038/nchembio.234
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:896 / 903
页数:8
相关论文
共 33 条
[1]
Superantigen antagonist protects against lethal shock and defines a new domain for T-cell activation [J].
Arad, G ;
Levy, R ;
Hillman, D ;
Kaempfer, R .
NATURE MEDICINE, 2000, 6 (04) :414-421
[2]
Structure of a natural guanine-responsive riboswitch complexed with the metabolite hypoxanthine [J].
Batey, RT ;
Gilbert, SD ;
Montange, RK .
NATURE, 2004, 432 (7015) :411-415
[3]
Human interferon-γ mRNA autoregulates its translation through a pseudoknot that activates the interferon-inducible protein kinase PKR [J].
Ben-Asouli, Y ;
Banai, Y ;
Pel-Or, Y ;
Shir, A ;
Kaempfer, R .
CELL, 2002, 108 (02) :221-232
[4]
Minor-groove recognition of double-stranded RNA by the double-stranded RNA-binding domain from the RNA-activated protein kinase PKR [J].
Bevilacqua, PC ;
Cech, TR .
BIOCHEMISTRY, 1996, 35 (31) :9983-9994
[5]
Billiau A, 1996, ADV IMMUNOL, V62, P61, DOI 10.1016/S0065-2776(08)60428-9
[6]
Control of alternative RNA splicing and gene expression by eukaryotic riboswitches [J].
Cheah, Ming T. ;
Wachter, Andreas ;
Sudarsan, Narasimhan ;
Breaker, Ronald R. .
NATURE, 2007, 447 (7143) :497-U7
[7]
Circle DA, 1997, RNA, V3, P438
[8]
Dever T.E., 2007, TRANSLATIONAL CONTRO, P319
[9]
Impact of protein kinase PKR in cell biology:: from antiviral to antiproliferative action [J].
Garcia, M. A. ;
Gil, J. ;
Ventoso, I. ;
Guerra, S. ;
Domingo, E. ;
Rivas, C. ;
Esteban, M. .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2006, 70 (04) :1032-+
[10]
Hyperinducible expression of the interferon-gamma (IFN-gamma) gene and its suppression in systemic lupus erythematosus (SLE) [J].
Gerez, L ;
Shkolnik, T ;
Hirschmann, O ;
Lorber, M ;
Arad, G ;
Kaempfer, R .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 109 (02) :296-303