A noncoding RNA produced by arthropod-borne flaviviruses inhibits the cellular exoribonuclease XRN1 and alters host mRNA stability

被引:159
作者
Moon, Stephanie L. [1 ]
Anderson, John R. [1 ]
Kumagai, Yutaro [2 ]
Wilusz, Carol J. [1 ]
Akira, Shizuo [2 ]
Khromykh, Alexander A. [3 ]
Wilusz, Jeffrey [1 ]
机构
[1] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
[2] Osaka Univ, Microbial Dis Res Inst, Immunol Frontier Res Ctr, Dept Host Def,Host Def Lab, Suita, Osaka 5650871, Japan
[3] Univ Queensland, Sch Chem & Mol Biosci, Australian Infect Dis Res Ctr, Brisbane, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
flavivirus; mRNA decay; mRNA stability; noncoding RNA; virus-host interaction; POLY(RC) BINDING-PROTEINS; GENE-EXPRESSION; SUBGENOMIC RNA; WEST-NILE; P-BODIES; DECAY; PSEUDOKNOT; CELLS; DEGRADATION; ELEMENTS;
D O I
10.1261/rna.034330.112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All arthropod-borne flaviviruses generate a short noncoding RNA (sfRNA) from the viral 3' untranslated region during infection due to stalling of the cellular 5'-to-3' exonuclease XRN1. We show here that formation of sfRNA also inhibits XRN1 activity. Cells infected with Dengue or Kunjin viruses accumulate uncapped mRNAs, decay intermediates normally targeted by XRN1. XRN1 repression also resulted in the increased overall stability of cellular mRNAs in flavivirus-infected cells. Importantly, a mutant Kunjin virus that cannot form sfRNA but replicates to normal levels failed to affect host mRNA stability or XRN1 activity. Expression of sfRNA in the absence of viral infection demonstrated that sfRNA formation was directly responsible for the stabilization of cellular mRNAs. Finally, numerous cellular mRNAs were differentially expressed in an sfRNA-dependent fashion in a Kunjin virus infection. We conclude that flaviviruses incapacitate XRN1 during infection and dysregulate host mRNA stability as a result of sfRNA formation.
引用
收藏
页码:2029 / 2040
页数:12
相关论文
共 47 条
[1]   Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility [J].
Astuti, Dewi ;
Morris, Mark R. ;
Cooper, Wendy N. ;
Staals, Raymond H. J. ;
Wake, Naomi C. ;
Fews, Graham A. ;
Gill, Harmeet ;
Gentle, Dean ;
Shuib, Salwati ;
Ricketts, Christopher J. ;
Cole, Trevor ;
van Essen, Anthonie J. ;
van Lingen, Richard A. ;
Neri, Giovanni ;
Opitz, John M. ;
Rump, Patrick ;
Stolte-Dijkstra, Irene ;
Mueller, Ferenc ;
Pruijn, Ger J. M. ;
Latif, Farida ;
Maher, Eamonn R. .
NATURE GENETICS, 2012, 44 (03) :277-U75
[2]   P bodies, stress granules, and viral life cycles [J].
Beckham, Carla J. ;
Parker, Roy .
CELL HOST & MICROBE, 2008, 3 (04) :206-212
[3]   Promoter Elements Regulate Cytoplasmic mRNA Decay [J].
Bregman, Almog ;
Avraham-Kelbert, Moran ;
Barkai, Oren ;
Duek, Lea ;
Guterman, Adi ;
Choder, Mordechai .
CELL, 2011, 147 (07) :1473-1483
[4]   Structural and biochemical studies of the 5′→3′ exoribonuclease Xrn1 [J].
Chang, Jeong Ho ;
Xiang, Song ;
Xiang, Kehui ;
Manley, James L. ;
Tong, Liang .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2011, 18 (03) :270-U49
[5]   Control of gene expression during T cell activation: alternate regulation of mRNA transcription and mRNA stability [J].
Cheadle, C ;
Fan, JS ;
Cho-Chung, YS ;
Werner, T ;
Ray, J ;
Do, L ;
Gorospe, M ;
Becker, KG .
BMC GENOMICS, 2005, 6 (1)
[6]   Mechanisms of deadenylation-dependent decay [J].
Chen, Chyi-Ying A. ;
Shyu, Ann-Bin .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2011, 2 (02) :167-183
[7]   Strategies for viral RNA stability: live long and prosper [J].
Dickson, Alexa M. ;
Wilusz, Jeffrey .
TRENDS IN GENETICS, 2011, 27 (07) :286-293
[8]   Poliovirus-Mediated Disruption of Cytoplasmic Processing Bodies [J].
Dougherty, Jonathan D. ;
White, James P. ;
Lloyd, Richard E. .
JOURNAL OF VIROLOGY, 2011, 85 (01) :64-75
[9]   Major role for mRNA stability in shaping the kinetics of gene induction [J].
Elkon, Ran ;
Zlotorynski, Eitan ;
Zeller, Karen I. ;
Agami, Reuven .
BMC GENOMICS, 2010, 11
[10]   Interaction of TIA-1/TIAR with West Nile and dengue virus products in infected cells interferes with stress granule formation and processing body assembly [J].
Emara, Mohamed M. ;
Brinton, Margo A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (21) :9041-9046