Polypyrimidine tract-binding protein influences negative strand RNA synthesis of dengue virus

被引:38
作者
Jiang, Linbin [1 ]
Yao, Huiling [2 ]
Duan, Xiaoqun [3 ]
Lu, Xi [1 ]
Liu, Yongming [1 ]
机构
[1] Guilin Med Univ, Inst Biotechnol, Guilin 541004, Guangxi, Peoples R China
[2] Guilin Normal Coll, Dept Phys, Guilin 541002, Guangxi, Peoples R China
[3] Guilin Med Univ, Dept Pharmacol, Guilin 541004, Guangxi, Peoples R China
关键词
Dengue virus; NS4A; PTB; RNA synthesis; YELLOW-FEVER VIRUS; RIBOSOME ENTRY SITE; NUCLEAR-LOCALIZATION; GENE-EXPRESSION; HCV REPLICATION; MESSENGER-RNA; TRANSLATION; NS1; PTB; REGION;
D O I
10.1016/j.bbrc.2009.05.036
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
Flavivirus non-structual protein 4A (NS4A) induces membrane rearrangements to form viral replication complex and functions as interferon antagonist. However, other non-structural roles of NS4A protein in relation to virus life-cycle are poorly defined. This study elucidated if dengue virus (DENV) NS4A protein interacts with host proteins and contributes to Viral pathogenesis by screening human liver cDNA yeast-two-hybrid library. Our study identified polypyrimidine tract-binding protein (PTB) as a novel interacting partner of DENV NS4A protein. We reported for the first time that PTB influenced DENV production. Gene-silencing studies showed that PTB did not have an effect on DENV entry and DENV RNA translation. Further functional studies revealed that PTB influenced DENV production by modulating negative strand RNA synthesis. This is the first study that enlightens the interaction of DENV NS4A protein with PTB. in addition to demonstrating the novel role of PTB in relation to mosquito-borne flavivirus life-cycle. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:187 / 192
页数:6
相关论文
共 40 条
[1]   Polypyrimidine-tract-binding protein is a component of the HCV RNA replication complex and necessary for RNA synthesis [J].
Aizaki, Hideki ;
Choi, Keum S. ;
Liu, Minyi ;
Li, Yi-jia ;
Lai, Michael M. C. .
JOURNAL OF BIOMEDICAL SCIENCE, 2006, 13 (04) :469-480
[2]   Vascular leakage in severe dengue virus infections: A potential role for the nonstructural viral protein NS1 and complement [J].
Avirutnan, P ;
Punyadee, N ;
Noisakran, S ;
Komoltri, C ;
Thiemmeca, S ;
Auethavornanan, K ;
Jairungsri, A ;
Kanlaya, R ;
Tangthawornchaikul, N ;
Puttikhunt, C ;
Pattanakitsakul, SN ;
Yenchitsomanus, PT ;
Mongkolsapaya, J ;
Kasinrerk, W ;
Sittisombut, N ;
Husmann, M ;
Blettner, M ;
Vasanawathana, S ;
Bhakdi, S ;
Malasit, P .
JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (08) :1078-1088
[3]   RNA-Protein interactions in regulation of picornavirus RNA translation [J].
Belsham, GJ ;
Sonenberg, N .
MICROBIOLOGICAL REVIEWS, 1996, 60 (03) :499-+
[4]   A polypyrimidine tract facilitates the expression of Kaposi's sarcoma-associated herpesvirus vFLIP through an internal ribosome entry site [J].
Bieleski, L ;
Hindley, C ;
Talbot, SJ .
JOURNAL OF GENERAL VIROLOGY, 2004, 85 :615-620
[5]   FLAVIVIRUS GENOME ORGANIZATION, EXPRESSION, AND REPLICATION [J].
CHAMBERS, TJ ;
HAHN, CS ;
GALLER, R ;
RICE, CM .
ANNUAL REVIEW OF MICROBIOLOGY, 1990, 44 :649-688
[6]   The polypyrimidine tract-binding protein (PTB) is required for efficient replication of hepatitis C virus (HCV) RNA [J].
Chang, KS ;
Luo, GX .
VIRUS RESEARCH, 2006, 115 (01) :1-8
[7]   Polypyrimidine-tract-binding protein affects transcription but not translation of mouse hepatitis virus RNA [J].
Choi, KS ;
Huang, PY ;
Lai, MMC .
VIROLOGY, 2002, 303 (01) :58-68
[8]   Interaction between the cellular protein eEF1A and the 3′-terminal stem-loop of West Nile virus genomic RNA facilitates viral minus-strand RNA synthesis [J].
Davis, William G. ;
Blackwell, Jerry L. ;
Shi, Pei-Yong ;
Brinton, Margo A. .
JOURNAL OF VIROLOGY, 2007, 81 (18) :10172-10187
[9]   Translation elongation factor-1α, La, and PTB interact with the 3′ untranslated region of dengue 4 virus RNA [J].
De Nova-Ocampo, M ;
Villegas-Sepúveda, N ;
del Angel, RM .
VIROLOGY, 2002, 295 (02) :337-347
[10]   Role of La autoantigen and polypyrimidine tract-binding protein in HCV replication [J].
Domitrovich, AM ;
Diebel, KW ;
Ali, N ;
Sarker, S ;
Siddiqui, A .
VIROLOGY, 2005, 335 (01) :72-86