Control of translation by the 5′- and 3′-terminal regions of the dengue virus genome

被引:92
作者
Chiu, WW
Kinney, RM
Dreher, TW
机构
[1] Oregon State Univ, Dept Microbiol, Corvallis, OR 97331 USA
[2] Oregon State Univ, Ctr Gene Res & Biotechnol, Corvallis, OR 97331 USA
[3] US Dept HHS, Ctr Dis Control & Prevent, Publ Hlth Serv, Div Vector Borne Infect Dis,Natl Ctr Infect Dis, Ft Collins, CO 80522 USA
关键词
D O I
10.1128/JVI.79.13.8303-8315.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genomic RNAs of flaviviruses such as dengue virus (DEN) have a 5' m(7)GpppN cap like those of cellular mRNAs but lack a 3' poly(A) tail. We have studied the contributions to translational expression of 5% and 3'-terminal regions of the DEN serotype 2 genome by using luciferase reporter mRNAs transfected into Vero cells. DCLD RNA contained the entire DEN 5' and 3' untranslated regions (UTRs), as well as the first 36 codons of the capsid coding region fused to the luciferase reporter gene. Capped DCLD RNA was as efficiently translated in Vero cells as capped GLGpA RNA, a reporter with UTRs from the highly expressed alpha-globin mRNA and a 72-residue poly(A) tail. Analogous reporter RNAs with regulatory sequences from West Nile and Sindbis viruses were also strongly expressed. Although capped DCLD RNA was expressed much more efficiently than its uncapped form, uncapped DCLD RNA was translated 6 to 12 times more efficiently than uncapped RNAs with UTRs from globin mRNA. The 5' cap and DEN 3' UTR were the main sources of the translational efficiency of DCLD RNA, and they acted synergistically in enhancing translation. The DEN 3' UTR increased mRNA stability, although this effect was considerably weaker than the enhancement of translational efficiency. The DEN 3' UTR thus has translational regulatory properties similar to those of a poly(A) tail. Its translation-enhancing effect was observed for RNAs with globin or DEN 5' sequences, indicating no codependency between viral 5' and 3' sequences. Deletion studies showed that translational enhancement provided by the DEN 3' UTR is attributable to the cumulative contributions of several conserved elements, as well as a nonconserved domain adjacent to the stop codon. One of the conserved elements was the conserved sequence (CS) CSI that is complementary to cCS1 present in the 5' end of the DEN polyprotein open reading frame. Complementarity between CS1 and cCS1 was not required for efficient translation.
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页码:8303 / 8315
页数:13
相关论文
共 52 条
[1]   Noncytopathic Sindbis virus RNA vectors for heterologous gene expression [J].
Agapov, EV ;
Frolov, I ;
Lindenbach, BD ;
Pragai, BM ;
Schlesinger, S ;
Rice, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :12989-12994
[2]  
[Anonymous], FIELDS VIROLOGY
[3]   Structures of immature flavivirus particles [J].
Zhang, Y ;
Corver, J ;
Chipman, PR ;
Zhang, W ;
Pletnev, SV ;
Sedlak, D ;
Baker, TS ;
Strauss, JH ;
Kuhn, RJ ;
Rossmann, MG .
EMBO JOURNAL, 2003, 22 (11) :2604-2613
[4]   THE 3'-NUCLEOTIDES OF FLAVIVIRUS GENOMIC RNA FORM A CONSERVED SECONDARY STRUCTURE [J].
BRINTON, MA ;
FERNANDEZ, AV ;
DISPOTO, JH .
VIROLOGY, 1986, 153 (01) :113-121
[5]   SEQUENCE AND SECONDARY STRUCTURE-ANALYSIS OF THE 5'-TERMINAL REGION OF FLAVIVIRUS GENOME RNA [J].
BRINTON, MA ;
DISPOTO, JH .
VIROLOGY, 1988, 162 (02) :290-299
[6]   A four-nucleotide translation enhancer in the 3′-terminal consensus sequence of the nonpolyadenylated mRNAs of rotavirus [J].
Chizhikov, V ;
Patton, JT .
RNA, 2000, 6 (06) :814-825
[7]   Fine mapping of a cis-acting sequence element in yellow fever virus RNA that is required for RNA replication and cyclization [J].
Corver, J ;
Lenches, E ;
Smith, K ;
Robison, RA ;
Sando, T ;
Strauss, EG ;
Strauss, JH .
JOURNAL OF VIROLOGY, 2003, 77 (03) :2265-2270
[8]   Translation of Sindbis virus mRNA: Analysis of sequences downstream of the initiating AUG codon that enhance translation [J].
Frolov, I ;
Schlesinger, S .
JOURNAL OF VIROLOGY, 1996, 70 (02) :1182-1190
[9]   Translational control of viral gene expression in eukaryotes [J].
Gale, M ;
Tan, SL ;
Katze, MG .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2000, 64 (02) :239-+
[10]   RNA PSEUDOKNOT DOMAIN OF TOBACCO MOSAIC-VIRUS CAN FUNCTIONALLY SUBSTITUTE FOR A POLY(A) TAIL IN PLANT AND ANIMAL-CELLS [J].
GALLIE, DR ;
WALBOT, V .
GENES & DEVELOPMENT, 1990, 4 (07) :1149-1157