The Nucleotides on the Stem-Loop RNA Structure in the Junction Region of the Hepatitis E Virus Genome Are Critical for Virus Replication

被引:56
作者
Cao, Dianjun [1 ]
Huang, Yao-Wei [1 ]
Meng, Xiang-Jin [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Coll Vet Med, Dept Biomed Sci & Pathobiol, Ctr Mol Med & Infect Dis, Blacksburg, VA 24061 USA
基金
美国国家卫生研究院;
关键词
LOCKED NUCLEIC-ACIDS; CIS-REACTIVE ELEMENT; ORF3; PROTEIN; GENE-EXPRESSION; CDNA-CLONES; IN-VITRO; CELLS; SWINE; INFECTION; TRANSLATION;
D O I
10.1128/JVI.01475-10
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
The roles of conserved nucleotides on the stem-loop (SL) structure in the intergenic region of the hepatitis E virus (HEV) genome in virus replication were determined by using Huh7 cells transfected with HEV SL mutant replicons containing reporter genes. One or two nucleotide mutations of the AGA motif on the loop significantly reduced HEV replication, and three or more nucleotide mutations on the loop abolished HEV replication. Mutations on the stem and of the subgenome start sequence also significantly inhibited HEV replication. The results indicated that both the sequence and the SL structure in the junction region play important roles in HEV replication.
引用
收藏
页码:13040 / 13044
页数:5
相关论文
共 44 条
[1]
AIKAWA TM, 2002, J GEN VIROL 7, V186, P1536
[2]
Human and swine hepatitis E viruses from Western India belong to different genotypes [J].
Arankalle, VA ;
Chobe, LP ;
Joshi, MV ;
Chadha, MS ;
Kundu, B ;
Walimbe, AM .
JOURNAL OF HEPATOLOGY, 2002, 36 (03) :417-425
[3]
Phylogenetic analysis of hepatitis E virus isolates from India (1976-1993) [J].
Arankalle, VA ;
Paranjape, S ;
Emerson, SU ;
Purcell, RH ;
Walimbe, AM .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1691-1700
[4]
Antisense inhibition of gene expression in cells by oligonucleotides incorporating locked nucleic acids: effect of mRNA target sequence and chimera design [J].
Braasch, DA ;
Liu, YH ;
Corey, DR .
NUCLEIC ACIDS RESEARCH, 2002, 30 (23) :5160-5167
[5]
Locked nucleic acid (LNA): fine-tuning the recognition of DNA and RNA [J].
Braasch, DA ;
Corey, DR .
CHEMISTRY & BIOLOGY, 2001, 8 (01) :1-7
[6]
Molecular biology and pathogenesis of hepatitis E virus [J].
Chandra, Vivek ;
Taneja, Shikha ;
Kalia, Manjula ;
Jameel, Shahid .
JOURNAL OF BIOSCIENCES, 2008, 33 (04) :451-464
[7]
The ORF3 Protein of Hepatitis E Virus Delays Degradation of Activated Growth Factor Receptors by Interacting with CIN85 and Blocking Formation of the Cbl-CIN85 Complex [J].
Chandra, Vivek ;
Kalia, Manjula ;
Hajela, Krishnan ;
Jameel, Shahid .
JOURNAL OF VIROLOGY, 2010, 84 (08) :3857-3867
[8]
FINE MAPPING OF A MOUSE METALLOTHIONEIN GENE METAL RESPONSE ELEMENT [J].
CULOTTA, VC ;
HAMER, DH .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) :1376-1380
[9]
In vitro replication of hepatitis E virus (HEV) genomes and of an HEV replicon expressing green fluorescent protein [J].
Emerson, SU ;
Nguyen, H ;
Graff, J ;
Stephany, DA ;
Brockington, A ;
Purcell, RH .
JOURNAL OF VIROLOGY, 2004, 78 (09) :4838-4846
[10]
Recombinant hepatitis E virus genomes infectious for primates: Importance of capping and discovery of a cis-reactive element [J].
Emerson, SU ;
Zhang, M ;
Meng, XJ ;
Nguyen, H ;
St Claire, M ;
Govindarajan, S ;
Huang, YK ;
Purcell, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (26) :15270-15275