Translational control of the picornavirus phenotype

被引:8
作者
Agol, VI [1 ]
机构
[1] Russian Acad Med Sci, Chumakov Inst Poliomyelitis & Virus Encephalites, Moscow, Russia
[2] Moscow MV Lomonosov State Univ, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
viruses; virulence; translation factors; differentiation; RNA-binding proteins;
D O I
10.1023/A:1010531228348
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
Picornaviruses are small animal viruses with positive-strand genomic RNA, which is translated using cap-independent internal translation initiation. The key role in this is played by cis elements of the 5 ' -untranslated region (5 ' -UTR) and, in particular, by the internal ribosome entry site (IRES). The function of translational cis elements requires both canonical translation initiation factors (eIFs) and additional IRES transacting factors (ITAFs). All known ITAFs are cell RNA-binding proteins which play a variety of functions in noninfected cells. Specific features of translational cis elements substantially affect the phenotype and, in particular, tissue tropism and pathogenic properties of picornaviruses. It is clear that, in some cases, the molecular mechanism involved is a change in interactions between viral cis elements and ITAFs. The properties and tissue distribution of ITAFs may determine the biological properties of other viruses that also use the IRES-dependent translation initiation. Since this mechanism is also involved in translation of several cell mRNAs, ITAF may contribute to the regulation of the most important aspects of the living activity in noninfected cells.
引用
收藏
页码:591 / 599
页数:9
相关论文
共 175 条
[1]   Modification of translational control elements as a new approach to design of attenuated picornavirus strains [J].
Agol, VI ;
Pilipenko, EV ;
Slobodskaya, OR .
JOURNAL OF BIOTECHNOLOGY, 1996, 44 (1-3) :119-128
[2]   RESTRICTED GROWTH OF ATTENUATED POLIOVIRUS STRAINS IN CULTURED-CELLS OF A HUMAN NEURO-BLASTOMA [J].
AGOL, VI ;
DROZDOV, SG ;
IVANNIKOVA, TA ;
KOLESNIKOVA, MS ;
KOROLEV, MB ;
TOLSKAYA, EA .
JOURNAL OF VIROLOGY, 1989, 63 (09) :4034-4038
[3]  
AGOL VI, 1991, MOL BIOL+, V25, P469
[4]  
AGOL VI, 1991, ADV VIRUS RES, V40, P103
[5]   Regulation of vascular endothelial growth factor (VEGF) expression is mediated by internal initiation of translation and alternative initiation of transcription [J].
Akiri, G ;
Nahari, D ;
Finkelstein, Y ;
Le, SY ;
Elroy-Stein, O ;
Levi, BZ .
ONCOGENE, 1998, 17 (02) :227-236
[6]   POLIOVIRUSES CONTAINING PICORNAVIRUS TYPE-1 AND/OR TYPE-2 INTERNAL RIBOSOMAL ENTRY SITE ELEMENTS - GENETIC HYBRIDS AND THE EXPRESSION OF A FOREIGN GENE [J].
ALEXANDER, L ;
LU, HH ;
WIMMER, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1406-1410
[7]  
Ali N, 2000, J BIOL CHEM, V275, P27531
[8]   The La antigen binds 5' noncoding region of the hepatitis C virus RNA in the context of the initiator AUG codon and stimulates internal ribosome entry site-mediated translation [J].
Ali, N ;
Siddiqui, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2249-2254
[9]   Demonstration of functional requirement of polypyrimidine tract-binding protein by SELEX RNA during hepatitis C virus internal ribosome entry site-mediated translation initiation [J].
Anwar, A ;
Ali, N ;
Tanveer, R ;
Siddiqui, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (44) :34231-34235
[10]   STRUCTURE OF THE FMDV TRANSLATION INITIATION SITE AND OF THE STRUCTURAL PROTEINS [J].
BECK, E ;
FORSS, S ;
STREBEL, K ;
CATTANEO, R ;
FEIL, G .
NUCLEIC ACIDS RESEARCH, 1983, 11 (22) :7873-7885