Herpesvirus saimiri ORF57: a post-transcriptional regulatory protein

被引:35
作者
Boyne, James R. [1 ]
Colgan, Kevin J. [1 ]
Whitehouse, Adrian [1 ,2 ]
机构
[1] Univ Leeds, Inst Mol & Cellular Biol, Fac Biol Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
基金
英国惠康基金;
关键词
Herpesvirus saimiri; mRNA processing; ORF57; review;
D O I
10.2741/2898
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
Herpesvirus saimiri (HVS) is the prototype gamma-2 herpesvirus and is a useful model to study the basic mechanisms of lytic replication in this herpesvirus subfamily. This review focuses upon the role of an essential lytic protein, ORF57, which is functionally conserved in all classes of herpesviruses. ORF57 is a multidomain, multifunctional protein responsible for both activation and repression of viral gene expression at a post-transcriptional level. ORF57-mediated repression of gene expression is determined by mRNA processing signals, in particular the presence of an intron within the target gene. This may also be linked to the ability of ORF57 to redistribute SC-35 and U2 splicing factors into specific nuclear domains. ORF57 also plays a pivotal role in transactivating viral gene expression by specifically mediating the nuclear export of HVS intronless transcripts. ORF57 has the ability to shuttle between the nucleus and the cytoplasm, bind viral RNA and recruit cellular nuclear export proteins, such as hTREX components and TAP, onto the viral mRNA. This enables the efficient nuclear export and cytoplasmic accumulation of virus intronless mRNA.
引用
收藏
页码:2928 / 2938
页数:11
相关论文
共 86 条
[61]   REF proteins mediate the export of spliced and unspliced mRNAs from the nucleus [J].
Rodrigues, JP ;
Rode, M ;
Gatfield, D ;
Blencowe, BJ ;
Carmo-Fonseca, M ;
Izaurralde, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (03) :1030-+
[62]   Nucleotide sequence of the Kaposi sarcoma-associated herpesvirus (HHV8) [J].
Russo, JJ ;
Bohenzky, RA ;
Chien, MC ;
Chen, J ;
Yan, M ;
Maddalena, D ;
Parry, JP ;
Peruzzi, D ;
Edelman, IS ;
Chang, Y ;
Moore, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14862-14867
[63]   The herpes simplex virus type 1 regulatory protein ICP27 coimmunoprecipitates with anti-sm antiserum, and the C terminus appears to be required for this interaction [J].
SandriGoldin, RM ;
Hibbard, MK .
JOURNAL OF VIROLOGY, 1996, 70 (01) :108-118
[64]   Functional proteomic analysis of human nucleolus [J].
Scherl, A ;
Couté, Y ;
Déon, C ;
Callé, A ;
Kindbeiter, K ;
Sanchez, JC ;
Greco, A ;
Hochstrasser, D ;
Diaz, JJ .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (11) :4100-4109
[65]   MUTANTS IN A YEAST RAN BINDING-PROTEIN ARE DEFECTIVE IN NUCLEAR TRANSPORT [J].
SCHLENSTEDT, G ;
WONG, DH ;
KOEPP, DM ;
SILVER, PA .
EMBO JOURNAL, 1995, 14 (21) :5367-5378
[66]   ICP27 interacts with SRPK1 to mediate HSV splicing inhibition by altering SR protein phosphorylation [J].
Sciabica, KS ;
Dai, QJ ;
Sandri-Goldin, RM .
EMBO JOURNAL, 2003, 22 (07) :1608-1619
[67]   Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)(+) RNA and nuclear pores [J].
Segref, A ;
Sharma, K ;
Doye, V ;
Hellwig, A ;
Huber, J ;
Luhrmann, R ;
Hurt, E .
EMBO JOURNAL, 1997, 16 (11) :3256-3271
[68]  
Shaw PJ, 1995, ANNU REV CELL DEV BI, V11, P93, DOI 10.1146/annurev.cb.11.110195.000521
[69]   Cse1p is involved in export of yeast importin α from the nucleus [J].
Solsbacher, J ;
Maurer, P ;
Bischoff, FR ;
Schlenstedt, G .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6805-6815
[70]   A viral gene that activates lytic cycle expression of Kaposi's sarcoma-associated herpesvirus [J].
Sun, R ;
Lin, SF ;
Gradoville, L ;
Yuan, Y ;
Zhu, FX ;
Miller, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10866-10871