TFIIH transcription factor, a target for the Rift Valley hemorrhagic fever virus

被引:244
作者
Le May, N
Dubaele, S
De Santis, LP
Billecocq, A
Bouloy, M
Egly, JM
机构
[1] Inst Pasteur, Unite Genet Mol Bunyavirides, F-75724 Paris 15, France
[2] CU Strasbourg, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
关键词
D O I
10.1016/S0092-8674(04)00132-1
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
The Rift Valley fever virus (RVFV) is the causative agent of fatal hemorrhagic fever in humans and acute hepatitis in ruminants. We found that infection by RVFV leads to a rapid and drastic suppression of host cellular RNA synthesis that parallels a decrease of the TFIIH transcription factor cellular concentration. Using yeast two hybrid system, recombinant technology, and confocal microscopy, we further demonstrated that the nonstructural viral NSs protein interacts with the p44 component of TFIIH to form nuclear filamentous structures that also contain XPB subunit of TFIIH. By competing with XPD, the natural partner of p44 within TFIIH, and sequestering p44 and XPB subunits, NSs prevents the assembly of TFIIH subunits, thus destabilizing the normal host cell life. These observations shed light on the mechanism utilized by RVFV to evade the host response.
引用
收藏
页码:541 / 550
页数:10
相关论文
共 45 条
[1]  
[Anonymous], 2000, Wkly Epidemiol Rec, V75, P370
[2]  
[Anonymous], 2000, Wkly Epidemiol Rec, V75, P392
[3]   EFFECT OF MENGOVIRUS INFECTION ON ACTIVITY OF DNA-DEPENDENT RNA POLYMERASE OF L-CELLS [J].
BALTIMORE, D ;
FRANKLIN, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (08) :1383-&
[4]  
BILLECOCQ A, 2003, 12 INT C NEG STRAND, P137
[5]  
BISHOP DH, 1996, BUNYAVIRIDAE
[6]   Genetic evidence for an interferon-antagonistic function of Rift Valley fever virus nonstructural protein NSs [J].
Bouloy, M ;
Janzen, C ;
Vialat, P ;
Khun, H ;
Pavlovic, J ;
Huerre, M ;
Haller, O .
JOURNAL OF VIROLOGY, 2001, 75 (03) :1371-1377
[7]   Bunyamwera bunyavirus nonstructural protein NSs is a nonessential gene product that contributes to viral pathogenesis [J].
Bridgen, A ;
Weber, F ;
Fazakerley, JK ;
Elliott, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :664-669
[8]   Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH [J].
Coin, F ;
Marinoni, JC ;
Rodolfo, C ;
Fribourg, S ;
Pedrini, AM ;
Egly, JM .
NATURE GENETICS, 1998, 20 (02) :184-188
[9]  
CONAWAY JW, 1989, J BIOL CHEM, V264, P2357
[10]   INHIBITION OF TRANSCRIPTION FACTOR ACTIVITY BY POLIOVIRUS [J].
CRAWFORD, N ;
FIRE, A ;
SAMUELS, M ;
SHARP, PA ;
BALTIMORE, D .
CELL, 1981, 27 (03) :555-561