Faculty Opinions recommendation of The vaccinia virus K1L gene product inhibits host NF-kappaB activation by preventing IkappaBalpha degradation.

Author(s):  
Grant McFadden
2002 ◽  
Vol 76 (19) ◽  
pp. 9773-9786 ◽  
Author(s):  
Laura Doglio ◽  
Ario De Marco ◽  
Sibylle Schleich ◽  
Norbert Roos ◽  
Jacomine Krijnse Locker

ABSTRACT Vaccinia virus (VV), a member of the poxvirus family, is unique among most other DNA viruses in that both transcription and DNA replication occur in the cytoplasm of the host cell. It was recently shown by electron microscopy (EM) that soon after viral DNA synthesis is initiated in HeLa cells, the replication sites become enwrapped by the membrane of the endoplasmic reticulum (ER). In the same study, a novel VV membrane protein, the E8R gene product, that may play a role in the ER wrapping process was identified (N. Tolonen, L. Doglio, S. Schleich, and J. Krijnse Locker, Mol. Biol. Cell 12:2031-2046, 2001). In the present study, the gene product of E8R was characterized both biochemically and morphologically. We show that E8R is made predominantly early in infection but is packaged into the virion. On two-dimensional gel electrophoresis, the protein appeared as a single spot throughout the VV life cycle; however, in the assembled virion, the protein underwent several modifications which resulted in a change in its molecular weight and its isoelectric point. EM of labeled cryosections of infected HeLa cells showed that the protein localized to the ER and to membranes located on one side of the Golgi complex as early as 1 h postinfection. Late in infection, E8R was additionally associated with membranes of immature virions and with intracellular mature viruses. Although E8R is predominantly associated with membranes, we show that the protein is associated with viral cores; the protein is present in cores made with NP-40-dithiothreitol as well as in incoming cores, the result of the viral entry process, early in infection. Finally, we show that E8R can be phosphorylated in vitro by the viral kinase F10L. It is able to bind DNA in vitro, and this binding may be modulated by phosphorylation by F10L. A putative role of the E8R gene product throughout the VV life cycle is discussed.


Virology ◽  
1995 ◽  
Vol 214 (1) ◽  
pp. 177-188 ◽  
Author(s):  
JANE E. PARKINSON ◽  
CHRISTOPHER M. SANDERSON ◽  
GEOFFREY L. SMITH

2002 ◽  
Vol 76 (17) ◽  
pp. 8973-8976 ◽  
Author(s):  
Chelsea M. Byrd ◽  
Tove' C. Bolken ◽  
Dennis E. Hruby

ABSTRACT Maturation of vaccinia virus (VV) core proteins is required for the production of infectious virions. The VV G1L and I7L gene products are the leading candidates for the viral core protein proteinase (vCPP). Using transient-expression assays, data were obtained to demonstrate that the I7L gene product and its encoded cysteine proteinase activity are responsible for vCPP activity.


Virology ◽  
2007 ◽  
Vol 367 (2) ◽  
pp. 398-412 ◽  
Author(s):  
Sayuri E.M. Kato ◽  
Richard C. Condit ◽  
Nissin Moussatché
Keyword(s):  

2003 ◽  
Vol 77 (10) ◽  
pp. 6014-6028 ◽  
Author(s):  
Sonja Welsch ◽  
Laura Doglio ◽  
Sibylle Schleich ◽  
Jacomine Krijnse Locker

ABSTRACT The vaccinia virus (VV) I3L gene product is a single-stranded DNA-binding protein made early in infection that localizes to the cytoplasmic sites of viral DNA replication (S. C. Rochester and P. Traktman, J. Virol. 72:2917-2926, 1998). Surprisingly, when replication was blocked, the protein localized to distinct cytoplasmic spots (A. Domi and G. Beaud, J. Gen. Virol. 81:1231-1235, 2000). Here these I3L-positive spots were characterized in more detail. By using an anti-I3L peptide antibody we confirmed that the protein localized to the cytoplasmic sites of viral DNA replication by both immunofluorescence and electron microscopy (EM). Before replication had started or when replication was inhibited with hydroxyurea or cytosine arabinoside, I3L localized to distinct cytoplasmic punctate structures of homogenous size. We show that these structures are not incoming cores or cytoplasmic sites of VV early mRNA accumulation. Instead, morphological and quantitative data indicate that they are specialized sites where the parental DNA accumulates after its release from incoming viral cores. By EM, these sites appeared as complex, electron-dense structures that were intimately associated with the cellular endoplasmic reticulum (ER). By double labeling of cryosections we show that they contain DNA and a viral early protein, the gene product of E8R. Since E8R is a membrane protein that is able to bind to DNA, the localization of this protein to the I3L puncta suggests that they are composed of membranes. The results are discussed in relation to our previous data showing that the process of viral DNA replication also occurs in close association with the ER.


Virology ◽  
1998 ◽  
Vol 250 (2) ◽  
pp. 302-315 ◽  
Author(s):  
T.V. Sharp ◽  
F. Moonan ◽  
A. Romashko ◽  
B. Joshi ◽  
G.N. Barber ◽  
...  

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