The carboxyl-terminal domain of large T antigen rescues SV40 host range activity in trans independent of acetylation

被引:15
作者
Poulin, Danielle L.
DeCaprio, James A.
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
Simian virus 40; SV40; host range; large T Ag; replication;
D O I
10.1016/j.virol.2006.01.046
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The host range activity of SV40 has been described as the inability of mutant viruses with deletions in the C terminal region of large T Ag to replicate in certain types of African green monkey kidney cells. We constructed new mutant viruses expressing truncated T Ag proteins and found that these mutant viruses exhibited the host range phenotype. The host range phenotype was independent of acetylation of T Ag at lysine 697. Co-expression of the C terminal domain of T Ag (aa 627-708) in trans increased both T Ag and VP1 mRNA as well as protein levels for host range mutant viruses in the restrictive cell type. In addition, the T Ag 627-708 fragment promoted the productive lytic infection of host range mutant viruses in the nonpermissive cell type. The carboxyl-terminal region of T Ag contains a biological function essential for the SV40 viral life cycle. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:212 / 221
页数:10
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