Cell-type specific regulation of gene expression by simian virus 40 T antigens

被引:28
作者
Cantalupo, Paul G. [1 ]
Saenz-Robles, Maria Teresa [1 ]
Rathi, Abhilasha V. [1 ]
Beerman, Rebecca W. [1 ]
Patterson, William H. [2 ]
Whitehead, Robert H. [2 ]
Pipas, James M. [1 ]
机构
[1] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA
[2] Vanderbilt Univ, Vanderbilt Digest Dis Res Ctr, Nashville, TN 37232 USA
关键词
SV40; Transformation; Gene expression; SMALL TUMOR-ANTIGEN; POLYMERASE-III TRANSCRIPTION; MULTIPLE COMPONENTS; EMBRYO FIBROBLASTS; QUIESCENT CELLS; SV40; RNA; TRANSFORMATION; ACTIVATION; BINDING;
D O I
10.1016/j.virol.2008.12.038
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
SV40 transforms cells through the action of two oncoproteins, large T antigen and small t antigen. Small t antigen targets phosphatase PP2A, while large T antigen stimulates cell proliferation and survival by action on multiple proteins, including the tumor suppressors Rb and p53. Large T antigen also binds components of the transcription initiation complex and several transcription factors. We examined global gene expression in SV40-transformed mouse embryo fibroblasts, and in enterocytes obtained from transgenic mice. SV40 transformation alters the expression of approximately 800 cellular genes in both systems. Much of this regulation is observed in both MEFs and enterocytes and is consistent with T antigen action on the Rb-E2F pathway. However, the regulation of many genes is cell-type specific, suggesting that unique signaling pathways are activated in different cell types upon transformation, and that the consequences of SV40 transformation depends on the type of cell targeted. (c) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:183 / 191
页数:9
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