Polyomavirus T antigens: molecular chaperones for multiprotein complexes.
作者信息
Brodsky J L, Pipas J M
机构信息
Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
出版信息
J Virol. 1998 Jul;72(7):5329-34. doi: 10.1128/JVI.72.7.5329-5334.1998.
Abstract
摘要
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本文引用的文献
1
The J domain of simian virus 40 large T antigen is required to functionally inactivate RB family proteins.猴病毒40大T抗原的J结构域是功能性失活RB家族蛋白所必需的。
Mol Cell Biol. 1998 Mar;18(3):1408-15. doi: 10.1128/MCB.18.3.1408.
2
The DnaJ domain of polyomavirus large T antigen is required to regulate Rb family tumor suppressor function.多瘤病毒大T抗原的DnaJ结构域是调节Rb家族肿瘤抑制功能所必需的。
J Virol. 1997 Dec;71(12):9410-6. doi: 10.1128/JVI.71.12.9410-9416.1997.
3
Inactivation of pRB-related proteins p130 and p107 mediated by the J domain of simian virus 40 large T antigen.由猿猴病毒40大T抗原的J结构域介导的pRB相关蛋白p130和p107的失活。
Mol Cell Biol. 1997 Sep;17(9):4979-90. doi: 10.1128/MCB.17.9.4979.
4
The amino-terminal transforming region of simian virus 40 large T and small t antigens functions as a J domain.猴病毒40大T抗原和小t抗原的氨基末端转化区作为一个J结构域发挥作用。
Mol Cell Biol. 1997 Aug;17(8):4761-73. doi: 10.1128/MCB.17.8.4761.
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Tiny T antigen: an autonomous polyomavirus T antigen amino-terminal domain.微小T抗原：一种自主型多瘤病毒T抗原的氨基末端结构域。
J Virol. 1997 Aug;71(8):6068-74. doi: 10.1128/JVI.71.8.6068-6074.1997.
6
DnaJ/hsp40 chaperone domain of SV40 large T antigen promotes efficient viral DNA replication.猴空泡病毒40大T抗原的DnaJ/hsp40伴侣结构域促进高效的病毒DNA复制。
Genes Dev. 1997 May 1;11(9):1098-110. doi: 10.1101/gad.11.9.1098.
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The T/t common exon of simian virus 40, JC, and BK polyomavirus T antigens can functionally replace the J-domain of the Escherichia coli DnaJ molecular chaperone.猿猴病毒40、JC病毒和BK多瘤病毒T抗原的T/t共有外显子可在功能上替代大肠杆菌DnaJ分子伴侣的J结构域。
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8
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Genes Dev. 1997 Apr 1;11(7):815-23. doi: 10.1101/gad.11.7.815.
9
Adding an Rb-binding site to an N-terminally truncated simian virus 40 T antigen restores growth to high cell density, and the T common region in trans provides anchorage-independent growth and rapid growth in low serum concentrations.在N端截短的猿猴病毒40 T抗原上添加一个Rb结合位点可使细胞生长至高密度，并且反式作用的T共同区域可提供不依赖贴壁的生长以及在低血清浓度下的快速生长。
J Virol. 1997 Mar;71(3):1888-96. doi: 10.1128/JVI.71.3.1888-1896.1997.
10
DNA tumor viruses and Src family tyrosine kinases, an intimate relationship.
Virology. 1997 Jan 20;227(2):271-80. doi: 10.1006/viro.1996.8316.
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