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SV40 T抗原的氨基末端片段可转化REF52细胞。

An amino-terminal fragment of SV40 T antigen transforms REF52 cells.

作者信息

Sompayrac L, Danna K J

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80302.

出版信息

Virology. 1992 Nov;191(1):439-42. doi: 10.1016/0042-6822(92)90206-5.

DOI:10.1016/0042-6822(92)90206-5
PMID:1329329
Abstract

An SV40 mutant, T147D, encodes only the amino-terminal 147 amino acids of large T antigen and does not make small t antigen. We show here that a retrovirus which expresses this mutant T antigen transforms rat REF52 cells as efficiently as a retrovirus that expresses both the wild-type large and small T antigens. This cell line had previously been refractory to transformation by mutants that make short, amino-terminal fragments of T antigen.

摘要

一种SV40突变体T147D仅编码大T抗原的氨基末端147个氨基酸,不产生小t抗原。我们在此表明,表达这种突变T抗原的逆转录病毒转化大鼠REF52细胞的效率与表达野生型大T抗原和小t抗原的逆转录病毒相同。该细胞系以前对产生T抗原氨基末端短片段的突变体转化具有抗性。

相似文献

1
An amino-terminal fragment of SV40 T antigen transforms REF52 cells.SV40 T抗原的氨基末端片段可转化REF52细胞。
Virology. 1992 Nov;191(1):439-42. doi: 10.1016/0042-6822(92)90206-5.
2
The amino-terminal 147 amino acids of SV40 large T antigen transform secondary rat embryo fibroblasts.猴病毒40大T抗原的氨基末端147个氨基酸可转化大鼠胚胎次级成纤维细胞。
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3
Effects of mutations within the SV40 large T antigen ATPase/p53 binding domain on viral replication and transformation.猴空泡病毒40大T抗原ATP酶/p53结合域内突变对病毒复制和转化的影响。
Virus Genes. 1998;16(2):153-65. doi: 10.1023/a:1007941622680.
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Primary rat cells expressing a hybrid polyomavirus-simian virus 40 large T antigen have altered growth properties.表达杂交多瘤病毒-猿猴病毒40大T抗原的原代大鼠细胞具有改变的生长特性。
J Virol. 1993 Aug;67(8):4750-9. doi: 10.1128/JVI.67.8.4750-4759.1993.
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Binding of p53 and p105-RB is not sufficient for oncogenic transformation by a hybrid polyomavirus-simian virus 40 large T antigen.p53与p105-RB的结合不足以通过杂交多瘤病毒-猿猴病毒40大T抗原实现致癌转化。
J Virol. 1990 Nov;64(11):5250-9. doi: 10.1128/JVI.64.11.5250-5259.1990.
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A DNA replication-positive mutant of simian virus 40 that is defective for transformation and the production of infectious virions.一种猿猴病毒40的DNA复制阳性突变体,其在转化和产生传染性病毒粒子方面存在缺陷。
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An amino-terminal fragment of SV40 T antigen induces cellular DNA synthesis in quiescent rat cells.SV40 T抗原的氨基末端片段可诱导静止大鼠细胞中的细胞DNA合成。
Virology. 1994 May 1;200(2):849-53. doi: 10.1006/viro.1994.1255.
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Converting the JCV T antigen Rb binding domain to that of SV40 does not alter JCV's limited transforming activity but does eliminate viral viability.将多瘤病毒(JCV)T抗原的视网膜母细胞瘤(Rb)结合结构域转换为猴空泡病毒40(SV40)的该结构域,不会改变JCV有限的转化活性,但会消除病毒的生存能力。
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The cellular chromatin is an important target for SV40 large T antigen in maintaining the transformed phenotype.细胞染色质是猿猴病毒40大T抗原维持转化表型的重要靶点。
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10
A new SV40 mutant that encodes a small fragment of T antigen transforms established rat and mouse cells.一种编码T抗原小片段的新型SV40突变体可转化已建立的大鼠和小鼠细胞。
Virology. 1988 Apr;163(2):391-6. doi: 10.1016/0042-6822(88)90279-6.

引用本文的文献

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Removal of a small C-terminal region of JCV and SV40 large T antigens has differential effects on transformation.去除多瘤病毒(JCV)和猴病毒40(SV40)大T抗原的小C末端区域对转化有不同影响。
Virology. 2014 Nov;468-470:47-56. doi: 10.1016/j.virol.2014.07.038. Epub 2014 Aug 16.
2
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。
Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):3679-84. doi: 10.1073/pnas.94.8.3679.
3
The block of adipocyte differentiation by a C-terminally truncated, but not by full-length, simian virus 40 large tumor antigen is dependent on an intact retinoblastoma susceptibility protein family binding domain.
C末端截短而非全长的猿猴病毒40大T抗原对脂肪细胞分化的阻断依赖于完整的视网膜母细胞瘤易感蛋白家族结合结构域。
J Virol. 1996 Feb;70(2):745-52. doi: 10.1128/JVI.70.2.745-752.1996.
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J Virol. 1994 Feb;68(2):668-73. doi: 10.1128/JVI.68.2.668-673.1994.
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Independent expression of the transforming amino-terminal domain of SV40 large I antigen from an alternatively spliced third SV40 early mRNA.来自剪接变异的第三个SV40早期mRNA的SV40大T抗原转化性氨基末端结构域的独立表达。
EMBO J. 1993 Dec;12(12):4739-46. doi: 10.1002/j.1460-2075.1993.tb06162.x.
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