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本文引用的文献

1
Insulators are fundamental components of the eukaryotic genomes.绝缘子是真核生物基因组的基本组成部分。
Heredity (Edinb). 2005 Jun;94(6):571-6. doi: 10.1038/sj.hdy.6800669.
2
The homeodomain protein CDP regulates mammary-specific gene transcription and tumorigenesis.同源结构域蛋白CDP调节乳腺特异性基因转录和肿瘤发生。
Mol Cell Biol. 2004 Jun;24(11):4810-23. doi: 10.1128/MCB.24.11.4810-4823.2004.
3
Rorgamma (Rorc) is a common integration site in type B leukemogenic virus-induced T-cell lymphomas.Rorgamma(Rorc)是B型致白血病病毒诱导的T细胞淋巴瘤中的常见整合位点。
J Virol. 2004 May;78(9):4943-6. doi: 10.1128/jvi.78.9.4943-4946.2004.
4
The type B leukemogenic virus truncated superantigen is dispensable for T-cell lymphomagenesis.B型白血病病毒截短超抗原对于T细胞淋巴瘤的发生并非必需。
J Virol. 2003 Mar;77(6):3866-70. doi: 10.1128/jvi.77.6.3866-3870.2003.
5
Unique resistance of I/LnJ mice to a retrovirus is due to sustained interferon gamma-dependent production of virus-neutralizing antibodies.I/LnJ小鼠对逆转录病毒的独特抗性归因于病毒中和抗体的持续产生,该产生依赖于γ干扰素。
J Exp Med. 2003 Jan 20;197(2):233-43. doi: 10.1084/jem.20021499.
6
Selection for c-myc integration sites in polyclonal T-cell lymphomas.多克隆T细胞淋巴瘤中c-myc整合位点的选择
J Virol. 2002 Mar;76(5):2087-99. doi: 10.1128/jvi.76.5.2087-2099.2002.
7
Type B leukemogenic virus has a T-cell-specific enhancer that binds AML-1.B型白血病病毒具有一个与AML-1结合的T细胞特异性增强子。
J Virol. 2001 Mar;75(5):2174-84. doi: 10.1128/JVI.75.5.2174-2184.2001.
8
C3H mouse mammary tumor virus superantigen function requires a splice donor site in the envelope gene.C3H小鼠乳腺肿瘤病毒超抗原功能需要包膜基因中的一个剪接供体位点。
J Virol. 2000 Oct;74(20):9431-40. doi: 10.1128/jvi.74.20.9431-9440.2000.
9
CDP is a repressor of mouse mammary tumor virus expression in the mammary gland.CDP是小鼠乳腺肿瘤病毒在乳腺中表达的一种阻遏物。
J Virol. 2000 Jul;74(14):6348-57. doi: 10.1128/jvi.74.14.6348-6357.2000.
10
The c-myc locus is a common integration site in type B retrovirus-induced T-cell lymphomas.c-myc基因座是B型逆转录病毒诱导的T细胞淋巴瘤中常见的整合位点。
J Virol. 2000 Mar;74(5):2466-71. doi: 10.1128/jvi.74.5.2466-2471.2000.

小鼠乳腺肿瘤病毒向致淋巴瘤病毒的转化。

Conversion of mouse mammary tumor virus to a lymphomagenic virus.

作者信息

Bhadra Sanchita, Lozano Mary M, Dudley Jaquelin P

机构信息

Section of Molecular Genetics and Microbiology, The University of Texas at Austin, Austin, TX 78712-0162, USA.

出版信息

J Virol. 2005 Oct;79(19):12592-6. doi: 10.1128/JVI.79.19.12592-12596.2005.

DOI:10.1128/JVI.79.19.12592-12596.2005
PMID:16160187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1211542/
Abstract

Type B leukemogenic virus is a variant of mouse mammary tumor virus (MMTV) that causes thymic lymphomas rather than mammary tumors in mice. We demonstrate that conversion of a mammotropic MMTV to a T-cell-tropic virus requires two alterations in the long terminal repeat: (i) acquisition of a T-cell-specific enhancer and (ii) loss of transcriptional repression through deletion of negative regulatory elements (NREs) or by suppression of NRE activity after appropriate positioning of the enhancer.

摘要

B型致白血病病毒是小鼠乳腺肿瘤病毒(MMTV)的一种变体,它在小鼠中引发胸腺淋巴瘤而非乳腺肿瘤。我们证明,嗜乳腺性MMTV向嗜T细胞病毒的转变需要长末端重复序列发生两处改变:(i)获得一个T细胞特异性增强子;(ii)通过缺失负调控元件(NRE)或在增强子适当定位后抑制NRE活性来消除转录抑制。