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Tmevpg1是控制泰勒氏病毒持续性的一个候选基因,可能参与γ干扰素的调节。

Tmevpg1, a candidate gene for the control of Theiler's virus persistence, could be implicated in the regulation of gamma interferon.

作者信息

Vigneau Soline, Rohrlich Pierre-Simon, Brahic Michel, Bureau Jean-François

机构信息

Unité des Virus Lents, CNRS URA 1930, Institut Pasteur, Paris, France.

出版信息

J Virol. 2003 May;77(10):5632-8. doi: 10.1128/jvi.77.10.5632-5638.2003.

Abstract

The Tmevp3 locus controls the load of Theiler's virus RNA during persistent infection of the mouse central nervous system (CNS). We identified a candidate gene at this locus, Tmevpg1, by using a positional cloning approach. Tmevpg1 and its human ortholog, TMEVPG1, are expressed in the immune system and encode what appears to be a noncoding RNA. They are located in a cluster of cytokine genes that includes the genes for gamma interferon and one or two homolog of interleukin-10. We now report that Tmevpg1 is expressed in CNS-infiltrating immune cells of resistant B10.S mice, but not in those of susceptible SJL/J mice, following inoculation with Theiler's virus. The pattern of expression of Tmevpg1 is the same in B10.S mice and in SJL/J mice congenic for the resistant B10.S haplotype of Tmevp3. Nineteen polymorphisms were identified when the Tmevpg1 genes of B10.S and SJL/J mice were compared. Interestingly, Tmevpg1 is down regulated after in vitro stimulation of murine CD4(+) or CD8(+) splenocytes, whereas Ifng is up regulated. Similar patterns of expression of TMEVPG1 and IFNG were observed in human NK cells and CD4(+) and CD8(+) T lymphocytes. Therefore, Tmevpg1 is a strong candidate gene for the Tmevp3 locus and may be involved in the control of Ifng gene expression.

摘要

Tmevp3基因座在小鼠中枢神经系统(CNS)持续感染期间控制泰勒氏病毒RNA的负荷。我们通过定位克隆方法在该基因座鉴定出一个候选基因Tmevpg1。Tmevpg1及其人类同源基因TMEVPG1在免疫系统中表达,并编码一种似乎是非编码RNA的物质。它们位于一组细胞因子基因簇中,该基因簇包括γ干扰素基因以及白细胞介素-10的一个或两个同源基因。我们现在报告,在用泰勒氏病毒接种后,Tmevpg1在抗性B10.S小鼠的CNS浸润免疫细胞中表达,但在易感SJL/J小鼠的此类细胞中不表达。Tmevpg1的表达模式在B10.S小鼠和具有Tmevp3抗性B10.S单倍型同基因的SJL/J小鼠中是相同的。比较B10.S和SJL/J小鼠的Tmevpg1基因时,鉴定出19个多态性。有趣的是,体外刺激小鼠CD4(+)或CD8(+)脾细胞后,Tmevpg1表达下调,而Ifng表达上调。在人类NK细胞以及CD4(+)和CD8(+) T淋巴细胞中观察到TMEVPG1和IFNG的类似表达模式。因此,Tmevpg1是Tmevp3基因座的一个强有力候选基因,并可能参与Ifng基因表达的调控。

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