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T 细胞激活核因子对 BK 病毒的转录调控。

Transcriptional regulation of BK virus by nuclear factor of activated T cells.

机构信息

Graduate Program in Pathobiology, Brown University, Providence, Rhode Island 02912, USA.

出版信息

J Virol. 2010 Feb;84(4):1722-30. doi: 10.1128/JVI.01918-09. Epub 2009 Dec 2.

Abstract

The human polyomavirus BK virus (BKV) is a common virus for which 80 to 90% of the adult population is seropositive. BKV reactivation in immunosuppressed patients or renal transplant patients is the primary cause of polyomavirus-associated nephropathy (PVN). Using the Dunlop strain of BKV, we found that nuclear factor of activated T cells (NFAT) plays an important regulatory role in BKV infection. Luciferase reporter assays and chromatin immunoprecipitation assays demonstrated that NFAT4 bound to the viral promoter and regulated viral transcription and infection. The mutational analysis of the NFAT binding sites demonstrated complex functional interactions between NFAT, c-fos, c-jun, and the p65 subunit of NF-kappaB that together influence promoter activity and viral growth. These data indicate that NFAT is required for BKV infection and is involved in a complex regulatory network that both positively and negatively influences promoter activity and viral infection.

摘要

人类多瘤病毒 BK 病毒(BKV)是一种常见病毒,80%至 90%的成年人口血清呈阳性。免疫抑制患者或肾移植患者的 BKV 激活是导致多瘤病毒相关性肾病(PVN)的主要原因。使用 Dunlop 株 BKV,我们发现活化 T 细胞核因子(NFAT)在 BKV 感染中发挥重要的调节作用。荧光素酶报告基因检测和染色质免疫沉淀检测表明,NFAT4 结合到病毒启动子并调节病毒转录和感染。NFAT 结合位点的突变分析表明,NFAT、c-fos、c-jun 和 NF-κB 的 p65 亚基之间存在复杂的功能相互作用,共同影响启动子活性和病毒生长。这些数据表明 NFAT 是 BKV 感染所必需的,并且参与了一个复杂的调节网络,该网络对启动子活性和病毒感染具有正反两方面的影响。

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