Zhang L, Pagano J S
Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill 27599-7295, USA.
Mol Cell Biol. 1997 Oct;17(10):5748-57. doi: 10.1128/MCB.17.10.5748.
The Epstein-Barr virus (EBV) BamHI Q promoter (Qp) is the only promoter used for the transcription of Epstein-Barr virus nuclear antigen 1 (EBNA-1) mRNA in cells in the most restricted (type I) latent infection state. However, Qp is inactive in type III latency. With the use of the yeast one-hybrid system, a new cellular gene has been identified that encodes proteins which bind to sequence in Qp. The deduced amino acid sequence of the gene has significant homology to the interferon regulatory factors (IRFs). This new gene and products including two splicing variants are designated IRF-7A, IRF-7B, and IRF-7C. The expression of IRF-7 is predominantly in spleen, thymus, and peripheral blood leukocytes (PBL). IRF-7 proteins were identified in primary PBL with specific antiserum against IRF-7B protein. IRF-7s can bind to interferon-stimulated response element (ISRE) sequence and repress transcriptional activation by both interferon and IRF-1. Additionally, a functional viral ISRE sequence, 5'-GCGAAAACGAAAGT-3', has been identified in Qp. Finally, the expression of IRF-7 is consistently high in type III latency cells and almost undetectable in type I latency, corresponding to the activity of endogenous Qp in these latency states and the ability of the IRF-7 proteins to repress Qp-reporter constructs. The identification of a functional viral ISRE and association of IRF-7 with type III latency may be relevant to the mechanism of regulation of Qp.
爱泼斯坦-巴尔病毒(EBV)的BamHI Q启动子(Qp)是在最严格的(I型)潜伏感染状态下,细胞中用于转录爱泼斯坦-巴尔病毒核抗原1(EBNA-1)mRNA的唯一启动子。然而,Qp在III型潜伏状态下无活性。利用酵母单杂交系统,已鉴定出一个新的细胞基因,该基因编码与Qp序列结合的蛋白质。该基因推导的氨基酸序列与干扰素调节因子(IRF)具有显著同源性。这个新基因及其包括两个剪接变体的产物被命名为IRF-7A、IRF-7B和IRF-7C。IRF-7主要在脾脏、胸腺和外周血白细胞(PBL)中表达。用针对IRF-7B蛋白的特异性抗血清在原代PBL中鉴定出IRF-7蛋白。IRF-7可以结合干扰素刺激反应元件(ISRE)序列,并抑制干扰素和IRF-1的转录激活。此外,在Qp中已鉴定出一个功能性病毒ISRE序列,5'-GCGAAAACGAAAGT-3'。最后,IRF-7在III型潜伏细胞中的表达始终很高,而在I型潜伏中几乎检测不到,这与这些潜伏状态下内源性Qp的活性以及IRF-7蛋白抑制Qp报告基因构建体的能力相对应。功能性病毒ISRE的鉴定以及IRF-7与III型潜伏的关联可能与Qp的调控机制有关。