Liu M, Kumar K U, Pater M M, Pater A
Basic Medical Sciences, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Canada.
Virus Res. 1998 Nov;58(1-2):73-82. doi: 10.1016/s0168-1702(98)00108-7.
The JC virus (JCV) control region contains AGGGAAGGGA, the tandem pentanucleotide repeat element (Pnt2). Several proteins specifically interacted via Pnt2 to regulate the expression of JCV early promoter-enhancer (JCV(E)) or late promoter-enhancer (JCV(L)). In this study, a JCV Pnt2 oligonucleotide probe was used to screen a cDNA expression library from glial P19 mouse embryonal carcinoma cells. A cDNA clone was isolated by Southwestern blot assay and it produced a protein that reproducibly and specifically bound to Pnt2. This cDNA had 100% homology to one of three previously identified mouse cDNAs called cellular nucleic acid binding proteins (Cnbps). Cnbps are a highly homologous family of eukaryotic genes implicated in functional interactions with cytoplasmic RNA and regulatory DNA elements. An mRNA of 2.2 kb of Pnt2-interacting Cnbp (PCnbp) was seen in undifferentiated, muscle or glial P19 cells. When expressed from a cDNA expression vector as a fusion protein that also contained 115 kDa from beta-galactosidase, a Pnt2 binding protein (PCNBP) specifically bound to Pnt2 in Southwestern blots as a 30 kDa component of the 145 kDa fusion protein. Furthermore, JCV(E) expression was negatively regulated by PCnbp produced in vivo from the cDNA expression vector. Regulation of JCV(L) was unaffected. We suggest a novel role for CNBP as a PCNBP that interacts with Pnt2 in the negative transcriptional regulation of JCV(E).
JC病毒(JCV)控制区包含AGGGAAGGGA,即串联五核苷酸重复元件(Pnt2)。几种蛋白质通过Pnt2特异性相互作用,以调节JCV早期启动子-增强子(JCV(E))或晚期启动子-增强子(JCV(L))的表达。在本研究中,使用JCV Pnt2寡核苷酸探针筛选来自神经胶质P19小鼠胚胎癌细胞的cDNA表达文库。通过蛋白质印迹法分离出一个cDNA克隆,它产生的一种蛋白质可重复性且特异性地与Pnt2结合。该cDNA与先前鉴定的三种小鼠cDNA之一具有100%的同源性,这三种cDNA被称为细胞核酸结合蛋白(Cnbps)。Cnbps是一个高度同源的真核基因家族,与细胞质RNA和调控DNA元件的功能相互作用有关。在未分化的、肌肉或神经胶质P19细胞中可观察到与Pnt2相互作用的Cnbp(PCnbp)的2.2 kb mRNA。当从cDNA表达载体表达为融合蛋白时,该融合蛋白还包含来自β-半乳糖苷酶的115 kDa,在蛋白质印迹中,一种Pnt2结合蛋白(PCNBP)作为145 kDa融合蛋白的30 kDa组分特异性地与Pnt2结合。此外,cDNA表达载体在体内产生的PCnbp对JCV(E)的表达具有负调控作用。JCV(L)的调控不受影响。我们认为CNBP作为PCNBP在JCV(E)的负转录调控中与Pnt2相互作用具有新的作用。