Ahn Byung Chul, Breitenbach Jonathan E, Kim Seong K, O'Callaghan Dennis J
Center for Molecular and Tumor Virology, Department of Microbiology and Immunology, Louisiana State University Health Sciences Center, 1501 Kings Highway, PO Box 33932, Shreveport, LA 71130-3932, USA.
Virology. 2007 Jun 20;363(1):15-25. doi: 10.1016/j.virol.2007.01.024. Epub 2007 Feb 15.
The unique IR3 gene of equine herpesvirus 1 (EHV-1) is expressed as a late 1.0-kb transcript. Previous studies confirmed the IR3 transcription initiation site and tentatively identified other cis-acting elements specific to IR3 such as a TATA box, a 443 base pair 5'untranslated region (UTR), a 285 base pair open reading frame (ORF), and a poly adenylation (A) signal [Holden, V.R., Harty, R.N., Yalamanchili, R.R., O'Callaghan, D.J., 1992. The IR3 gene of equine herpesvirus type 1: a unique gene regulated by sequences within the intron of the immediate-early gene. DNA Seq. 3, 143-152]. Transient transfection assays revealed that the IR3 promoter is strongly trans-activated by the IE protein (IEP) and that coexpression of the IEP with the early EICP0 and IR4 regulatory proteins results in maximal trans-activation of the IR3 promoter. Gel shift assays revealed that the IEP directly binds to the IR3 promoter region. Western blot analysis showed that the IR3 protein produced in E. coli was detected by antibodies to IR3 synthetic peptides; however, the IR3 protein was not detected in EHV-1 infected cell extracts by these same anti-IR3 antibodies, even though the IR3 transcript was detected by northern blot. These findings suggest that the IR3 may not be expressed to a protein. Expression of an IR3/GFP fusion gene was not observed, but expression of a GFP/IR3 fusion gene was detected by fluorescent microscopy. In further attempts to detect the IR3/GFP fusion protein using anti-GFP antibody, western blot analysis showed that the IR3/GFP fusion protein was not detected in vivo. Interestingly, a truncated form of the GFP/IR3 protein was synthesized from the GFP/IR3 fusion gene. However, GFP/IR3 and IR3/GFP fusion proteins of the predicted sizes were synthesized by in vitro coupled transcription and translation of the fusion genes, suggesting poor expression of the IR3 protein in vivo. The possible role of the IR3 transcript in EHV-1 infection is discussed.
马疱疹病毒1型(EHV-1)独特的IR3基因表达为一种晚期1.0 kb转录本。先前的研究证实了IR3转录起始位点,并初步鉴定了IR3特有的其他顺式作用元件,如TATA盒、一个443个碱基对的5'非翻译区(UTR)、一个285个碱基对的开放阅读框(ORF)和一个聚腺苷酸化(A)信号[霍尔登,V.R.,哈蒂,R.N.,亚拉曼奇利,R.R.,奥卡拉汉,D.J.,1992。马疱疹病毒1型的IR3基因:一个由立即早期基因内含子内序列调控的独特基因。DNA序列。3,143 - 152]。瞬时转染试验表明,IR3启动子被立即早期蛋白(IEP)强烈反式激活,并且IEP与早期EICP0和IR4调控蛋白的共表达导致IR3启动子的最大反式激活。凝胶迁移试验表明,IEP直接结合到IR3启动子区域。蛋白质印迹分析表明,用针对IR3合成肽的抗体可检测到大肠杆菌中产生的IR3蛋白;然而,即使通过Northern印迹检测到了IR3转录本,这些相同的抗IR3抗体在EHV-1感染的细胞提取物中也未检测到IR3蛋白。这些发现表明IR3可能不会表达为蛋白质。未观察到IR3/GFP融合基因的表达,但通过荧光显微镜检测到了GFP/IR3融合基因的表达。在进一步尝试使用抗GFP抗体检测IR3/GFP融合蛋白时,蛋白质印迹分析表明在体内未检测到IR3/GFP融合蛋白。有趣的是,从GFP/IR3融合基因合成了一种截短形式的GFP/IR3蛋白。然而,通过融合基因的体外偶联转录和翻译合成了预测大小的GFP/IR3和IR3/GFP融合蛋白,这表明IR3蛋白在体内表达不佳。讨论了IR3转录本在EHV-1感染中的可能作用。