Kovacs G R, Guarino L A, Summers M D
Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843.
J Virol. 1991 Oct;65(10):5281-8. doi: 10.1128/JVI.65.10.5281-5288.1991.
The baculovirus Autographa californica multicapsid nuclear polyhedrosis virus expresses two immediate-early genes from the HindIII-G region (map units 90.4 to 96.8) of the genome. During the early phase of infection, nonspliced 1.9-kb and spliced 2.1-kb transcripts are expressed which encode the IE1 and IE0 (spliced IE1) gene products, respectively. These two gene products differ only in that IE0 contains an additional 54 amino acids at the amino terminus. RNA analysis of these two genes during infection revealed that they were differentially expressed. IE1 was expressed early and late, whereas IE0 was expressed only early in infection. The regulation of these two immediate-early genes was analyzed by transient expression assays. The IE1 gene product stimulated expression of IE1 promoter-directed expression but down-regulated expression from the IE0 promoter. The IE0 gene product also transactivated the IE1 promoter but did not affect expression from its own promoter. Unlike IE1, which transactivates the delayed early 39K gene in the presence and absence of the homologous region (hr) enhancers, IE0 transactivated the 39K promoter only in the presence of cis-linked hr5 enhancer. The results of this study in conjunction with previous results suggest that the IE1 gene encodes a multifunctional gene product that may be involved in (i) repression of immediate-early gene expression, (ii) continued expression of its own gene product during infection, and (iii) transactivation of the delayed early and late classes of genes.
苜蓿银纹夜蛾多核衣壳核型多角体病毒(Autographa californica multicapsid nuclear polyhedrosis virus)表达来自基因组HindIII - G区域(图谱单位90.4至96.8)的两个立即早期基因。在感染早期,表达了未剪接的1.9 kb和剪接的2.1 kb转录本,它们分别编码IE1和IE0(剪接的IE1)基因产物。这两种基因产物的区别仅在于IE0在氨基末端含有额外的54个氨基酸。感染期间对这两个基因的RNA分析表明它们是差异表达的。IE1在感染的早期和晚期都有表达,而IE0仅在感染早期表达。通过瞬时表达分析对这两个立即早期基因的调控进行了研究。IE1基因产物刺激了IE1启动子指导的表达,但下调了IE0启动子的表达。IE0基因产物也反式激活了IE1启动子,但不影响其自身启动子的表达。与IE1不同,IE1在存在和不存在同源区域(hr)增强子的情况下都能反式激活延迟早期39K基因,而IE0仅在存在顺式连接的hr5增强子时才能反式激活39K启动子。本研究结果与先前结果表明,IE1基因编码一种多功能基因产物,可能参与:(i)立即早期基因表达的抑制;(ii)感染期间其自身基因产物的持续表达;(iii)延迟早期和晚期基因类别的反式激活。