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Regulated expression of early and late RNAs and proteins from the human cytomegalovirus immediate-early gene region.

机译:调节人类巨细胞病毒即早基因区域中早期和晚期RNA和蛋白质的表达。

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摘要

Expression of RNA and protein from the human cytomegalovirus immediate-early (IE) gene region (map units 0.732 to 0.751) was analyzed at early and late times after infection. The level of RNA present at late times (48 to 72 h after infection) was significantly higher than that present at IE times (5 h after infection). The profile of IE RNA in the cytoplasm of infected cells was different from that previously reported on polysomes (R. M. Stenberg, P. R. Witte, and M. F. Stinski, J. Virol. 56:665-675, 1985). The data indicate that the 1.95-kilobase (kb) major IE region 1 mRNA, which codes for the 72-kilodalton (kDa) protein, and the 1.7-kb IE region 2 (IE2) spliced mRNA, which codes for the IE2 55-kDa protein, may be preferentially associated with polysomes. However, the IE2 2.2-kb unspliced mRNA, which codes for an 86-kDa protein, may be preferentially excluded. This RNA was abundant in the cytoplasm under IE conditions but was not present on polysomes in significant quantities. This indicates that IE gene products may be involved in translational control of cytomegalovirus RNA. At late times, new transcription takes place within region 2. A 1.5-kb RNA is transcribed from a late promoter in region 2 that apparently does not function in cells infected with DNA-negative mutant ts66. These results demonstrate that the IE gene region is transcribed throughout infection and that multiple levels of regulation exist.
机译:在感染后的早期和晚期,分析了人类巨细胞病毒即早(IE)基因区域(图单元0.732至0.751)中RNA和蛋白质的表达。晚期(感染后48至72小时)存在的RNA水平显着高于IE时期(感染后5小时)存在的RNA水平。 IE RNA在被感染细胞的细胞质中的分布与先前在多核糖体上报道的不同(R. M. Stenberg,P。R. Witte和M. F. Stinski,J。Virol。56:665-675,1985)。数据表明,编码72-千达尔顿(kDa)蛋白的1.95碱基对(kb)主要IE区1 mRNA,和编码IE2 55-的1.7-kb IE区2(IE2)剪接的mRNA。 kDa蛋白可能优先与多核糖体相关。但是,可以优先排除编码86-kDa蛋白质的IE2 2.2 kb未剪接的mRNA。在IE条件下,该RNA在细胞质中丰富,但在多核糖体上却不大量存在。这表明IE基因产物可能参与巨细胞病毒RNA的翻译控制。在晚期,新的转录发生在区域2中。从区域2中的晚期启动子转录了一个1.5 kb的RNA,该启动子显然在被DNA阴性突变体ts66感染的细胞中不起作用。这些结果表明,IE基因区域在整个感染过程中都被转录,并且存在多种水平的调控。

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