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来自人类巨细胞病毒立即早期区域2的多个剪接和未剪接转录本以及立即早期区域1内共同起始位点的证据。

Multiple spliced and unspliced transcripts from human cytomegalovirus immediate-early region 2 and evidence for a common initiation site within immediate-early region 1.

作者信息

Stenberg R M, Witte P R, Stinski M F

出版信息

J Virol. 1985 Dec;56(3):665-75. doi: 10.1128/JVI.56.3.665-675.1985.

DOI:10.1128/JVI.56.3.665-675.1985
PMID:2999423
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC252635/
Abstract

Human cytomegalovirus immediate-early (IE) region 2 (0.732 to 0.740 map unit) begins 35 nucleotides downstream of IE region 1 (Stenberg et al., J. Virol. 49:190-199, 1984). A series of mRNAs that have different splicing patterns are transcribed from region 2. There is an unspliced 1,589-nucleotide exon present in minor amounts and two spliced exons (836 and 289 nucleotides) present in larger amounts. The IE region 2 exons were found to be spliced onto the first three exons of region 1. Therefore, under IE conditions the region 1 promoter-regulatory region can promote transcription of region 2. Promoter sequences (i.e., CAAT and TATA boxes) are found upstream of the 5' end of IE region 2 but presumably function poorly at IE times after infection. The transcriptional regulation of these IE genes and the possible functional roles of the proteins are discussed. We postulate that a series of unique but related proteins are made from the region 2 transcripts. Some of these proteins should contain the same 169 amino-terminal residues as the major IE 72-kilodalton protein encoded by IE region 1 (Stenberg et al., J. Virol. 49:190-199, 1984). Variations in the amino acid sequences of the region 2 proteins could occur at either the amino terminus, the carboxy terminus, or both termini.

摘要

人巨细胞病毒即刻早期(IE)区域2(图谱单位0.732至0.740)起始于IE区域1下游35个核苷酸处(斯滕伯格等人,《病毒学杂志》49:190 - 199,1984年)。从区域2转录出一系列具有不同剪接模式的mRNA。存在少量未剪接的1589个核苷酸的外显子以及大量剪接的外显子(836和289个核苷酸)。发现IE区域2的外显子被剪接到区域1的前三个外显子上。因此,在IE条件下,区域1启动子 - 调控区域可促进区域2的转录。在IE区域2的5'端上游发现了启动子序列(即CAAT盒和TATA盒),但推测在感染后的IE时期功能不佳。讨论了这些IE基因的转录调控以及蛋白质可能的功能作用。我们推测从区域2转录本产生一系列独特但相关的蛋白质。其中一些蛋白质应与IE区域1编码的主要IE 72千道尔顿蛋白质含有相同的169个氨基末端残基(斯滕伯格等人,《病毒学杂志》49:190 - 199,1984年)。区域2蛋白质氨基酸序列的变异可能发生在氨基末端、羧基末端或两端。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/a4736ac68bf3/jvirol00117-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/3ad0f409367e/jvirol00117-0022-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/890979eeb6fd/jvirol00117-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/7e09217909b5/jvirol00117-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/a4736ac68bf3/jvirol00117-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/3ad0f409367e/jvirol00117-0022-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/890979eeb6fd/jvirol00117-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/7e09217909b5/jvirol00117-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b44/252635/a4736ac68bf3/jvirol00117-0028-a.jpg

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