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伪狂犬病病毒潜伏基因和早期蛋白0基因的克隆

Cloning of the latency gene and the early protein 0 gene of pseudorabies virus.

作者信息

Cheung A K

机构信息

Virology Swine Research Unit, U.S. Department of Agriculture, Ames, Iowa 50010.

出版信息

J Virol. 1991 Oct;65(10):5260-71. doi: 10.1128/JVI.65.10.5260-5271.1991.

Abstract

A collection of overlapping cDNA clones encoding the latency transcript of pseudorabies virus and the DNA nucleotide sequence of the latency gene has been obtained. The transcript is spliced with 4.6 kb of intervening sequences. This mRNA, designated the large latency transcript, is 8.5 kb. It is polyadenylated and contains a large open reading frame capable of coding for a 200-kDa polypeptide. The direction of transcription is antiparallel to that of the immediate-early gene IE180 and a newly identified early gene, EP0. The latency transcript overlaps the entire IE180 gene and most of the EP0 gene. The EP0 mRNA is 1.75 kb and polyadenylated. The deduced amino acid sequence revealed the presence of cysteine-rich zinc finger domain similar to that of the immediate-early gene ICP0 of herpes simplex virus type 1 and the gene 61 polypeptide of varicella-zoster virus. On the basis of the biological functions, conserved protein domains, and unique spatial arrangements of the homologous polypeptides (IE180 versus ICP4 and EP0 versus ICP0) between pseudorabies virus and herpes simplex virus type 1, it is predicted that a homologous protein domain is also encoded by the 8.5-kb large latency transcripts of these two viruses.

摘要

已获得一组重叠的cDNA克隆,其编码伪狂犬病病毒的潜伏转录本以及潜伏基因的DNA核苷酸序列。该转录本与4.6 kb的间隔序列进行了剪接。这种mRNA被命名为大潜伏转录本,长度为8.5 kb。它进行了多聚腺苷酸化,并且包含一个能够编码200 kDa多肽的大开放阅读框。转录方向与立即早期基因IE180和新鉴定的早期基因EP0的转录方向相反。潜伏转录本与整个IE180基因和大部分EP0基因重叠。EP0 mRNA为1.75 kb且进行了多聚腺苷酸化。推导的氨基酸序列显示存在富含半胱氨酸的锌指结构域,类似于单纯疱疹病毒1型的立即早期基因ICP0和水痘-带状疱疹病毒的基因61多肽。基于伪狂犬病病毒和单纯疱疹病毒1型之间同源多肽(IE180与ICP4以及EP0与ICP0)的生物学功能、保守蛋白结构域和独特空间排列,预测这两种病毒的8.5 kb大潜伏转录本也编码一个同源蛋白结构域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d55/249005/8baf01eaf8f4/jvirol00053-0146-a.jpg

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