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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Gene arrangement and RNA transcription of the BamHI fragments K and M2 within the non-oncogenic Marek's disease virus serotype 2 unique long genome region.
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Gene arrangement and RNA transcription of the BamHI fragments K and M2 within the non-oncogenic Marek's disease virus serotype 2 unique long genome region.

机译:基因排列和RNA的转录在non-oncogenic BamHI碎片K和M2马立克氏病病毒血清型2独特的长基因组区域。

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摘要

We determined the nucleotide sequence of a 6593 bp fragment of the Marek's disease virus serotype 2 (MDV2) unique long region located in the right part of genomic BamHI-M2 and the adjacent part of BamHI-K fragments. Within this region five complete open reading frames (ORFs) were identified whose deduced amino acid sequences exhibited homology to the UL53 (glycoprotein K), UL54 (immediate early regulatory protein ICP27), and UL55 gene products of herpes simplex virus type 1 (HSV-1). Homologue to the HSV-1 UL56 was not detected. However, we identified a gene between the MDV2 UL54 and UL55 genes with homology to the first ORF (ORF-1) of equine herpesvirus type 1 and corresponding gene identified in pseudorabies virus. Two adjacent ORFs contained in the BamHI-K fragment, ORF 873s and ORF 873, were found by computer analysis to have the properties of an intron encoding a glycoprotein: ORF 873s encodes a 84 amino acid polypeptide with a stretch of a hydrophobic signal sequence in the C-terminus, and ORF 873 encodes a 873 amino acid polypeptide with a transmembrane domain and putative three N-linked glycosylation sites. All the identified genes were confirmed to be transcribed with 3'-coterminal transcripts and/or a unique transcript in the virus-infected cells. Especially, 3.5 kb mRNA of ORF 873s and ORF 873 are transcribed from a potential promoter region of ORF 873s, and splice donor and acceptor sites are used to splice the mRNA after cleavage of a 113 bp-nucleotide sequence.
机译:我们确定了6593个基点的核苷酸序列马立克氏病病毒血清型2的片段(MDV2)独特的长地区位于右边基因组的一部分BamHI-M2和相邻的部分BamHI-K碎片。完整的开放阅读框(orf)推导的氨基酸序列的识别表现出相同的UL53(糖蛋白K),UL54(即早期监管蛋白质ICP27),和UL55单纯疱疹病毒的基因产物1型(1型单纯疱疹病毒)。没有检测到。之间的MDV2 UL54和UL55基因同源性第一个ORF (ORF-1)的马疱疹病毒1型和相应的基因识别假狂犬病病毒。ORF BamHI-K片段中包含,873年代开放873年开放,是由电脑分析发现的有一个内含子编码的属性吗糖蛋白:873年代ORF编码84个氨基酸多肽的疏水性在糖基信号序列,ORF 873编码873个氨基酸的多肽三N-linked跨膜域和假定的糖基化的网站。被证实是转录3 '共终端的成绩单和/或一个独特成绩单在感染病毒的细胞。特别是3.5 kb mRNA的ORF 873年代和873年羊痘疮从一个潜在的转录启动子区域ORF 873年代,拼接供体和受体网站用于拼接的mRNA在乳沟吗113年bp-nucleotide序列。

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