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

Citation
Y. Tsushima et al., 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, VIRUS RES, 60(1), 1999, pp. 101-110
Citations number
26
Categorie Soggetti
Microbiology
Journal title
VIRUS RESEARCH
ISSN journal
01681702 → ACNP
Volume
60
Issue
1
Year of publication
1999
Pages
101 - 110
Database
ISI
SICI code
0168-1702(199903)60:1<101:GAARTO>2.0.ZU;2-L
Abstract
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 par t of genomic BamHI-M2 and the adjacent part of BamHI-K fragments. Within th is region five complete open reading frames (ORFs) were identified whose de duced 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 d etected. 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 co rresponding gene identified in pseudorabies virus. Two adjacent ORFs contai ned in the BamHI-K fragment, ORF 873s and ORF 873, were found by computer a nalysis to have the properties of an intron encoding a glycoprotein: ORF 87 3s encodes a 84 amino acid polypeptide with a stretch of a hydrophobic sign al sequence in the C-terminus, and ORF 873 encodes a 873 amino acid polypep tide with a transmembrane domain and putative three N-linked glycosylation sites. All the identified genes were confirmed to be transcribed with 3'-co terminal 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 po tential promoter region of ORF 873s, and splice donor and acceptor sites ar e used to splice the mRNA after cleavage of a 113 bp-nucleotide sequence. ( C) 1999 Elsevier Science B.V. All rights reserved.