Thierer J, Riehle H, Grebenstein O, Binz T, Herzog S, Thiedemann N, Stitz L, Rott R, Lottspeich F, Niemann H
Institut für Mikrobiologie, BFAV, Tübingen, Germany.
J Gen Virol. 1992 Feb;73 ( Pt 2):413-6. doi: 10.1099/0022-1317-73-2-413.
Based on partial amino acid sequences obtained from tryptic peptides of the purified 24K antigen of Borna disease virus (BDV), we identified and sequenced four independent cDNA clones established from BDV-infected MDCK cells. Each of the clones encodes a polypeptide of 201 residues (Mr 22461) that differs considerably from an amino acid sequence published recently. In vitro transcription/translation of both the wild-type and a 5' truncated clone lacking the first ATG codon yielded a peptide that comigrates on electrophoresis with a polypeptide immunoprecipitated from BDV-infected cells. The deduced amino acid sequence contains a putative signal for nuclear targeting.
基于从纯化的博尔纳病病毒(BDV)24K抗原的胰蛋白酶肽段获得的部分氨基酸序列,我们鉴定并测序了从BDV感染的MDCK细胞建立的四个独立的cDNA克隆。每个克隆编码一个201个残基(Mr 22461)的多肽,该多肽与最近发表的氨基酸序列有很大差异。野生型和缺少第一个ATG密码子的5'截短克隆的体外转录/翻译产生了一种在电泳中与从BDV感染细胞中免疫沉淀的多肽共迁移的肽。推导的氨基酸序列包含一个假定的核靶向信号。