Stewart Meredith E, Desport Moira, Setiyaningsih Surachmi, Hartaningsih Nining, Wilcox Graham E
School of Veterinary and Biomedical Science, Murdoch University, Murdoch, South Street, Perth, WA 6150, Australia.
Virus Res. 2008 Aug;135(2):336-9. doi: 10.1016/j.virusres.2008.03.017. Epub 2008 May 7.
Jembrana disease virus (JDV) is an unusual bovine lentivirus that causes an acute disease syndrome with a 20% case fatality rate after a short incubation period in Bos javanicus (Bali cattle) in Indonesia. Analysis of tat mRNA transcription patterns has identified up to six differently spliced transcripts indicating that, in common with other lentiviruses, JDV uses a complex splicing pattern. RT-PCR analysis of mRNA transcripts produced during the acute phase of infection with JDV(TAB/87) revealed at least 12 differently spliced transcripts involving 9 different splice sites. A single unspliced gag/pol transcript, singly spliced vif and tmx specific transcripts and alternatively spliced env, tat and rev transcripts were identified. A 67 nucleotide putative non-coding exon was identified that shared the same splice acceptor (SA) as vif and was incorporated into alternative transcripts of tat, rev and env.
杰姆巴纳病病毒(JDV)是一种不同寻常的牛慢病毒,在印度尼西亚的爪哇牛(巴厘牛)中,经过短暂潜伏期后会引发一种急性疾病综合征,病死率达20%。对tat mRNA转录模式的分析已鉴定出多达六种不同剪接的转录本,这表明与其他慢病毒一样,JDV采用复杂的剪接模式。对感染JDV(TAB/87)急性期产生的mRNA转录本进行的RT-PCR分析显示,至少有12种不同剪接的转录本,涉及9个不同的剪接位点。鉴定出了一个单一的未剪接gag/pol转录本、单独剪接的vif和tmx特异性转录本以及选择性剪接的env、tat和rev转录本。鉴定出一个67个核苷酸的推定非编码外显子,它与vif共享相同的剪接受体(SA),并被纳入tat、rev和env的可变转录本中。