Broer R, Heldens J G, van Strien E A, Zuidema D, Vlak J M
Department of Virology, Wageningen Agricultural University, The Netherlands.
J Gen Virol. 1998 Jun;79 ( Pt 6):1563-72. doi: 10.1099/0022-1317-79-6-1563.
The region upstream of the Spodoptera exigua multicapsid nucleopolyhedrovirus (SeMNPV) ubiquitin gene contains four near-identical 68-bp-long palindromic repeats. This region, named Sehr6 and located at map unit (m.u.) 88 of the SeMNPV genome on pSeEcoRI-2.2, showed structural homology to previously identified homologous regions (hrs) in a number of other baculoviruses. Hrs function as enhancers of transcription and as putative origins (oris) of baculovirus DNA replication. Five additional hrs (Sehr1-Sehr5) were identified on the SeMNPV genome by Southern blot hybridization with an 18-bp-long oligonucleotide complementary to a sequence conserved within the arms of the four palindromic repeats of Sehr6. Sehr1-Sehr6 were dispersed on the SeMNPV genome at m.u. 8.0, 30.0, 38.5, 51.0, 77.0 and 88.0, respectively. Sequence analysis of these hrs confirmed the presence of palindromic repeats, highly similar to those found in pSeEcoRI-2.2. The number of palindromes varied from one (Sehr4) to nine (Sehr1) per hr. The Sehrs are all present in non-coding regions of the SeMNPV genome and also contain multiple putative transcription recognition sequences. Plasmids containing either of the Sehrs replicated in an SeMNPV-dependent DNA replication assay. The Sehrs were unable to replicate in an AcMNPV-dependent DNA replication assay. This was in contrast to the previously observed SeMNPV non-hr type ori, which replicated in the presence of both AcMNPV and SeMNPV. These data suggest that the replication of SeMNPV and the role of hrs in this process is highly specific.
甜菜夜蛾多粒包埋核型多角体病毒(SeMNPV)泛素基因上游区域包含四个长度为68bp、近乎相同的回文重复序列。该区域命名为Sehr6,位于pSeEcoRI - 2.2上SeMNPV基因组的图谱单位(m.u.)88处,与其他多种杆状病毒中先前鉴定出的同源区域(hrs)具有结构同源性。Hrs作为转录增强子以及杆状病毒DNA复制的假定起始位点(oris)发挥作用。通过与一条18bp长的寡核苷酸进行Southern杂交,该寡核苷酸与Sehr6四个回文重复序列臂内保守序列互补,在SeMNPV基因组上鉴定出另外五个hrs(Sehr1 - Sehr5)。Sehr1 - Sehr6分别分散在SeMNPV基因组的m.u. 8.0、30.0、38.5、51.0、77.0和88.0处。对这些hrs的序列分析证实存在回文重复序列,与在pSeEcoRI - 2.2中发现的序列高度相似。每个hrs的回文数从1个(Sehr4)到9个(Sehr1)不等。Sehrs均存在于SeMNPV基因组的非编码区域,并且还包含多个假定的转录识别序列。在SeMNPV依赖性DNA复制试验中,含有任一Sehrs的质粒均可复制。在AcMNPV依赖性DNA复制试验中,Sehrs无法复制。这与先前观察到的SeMNPV非hr型ori相反,后者在AcMNPV和SeMNPV同时存在时均可复制。这些数据表明SeMNPV的复制以及hrs在此过程中的作用具有高度特异性。