Kang W, Suzuki M, Zemskov E, Okano K, Maeda S
Laboratory of Molecular Entomology, RIKEN (The Institute of Physical and Chemical Research), Wako, Japan.
J Virol. 1999 Dec;73(12):10339-45. doi: 10.1128/JVI.73.12.10339-10345.1999.
The baculovirus Bombyx mori nucleopolyhedrovirus (BmNPV) contains five related open reading frames (ORFs). Recent sequence analyses of several other baculovirus genomes reveal that these ORFs belong to a unique multigene family called the baculovirus repeated ORFs (bro) family. Here we have characterized these five genes from BmNPV at the transcriptional and translational levels. Reverse transcription-PCR and primer extension analyses indicated that transcription of all bro genes occurs by 2 to 4 h postinfection (p.i.) and reaches maximal levels between at 8 and 12 h p.i. Transcription of all genes is initiated between 50 and 70 nucleotides upstream of the start codon, at a characteristic C(T)AGT motif. Expression of a cat reporter gene under the control of each bro promoter provides evidence that a viral factor(s) is required for the transcription of all bro genes. Immunoblot analysis indicated that a population of BRO proteins is produced vigorously between at 8 and 14 h p.i. Immunohistochemical analysis by confocal microscopy showed that BRO proteins are localized in both the nucleus and the cytoplasm at 8 h p.i. Four BmNPV mutants, in which the bro-a, bro-b, bro-c, and bro-e genes were individually inactivated, were successfully isolated. However, exhaustive efforts failed to isolate a bro-d-deficient mutant. Similarly, it was not possible to isolate a double-deletion bro-a bro-c mutant. The bro-d gene may play an irreplaceable functional role(s) during viral infection, while bro-a and bro-c may functionally complement each other.
杆状病毒家蚕核型多角体病毒(BmNPV)包含五个相关的开放阅读框(ORF)。最近对其他几种杆状病毒基因组的序列分析表明,这些ORF属于一个独特的多基因家族,称为杆状病毒重复ORF(bro)家族。在此,我们在转录和翻译水平上对来自BmNPV的这五个基因进行了表征。逆转录PCR和引物延伸分析表明,所有bro基因的转录在感染后2至4小时发生,并在感染后8至12小时达到最高水平。所有基因的转录均在起始密码子上游50至70个核苷酸之间,在一个特征性的C(T)AGT基序处起始。在每个bro启动子控制下的cat报告基因的表达提供了证据,表明所有bro基因的转录需要一种病毒因子。免疫印迹分析表明,在感染后8至14小时大量产生BRO蛋白群体。通过共聚焦显微镜进行的免疫组织化学分析表明,在感染后8小时BRO蛋白定位于细胞核和细胞质中。成功分离出四个BmNPV突变体,其中bro-a、bro-b、bro-c和bro-e基因分别被灭活。然而,经过详尽的努力未能分离出bro-d缺陷型突变体。同样,也不可能分离出双缺失的bro-a bro-c突变体。bro-d基因可能在病毒感染期间发挥不可替代的功能作用,而bro-a和bro-c可能在功能上相互补充。