Ruvolo V R, Berneman Z, Secchiero P, Nicholas J
Johns Hopkins Oncology Center, Baltimore, Maryland 21231, USA.
J Gen Virol. 1996 Aug;77 ( Pt 8):1901-12. doi: 10.1099/0022-1317-77-8-1901.
Human herpesvirus 7 (HHV-7) is a recently isolated herpesvirus that has been shown to be related to human cytomegalovirus and human herpesvirus 6 and to be a member of the betaherpesvirus subgroup. Here we report the cloning, restriction endonuclease mapping and partial sequence analysis of HHV-7 strain JI DNA. Virus particles were obtained from the supernatant of infected SupT1 cells, the DNA isolated by proteinase K treatment-phenol extraction, and full-length viral DNA was purified and isolated on a pulsed-field gel. Aliquots of this highly purified material were treated in the following ways: (i) sonicated and end-repaired to create short randomly sheared fragments for cloning into M13mp 18-Smal vector DNA; (ii) cut with EcoRI for cloning into EcoRI-cut lambda ZAPII or lambda DASHII vectors; (iii) cut with BamHI for cloning into BamHI-cut lambda ZAP-Express or lambda DASHII vectors. Partial nucleotide sequencing of the M13 clones followed by detection of open reading frames and their translation allowed the identification of homologues through FASTA searches of the database. Relevant M13 clones were used as probes to isolate corresponding lambda phage clones, which could tentatively be mapped to the genome on the basis of presumed genetic collinearity between HHV-7 and HHV-6. Genomic "walking' between EcoRI and BamHI lambda genomic libraries enabled overlapping neighbouring clones to be identified and mapped. Each of these clones was analysed to map BamHI, EcoRI, Sa/l, Smal and Xhol restriction endonuclease sites to provide complete endonuclease maps for the entire genome.
人类疱疹病毒7型(HHV - 7)是一种最近分离出的疱疹病毒,已被证明与人类巨细胞病毒和人类疱疹病毒6型有关,是β疱疹病毒亚组的成员。在此,我们报告HHV - 7 JI株DNA的克隆、限制性内切酶图谱分析及部分序列分析。病毒颗粒从感染的SupT1细胞上清液中获得,通过蛋白酶K处理 - 酚抽提法分离DNA,然后在脉冲场凝胶上纯化并分离全长病毒DNA。对这种高度纯化的材料进行如下处理:(i)超声处理并进行末端修复,以产生随机剪切的短片段,用于克隆到M13mp 18 - Smal载体DNA中;(ii)用EcoRI切割,用于克隆到经EcoRI切割的λZAPII或λDASHII载体中;(iii)用BamHI切割,用于克隆到经BamHI切割的λZAP - Express或λDASHII载体中。对M13克隆进行部分核苷酸测序,随后检测开放阅读框及其翻译产物,通过数据库的FASTA搜索来鉴定同源物。相关的M13克隆用作探针,以分离相应的λ噬菌体克隆,根据HHV - 7和HHV - 6之间假定的基因共线性,这些克隆可初步定位到基因组上。在EcoRI和BamHI λ基因组文库之间进行基因组“步移”,可鉴定并定位重叠的相邻克隆。对每个克隆进行分析,以定位BamHI、EcoRI、SalI、Smal和Xhol限制性内切酶位点,从而为整个基因组提供完整的内切酶图谱。