Stow N D, McMonagle E C
Virology. 1983 Oct 30;130(2):427-38. doi: 10.1016/0042-6822(83)90097-1.
In previous experiments, an origin of viral DNA replication was localized within a 995-bp DNA fragment that mapped entirely within the TRS/IRS repeated region of the herpes simplex virus type 1 genome (N. D. Stow, EMBO J. 1, 863-867, 1982). In this paper, this origin is now shown to reside within a 535-bp segment subcloned from the above fragment. Deletions extending various distances into each end of the 535-bp segment were generated using nuclease BAL 31, and the resulting plasmids screened for their ability to replicate in cells superinfected with wild-type HSV-1 helper virus. This analysis indicated that the cis-acting sequences essential for DNA replication were present within a 90-bp region, and a 100-bp viral DNA fragment containing all the signals necessary for origin function was identified. The origin lies within an untranscribed region located between the 5'-ends of two divergently transcribed immediate-early mRNAs. A prominant feature of the origin region is an almost perfect palindromic sequence 45 bp long containing 18 consecutive A or T residues at its center.
在先前的实验中,病毒DNA复制起点定位于一个995碱基对的DNA片段内,该片段完全位于单纯疱疹病毒1型基因组的TRS/IRS重复区域内(N.D.斯托,《欧洲分子生物学组织杂志》1,863 - 867,1982年)。在本文中,现已表明该起点位于从上述片段亚克隆的一个535碱基对的区段内。使用核酸酶BAL 31产生了向535碱基对区段两端延伸不同距离的缺失,然后筛选所得质粒在被野生型HSV - 1辅助病毒超感染的细胞中进行复制的能力。该分析表明,DNA复制所必需的顺式作用序列存在于一个90碱基对的区域内,并且鉴定出了一个包含起点功能所需所有信号的100碱基对病毒DNA片段。该起点位于两个反向转录的立即早期mRNA的5'端之间的一个未转录区域内。起点区域的一个显著特征是一个几乎完美的45碱基对回文序列,其中心含有18个连续的A或T残基。