Wathen M W, Hay J
J Virol. 1984 Jul;51(1):237-41. doi: 10.1128/JVI.51.1.237-241.1984.
The nuc- lesion affecting alkaline exonuclease activity in the herpes simplex virus type 2 (HSV-2) mutant ts1348 had previously been mapped to the EcoRI-D restriction enzyme fragment of HSV-1. Eight clones with deletions representing most of HSV-1 EcoRI fragment D were selected with lambda gtWES hybrids. These clones were tested for their ability to rescue the alkaline exonuclease activity of HSV-2 nuc- ts1348 virus. The sequences colinear with the HSV-2 nuc- lesion were found to map between 0.169 and 0.174 map units on the HSV-1 Patton genome, representing an 0.8-kilobase-pair region that is 12.9 to 13.7 kilobase pairs from the left end of HSV-1 EcoRI fragment D.
影响单纯疱疹病毒2型(HSV - 2)突变体ts1348碱性核酸外切酶活性的nuc病变先前已被定位到HSV - 1的EcoRI - D限制性酶切片段上。用λgtWES杂种筛选出8个代表HSV - 1 EcoRI片段D大部分区域缺失的克隆。测试了这些克隆拯救HSV - 2 nuc - ts1348病毒碱性核酸外切酶活性的能力。发现与HSV - 2 nuc病变共线的序列位于HSV - 1帕顿基因组上0.169至0.174个图谱单位之间,代表一个0.8千碱基对的区域,该区域距离HSV - 1 EcoRI片段D的左端12.9至13.7千碱基对。