Perng G C, Ghiasi H, Slanina S M, Nesburn A B, Wechsler S L
Ophthalmology Research Laboratories, Cedars-Sinai Medical Center Research Institute, Los Angeles, California 90048, USA.
J Virol. 1996 Feb;70(2):976-84. doi: 10.1128/JVI.70.2.976-984.1996.
The herpes simplex virus type 1 (HSV-1) latency-associated transcript (LAT) gene is essential for efficient spontaneous reactivation of HSV-1 from latency. We report here that although the LAT gene is 8.3 kb in length, the first 1.5 kb of the LAT gene alone is sufficient for wild-type levels of spontaneous reactivation. We began with a LAT deletion mutant of HSV-1 strain McKrae in which the LAT promoter and the first 1.6 kb of the 5' end of the LAT gene had been deleted from both copies of LAT (one in each viral long repeat). As we previously reported, this mutant (dLAT2903) was significantly impaired for spontaneous reactivation (G. C. Perng, E. C. Dunkel, P. A. Geary, S. M. Slanina, H. Ghiasi, R. Kaiwar, A. B. Nesburn, and S. L. Wechsler, J. Virol. 68:8045-8055, 1994). We then inserted the LAT promoter and the first 1.5 kb of the LAT gene into a location in the unique long region of dLAT2903 far removed from the normal location of LAT in the long repeats. This resulted in a virus (LAT15a) whose capacity for transcribing LAT RNA was limited to the first 1.5 kb of the 8.3-kb LAT primary transcript. Rabbits were ocularly infected with this mutant, and spontaneous reactivation was measured in comparison to those of the original LAT-negative mutant and its marker-rescued (wild-type) virus, dLAT2903R. LAT15a had an in vivo spontaneous reactivation rate of 12%, compared with a rate of 11% for the marker-rescued virus and 0% for the LAT-negative virus. Southern analysis confirmed that the spontaneously reactivated LAT15a virus retained the original deletions in both copies of LAT and the 1.5-kb LAT insertion in the unique long region. Thus, insertion of the first 1.5 kb of LAT (and its promoter) at a site distant from the normal LAT location appeared to completely restore in vivo spontaneous reactivation to wild-type levels, despite the remaining inability of the original LAT genes to transcribe any LAT RNA. The function of LAT involved in efficient spontaneous reactivation therefore appeared to map completely within the first 1.5 kb of the LAT gene.
单纯疱疹病毒1型(HSV-1)潜伏相关转录物(LAT)基因对于HSV-1从潜伏状态高效自发再激活至关重要。我们在此报告,尽管LAT基因长度为8.3 kb,但仅LAT基因的前1.5 kb就足以实现野生型水平的自发再激活。我们从HSV-1 McKrae株的一个LAT缺失突变体开始,在该突变体中,LAT启动子和LAT基因5'端的前1.6 kb已从LAT的两个拷贝(每个病毒长重复序列中的一个)中删除。正如我们之前报道的,这个突变体(dLAT2903)的自发再激活能力显著受损(G.C. Perng、E.C. Dunkel、P.A. Geary、S.M. Slanina、H. Ghiasi、R. Kaiwar、A.B. Nesburn和S.L. Wechsler,《病毒学杂志》68:8045 - 8055,1994年)。然后我们将LAT启动子和LAT基因的前1.5 kb插入到dLAT2903独特长区域中一个远离LAT在长重复序列中正常位置的位点。这产生了一种病毒(LAT15a),其转录LAT RNA的能力仅限于8.3 kb LAT初级转录物的前1.5 kb。用这种突变体对兔子进行眼部感染,并与原始的LAT阴性突变体及其标记拯救(野生型)病毒dLAT2903R相比,测量自发再激活情况。LAT15a的体内自发再激活率为12%,而标记拯救病毒的再激活率为11%,LAT阴性病毒的再激活率为0%。Southern分析证实,自发再激活的LAT15a病毒在LAT的两个拷贝中都保留了原始缺失,并且在独特长区域中有1.5 kb的LAT插入。因此,将LAT的前1.5 kb(及其启动子)插入到远离LAT正常位置的位点似乎能将体内自发再激活完全恢复到野生型水平,尽管原始LAT基因仍无法转录任何LAT RNA。因此,参与高效自发再激活的LAT功能似乎完全定位在LAT基因的前1.5 kb内。