Wagner E K, Devi-Rao G, Feldman L T, Dobson A T, Zhang Y F, Flanagan W M, Stevens J G
Department of Molecular Biology and Biochemistry, University of California, Irvine 92717.
J Virol. 1988 Apr;62(4):1194-202. doi: 10.1128/JVI.62.4.1194-1202.1988.
RNA transfer (Northern) blot analysis was used to perform the physical characterization of the transcript expressed in murine sensory nerve ganglia latently infected with herpes simplex virus type 1. Most of this latency-associated transcript (LAT) was isolated in the poly(A)- fraction from ganglia. A smaller RNA species was also detected at less than 10% the abundance of the major one. LAT was not detected with probes from DNA outside the limits of the larger species. In situ hybridization data correlated well with Northern blot analysis; however, low levels of hybridization were seen with probes immediately outside the region of viral DNA giving positive Northern blot signals. S1 nuclease and primer extension mapping were used to locate the 5' end of the LAT 510 bases to the left of a KpnI site at 0.783 map units. The 3' end of the major latency-associated species was mapped to just within a 310-base-pair SmaI fragment located 660 to 970 base pairs to the right of the SalI site at 0.790 map units. These data were correlated with an analysis of the sequence of the DNA encoding this transcript and its possible function in the latent phase of infection.
RNA转移(Northern)印迹分析用于对在潜伏感染1型单纯疱疹病毒的小鼠感觉神经节中表达的转录本进行物理特性鉴定。这种潜伏期相关转录本(LAT)的大部分是从神经节的聚腺苷酸(poly(A))组分中分离出来的。还检测到一种较小的RNA种类,其丰度不到主要种类的10%。用超出较大种类范围的DNA探针未检测到LAT。原位杂交数据与Northern印迹分析结果良好相关;然而,如果使用紧邻产生阳性Northern印迹信号的病毒DNA区域外部的探针,则会看到低水平的杂交信号。使用S1核酸酶和引物延伸图谱法将LAT的5'端定位在0.783图谱单位处KpnI位点左侧510个碱基处。主要潜伏期相关种类的3'端定位在位于0.790图谱单位处SalI位点右侧660至970个碱基对的一个310碱基对SmaI片段内。这些数据与对编码该转录本的DNA序列及其在潜伏感染期可能功能的分析相关联。