Knebel-Mörsdorf D, Kremer A, Jahnel F
Institute of Genetics, University of Cologne, Germany.
J Virol. 1993 Feb;67(2):753-8. doi: 10.1128/JVI.67.2.753-758.1993.
We have been investigating the first viral genes to be transcribed in Spodoptera frugiperda cells after the infection with Autographa california nuclear polyhedrosis virus in order to identify regulatory proteins required for the activation of early and/or late gene transcription. By screening a cDNA library from polyadenylated RNA transcribed at 1 h postinfection, we identified a gene which is designated ME53. This newly identified gene is located upstream of the late p74 gene and forms a divergent promoter unit with the immediate-early gene IE0. The determination of the nucleotide sequence of ME53 has revealed an open reading frame encoding a gene product of 53 kDa. Furthermore, the sequence data suggest a putative DNA binding motif, a zinc finger, whose functional significance has yet to be shown. Transcription of ME53 does not require previous viral protein synthesis, and during infection, the level of promoter activity seems to be independent of trans-acting viral factors, as suggested by transient expression studies.
我们一直在研究草地贪夜蛾细胞在感染苜蓿银纹夜蛾核型多角体病毒后最早转录的病毒基因,以鉴定激活早期和/或晚期基因转录所需的调控蛋白。通过筛选感染后1小时转录的聚腺苷酸化RNA的cDNA文库,我们鉴定出一个名为ME53的基因。这个新鉴定的基因位于晚期p74基因的上游,并与立即早期基因IE0形成一个反向启动子单元。ME53核苷酸序列的测定揭示了一个编码53 kDa基因产物的开放阅读框。此外,序列数据表明存在一个假定的DNA结合基序,即锌指结构,其功能意义尚待揭示。ME53的转录不需要先前的病毒蛋白合成,并且在感染过程中,如瞬时表达研究所表明的,启动子活性水平似乎独立于反式作用病毒因子。