Tollefson A E, Krajcsi P, Pursley M H, Gooding L R, Wold W S
Institute for Molecular Virology, St. Louis University School of Medicine, Missouri 63110.
Virology. 1990 Mar;175(1):19-29. doi: 10.1016/0042-6822(90)90182-q.
There is an ORF in the early region E3 transcription unit of human adenovirus 5 (Ad5) which could encode a protein of 14,500 MW (14.5K). This ORF is conserved in Ad5 and Ad2, both group C adenoviruses, and also in Ad3 and Ad7, both group B adenoviruses. To address whether the 14.5K protein is synthesized, we prepared antisera against synthetic peptides corresponding to residues 19-34 or 118-132 in the Ad5 version of 14.5K, and also against a TrpE-14.5K fusion protein expressed in Escherichia coli. These antisera immunoprecipitated the [35S]Met-labeled 14.5K protein from KB cells infected with rec700 (an Ad5-Ad2-Ad5 recombinant), Ad2, and a variety of E3 mutants. Mutants in the 14.5K ORF did not produce the 14.5K protein. The 14.5K is coded in large part, although probably not exclusively, by E3 mRNA f, as indicated by immunoprecipitation of 14.5K from cells infected with mutants that overproduce or underproduce mRNA f. The 14.5K migrated as five to six bands on SDS-PAGE after immunoprecipitation or Western blot, suggesting that it undergoes post-translational modification. Two bands of 14.5K were obtained by cell-free translation of 14.5K from mRNA purified by hybridization from infected cells.
人腺病毒5型(Ad5)早期区域E3转录单元中存在一个开放阅读框(ORF),它可以编码一种分子量为14,500道尔顿(14.5K)的蛋白质。这个ORF在Ad5和Ad2(均为C组腺病毒)以及Ad3和Ad7(均为B组腺病毒)中保守。为了研究14.5K蛋白是否被合成,我们制备了针对与Ad5版本14.5K中第19 - 34位或118 - 132位残基对应的合成肽的抗血清,以及针对在大肠杆菌中表达的TrpE - 14.5K融合蛋白的抗血清。这些抗血清从感染rec700(一种Ad5 - Ad2 - Ad5重组体)、Ad2和多种E3突变体的KB细胞中免疫沉淀出[35S]甲硫氨酸标记的14.5K蛋白。14.5K ORF中的突变体不产生14.5K蛋白。如从过量产生或产生不足mRNA f的突变体感染的细胞中免疫沉淀14.5K所示,14.5K大部分(尽管可能不是全部)由E3 mRNA f编码。免疫沉淀或蛋白质印迹后,14.5K在SDS - PAGE上迁移为五到六条带,表明它经历了翻译后修饰。通过从感染细胞杂交纯化的mRNA对14.5K进行无细胞翻译,获得了两条14.5K带。