Weber J M, Anderson C W
Départment de Microbiologie, Faculté de Médecine Université de Sherbrooke, Québec, Canada.
J Virol. 1988 May;62(5):1741-5. doi: 10.1128/JVI.62.5.1741-1745.1988.
Nucleoprotein complexes extracted from infected cells (J. Weber and L. Philipson, Virology 136:321-327, 1984) or ts1 virions grown at 39 degrees C (J. M. Weber, G. Khitto, and A. R. Bhatti, Can. J. Microbiol. 29:235-241, 1983) contain, in addition to known virion proteins, a polypeptide with a molecular weight of 11,000 (11K polypeptide). We identified the gene for this polypeptide by sequence analysis of the radioactively labeled 11K polypeptide isolated from ts1 virions and comparison of this sequence with the nucleotide sequence of the adenovirus type 2 genome. The 11K polypeptide was encoded by an open reading frame of 80 residues located between nucleotides 17,676 and 17,915 in late transcription region 2 of adenovirus type 2; the initiating methionine residue was removed leaving a 79-residue product. The late transcription region 2 that encoded the 79-residue polypeptide (11K) was arginine rich (21%) and had a predicted molecular weight of 8,715. It was cleaved by the viral endoprotease to give two products which comigrated on sodium dodecyl sulfate-polyacrylamide gels as virion polypeptide X. Our data suggest that additional cleavage of the carboxy-terminal 48-residue fragment generates a 19-amino-acid fragment with the amino acid composition of mu (K. Hosokawa and M. T. Sung, J. Virol. 17:924-934, 1976).
从受感染细胞中提取的核蛋白复合物(J. 韦伯和L. 菲利普森,《病毒学》136:321 - 327,1984年)或在39摄氏度下培养的ts1病毒粒子(J. M. 韦伯、G. 基托和A. R. 巴蒂,《加拿大微生物学杂志》29:235 - 241,1983年),除了已知的病毒粒子蛋白外,还含有一种分子量为11,000的多肽(11K多肽)。我们通过对从ts1病毒粒子中分离出的放射性标记的11K多肽进行序列分析,并将该序列与腺病毒2型基因组的核苷酸序列进行比较,确定了该多肽的基因。11K多肽由位于腺病毒2型晚期转录区2中核苷酸17,676和17,915之间的一个80个残基的开放阅读框编码;起始甲硫氨酸残基被去除,留下一个79个残基的产物。编码79个残基多肽(11K)的晚期转录区2富含精氨酸(21%),预测分子量为8,715。它被病毒内蛋白酶切割成两种产物,这两种产物在十二烷基硫酸钠 - 聚丙烯酰胺凝胶上与病毒粒子多肽X迁移率相同。我们的数据表明,羧基末端48个残基片段的进一步切割产生了一个19个氨基酸的片段,其氨基酸组成与μ相同(K. 细川和M. T. 宋,《病毒学杂志》17:924 - 934,1976年)。