Halbert D N, Spector D J, Raskas H J
J Virol. 1979 Sep;31(3):621-9. doi: 10.1128/JVI.31.3.621-629.1979.
Region 1 DNA sequences (map positions 0 to 11% on the linear adenovirus 2 genome) are expressed both early and late in lytic infection and are required for transformation by the virus. During productive infection six distinct cytoplasmic RNAs are synthesized from this region. These RNAs comprise two families, each consisting of three size classes that share 3' sequences. Region 1 RNA's were purified by hybridization selection, using restriction fragments bound to nitrocellulose membranes, and by size fractionation. The isolated RNAs were then translated in cell-free systems derived from wheat germ and rabbit reticulocytes. The family of RNAs specified by 0 to 4.4 sequences includes two RNAs, which are 12S and 13S in size. These RNAs were partially separated by molecular weight and translated. The 13S RNA produced 53,000-dalton (53K) and 41K peptides, and the 12S RNA synthesized 47K and 35K products. The family of RNAs mapping from 4.4 to 11.0 encodes three separate polypeptides, each of which can be assigned to a specific RNA. A 12K product that comigrates with structural polypeptide IX is synthesized from the 9S RNA as previously reported (U. Pettersson and M. B. Mathews, Cell 12:741-750, 1977). The 13S RNA encodes a 15K polypeptide that corresponds to a 15K polypeptide in infected cell extracts. The 22s RNA encodes a 52K protein distinct from the 0 to 4.4 polypeptides.
1区DNA序列(在线性腺病毒2基因组上的图谱位置为0至11%)在裂解感染的早期和晚期均有表达,并且是病毒转化所必需的。在增殖性感染期间,从该区域合成了六种不同的细胞质RNA。这些RNA组成两个家族,每个家族由三个共享3'序列的大小类别组成。1区RNA通过杂交筛选进行纯化,使用与硝酸纤维素膜结合的限制性片段,并通过大小分级分离。然后将分离的RNA在源自小麦胚芽和兔网织红细胞的无细胞系统中进行翻译。由0至4.4序列指定的RNA家族包括两种RNA,其大小分别为12S和13S。这些RNA通过分子量进行部分分离并进行翻译。13S RNA产生53,000道尔顿(53K)和41K的肽,12S RNA合成47K和35K的产物。定位在4.4至11.0的RNA家族编码三种不同的多肽,每种多肽都可以指定到一种特定的RNA。如先前报道(U. Pettersson和M. B. Mathews,《细胞》12:741 - 750,1977),从9S RNA合成了一种与结构多肽IX共迁移的12K产物。13S RNA编码一种15K的多肽,该多肽与感染细胞提取物中的一种15K多肽相对应。22S RNA编码一种与0至4.4多肽不同的52K蛋白质。