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腺病毒12型感染和转化细胞中早期病毒基因产物的表达。

Expression of early viral gene products in adenovirus type 12-infected and -transformed cells.

作者信息

Esche H, Siegmann B

出版信息

J Gen Virol. 1982 May;60(Pt 1):99-113. doi: 10.1099/0022-1317-60-1-99.

Abstract

We have analysed early viral gene products expressed in adenovirus type 12 (Ad12)-infected cells as well as in two Ad12-transformed hamster cell lines, and Ad12-induced rat tumour cell lines by cell-free translation of virus-specific RNA which was selected by hybridization to cloned restriction endonuclease fragments of virus DNA. Proteins synthesized in vitro were analysed by one- and two-dimensional gel electrophoresis. It was found that RNA encoded by early region E1A directs the synthesis of at least eight polypeptides with apparent mol. wt. 38K, 36K, 30K, 28K, 26K, 25K, 24K and 22K. All these proteins are related to each other. E1B-specific RNA directs the synthesis of three proteins: 59K, 19K and 17K. Early region E2a codes for a 61K polypeptide which probably represents the single-strand DNA-binding protein of Ad12. RNA complementary to region E3 directs the synthesis of a 16K protein, and RNA transcribed from region E4 the synthesis of polypeptides with mol. wt. 20K, 18K and 11.5K. We have mapped a 67K polypeptide into the region within 11 to 28 map units (E2b). The analysis of proteins directed by virus-specific RNAs prepared from two Ad12-transformed hamster cell lines (T637, HA12/7) and one Ad12-induced rat tumour line (RBT12/3) showed that early regions E1 and E4 are expressed in all three Ad12-transformed cell lines. RNA transcribed from early regions E2 and E3 have been detected in lines T637 and RBT12/3. The virus RNA prepared from the Ad12-transformed cell lines directed synthesis of polypeptides with mol. wt. very similar to those of early virus proteins from infected cells. However, in all three Ad12-transformed cell lines mentioned above we have found RNAs which directed the synthesis of additional polypeptides of early regions E1 (34K) and E4 (25K, 24K) not detected in infected cells. The DNA sequence between 11 and 28 map units (coding for the 67K protein) is not expressed in the Ad12-transformed cells.

摘要

我们通过对与病毒DNA克隆限制性内切酶片段杂交筛选出的病毒特异性RNA进行无细胞翻译,分析了在12型腺病毒(Ad12)感染的细胞、两种Ad12转化的仓鼠细胞系以及Ad12诱导的大鼠肿瘤细胞系中表达的早期病毒基因产物。通过一维和二维凝胶电泳分析体外合成的蛋白质。发现早期区域E1A编码的RNA指导合成至少8种表观分子量分别为38K、36K、30K、28K、26K、25K、24K和22K的多肽。所有这些蛋白质相互关联。E1B特异性RNA指导合成三种蛋白质:59K、19K和17K。早期区域E2a编码一种61K的多肽,可能代表Ad12的单链DNA结合蛋白。与E3区域互补的RNA指导合成一种16K的蛋白质,从E4区域转录的RNA指导合成分子量分别为20K、18K和11.5K的多肽。我们已将一种67K的多肽定位到11至28个图距单位(E2b)内的区域。对从两种Ad12转化的仓鼠细胞系(T637、HA12/7)和一种Ad12诱导的大鼠肿瘤细胞系(RBT12/3)制备的病毒特异性RNA所指导的蛋白质分析表明,早期区域E1和E4在所有三种Ad12转化的细胞系中均有表达。在T637和RBT12/3细胞系中检测到了从早期区域E2和E3转录的RNA。从Ad12转化的细胞系制备的病毒RNA指导合成的多肽分子量与感染细胞中早期病毒蛋白的分子量非常相似。然而,在上述所有三种Ad12转化的细胞系中,我们发现了一些RNA,它们指导合成感染细胞中未检测到的早期区域E1(34K)和E4(25K、24K)的额外多肽。11至28个图距单位之间的DNA序列(编码67K蛋白质)在Ad12转化的细胞中不表达。

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