Aleström P, Akusjärvi G, Pettersson M, Pettersson U
J Biol Chem. 1982 Nov 25;257(22):13492-8.
We have determined the complete nucleotide sequence of a 5783-base pair segment of adenovirus type 2 DNA, located between map coordinates 15.8 and 31.7. This region of the adenovirus-2 genome encodes the three segments of the tripartite leader, the i-leader and the two species of virus-associated RNA. The established sequence reveals two translational reading frames encoded by the viral 1-strand which have remarkably large coding capacities. One of these is located between map coordinates 28.9 and 23.5 and encodes a hypothetical polypeptide with an estimated Mr = 74,000. This polypeptide is in an accompanying paper (Smart, J. E., and Stillman, B. W. (1982) J. Biol. Chem. 257, 13499-13506) identified as the precursor for the terminal protein which is covalently attached to the ends of adenovirus DNA. The second large open translational reading frame starts with an ATG triplet at coordinate 22.9 and encodes a hypothetical polypeptide with a predicted Mr = 120,400. This polypeptide is most likely the product of the N-gene, previously mapped between coordinates 18.0 and 22.5 (Galos, R. S., Williams, J., Binger, M. H., and Flint, S. J. (1979) Cell 17, 945-956). The sequence of the r-strand discloses several open translational reading frames, one of which is located within the i-leader.
我们已经确定了腺病毒2型DNA中一段5783个碱基对片段的完整核苷酸序列,该片段位于图谱坐标15.8和31.7之间。腺病毒2型基因组的这一区域编码了三联体前导序列的三个片段、i-前导序列以及两种病毒相关RNA。已确定的序列揭示了由病毒1链编码的两个翻译阅读框,它们具有显著大的编码能力。其中一个位于图谱坐标28.9和23.5之间,编码一种推测的多肽,估计分子量为74,000。在一篇随附论文中(斯马特,J.E.,和斯蒂尔曼,B.W.(1982年)《生物化学杂志》257,13499 - 13506),这种多肽被鉴定为末端蛋白的前体,该末端蛋白与腺病毒DNA的末端共价连接。第二个大的开放翻译阅读框从坐标22.9处的ATG三联体开始,编码一种推测的多肽,预测分子量为120,400。这种多肽很可能是N基因的产物,N基因先前被定位在坐标18.0和22.5之间(加洛斯,R.S.,威廉姆斯,J.,宾格,M.H.,和弗林特,S.J.(1979年)《细胞》17,945 - 956)。r链的序列揭示了几个开放翻译阅读框,其中一个位于i-前导序列内。