Nishimura T, Vogt P K
Department of Microbiology, University of Southern California, School of Medicine, Los Angeles 90033-1054.
Oncogene. 1988 Dec;3(6):659-63.
We have isolated chicken genomic and cDNA clones representing the jun oncogene of avian sarcoma virus 17 (ASV17). The genomic clone lacks intron sequences within its protein coding domain, contains a CAAT box, seven SP-1 consensus sequences and TATA box-like elements upstream and two poly(A) addition signals downstream of the coding domain. The cellular jun protein is 310 amino acids in length. Cellular and viral jun proteins differ by three nonconservative amino acid substitutions of which two are located in the DNA-binding domain, by a 27-amino-acid deletion in the amino terminal third of the viral jun protein, by eleven cell-coded amino acids that link the cellular jun coding domain to the viral gag domain and by the partial gag sequences constituting the amino terminal of the viral gag-jun fusion protein. The availability of a cellular jun cDNA now allows the construction of reciprocal recombinants between the viral and the cellular gene which will define the structural features required for the oncogenicity of v-jun.
我们已经分离出了代表禽肉瘤病毒17(ASV17)的jun癌基因的鸡基因组和cDNA克隆。该基因组克隆在其蛋白质编码域内缺乏内含子序列,在编码域上游含有一个CAAT框、七个SP-1共有序列和类似TATA框的元件,在编码域下游有两个聚腺苷酸化信号。细胞jun蛋白长度为310个氨基酸。细胞和病毒jun蛋白有三个非保守氨基酸取代不同,其中两个位于DNA结合域,病毒jun蛋白氨基末端三分之一处有27个氨基酸的缺失,有11个细胞编码的氨基酸将细胞jun编码域与病毒gag域相连,以及构成病毒gag-jun融合蛋白氨基末端的部分gag序列。细胞jun cDNA的可得性现在允许构建病毒基因和细胞基因之间的相互重组体,这将确定v-jun致癌性所需的结构特征。