Neckameyer W S, Shibuya M, Hsu M T, Wang L H
Mol Cell Biol. 1986 May;6(5):1478-86. doi: 10.1128/mcb.6.5.1478-1486.1986.
A recombinant DNA clone containing cellular sequences homologous to the transforming sequence, v-ros, of avian sarcoma virus UR2 was isolated from a chicken genomic DNA library. Heteroduplex mapping and nucleotide sequencing reveal that the v-ros sequences are distributed in nine exons ranging from 65 to 204 nucleotides on cellular ros (c-ros) DNA over a range of 11 kilobases. Comparison of the deduced amino acid sequences of c-ros and v-ros shows two differences: v-ros contains a three-amino-acid insertion within the hydrophobic domain presumed to be involved in membrane association, and (ii) the carboxyl 12 amino acids of v-ros are completely different from those of the deduced c-ros sequence. The deduced amino acid sequence of c-ros bears striking structural features similar to those of insulin and epidermal growth factor receptors, including the presumed hydrophobic membrane binding domain, amino acids flanking the domain, and the distance between the domain and the catalytic region of the kinase activity. The expression of c-ros appears to be under a very stringent control. When tissues at various stages of chicken development were analyzed, only kidney was found to contain a significant level of c-ros RNA. The level of c-ros RNA in kidney tissue is most abundant in 7- to 14-day-old chickens. Finally, nucleotide sequences of c-ros DNA and UR2-associated helper viral genome at regions corresponding to the gag ros recombination site suggest that the junction has been formed by RNA splicing.
从鸡基因组DNA文库中分离出一个重组DNA克隆,其含有与禽肉瘤病毒UR2的转化序列v-ros同源的细胞序列。异源双链图谱分析和核苷酸测序表明,v-ros序列分布在细胞ros(c-ros)DNA上11千碱基范围内的9个外显子中,外显子长度从65至204个核苷酸不等。对推导的c-ros和v-ros氨基酸序列进行比较,发现两个差异:(i)v-ros在推测参与膜结合的疏水结构域内有一个三氨基酸插入;(ii)v-ros的羧基端12个氨基酸与推导的c-ros序列完全不同。推导的c-ros氨基酸序列具有与胰岛素和表皮生长因子受体相似的显著结构特征,包括推测的疏水膜结合结构域、该结构域两侧的氨基酸以及该结构域与激酶活性催化区域之间的距离。c-ros的表达似乎受到非常严格的调控。当分析鸡发育不同阶段的组织时,仅发现肾脏含有显著水平的c-ros RNA。肾脏组织中c-ros RNA水平在7至14日龄的鸡中最为丰富。最后,c-ros DNA和UR2相关辅助病毒基因组在与gag-ros重组位点相对应区域的核苷酸序列表明,该连接点是通过RNA剪接形成的。