Prywes R, Foulkes J G, Baltimore D
J Virol. 1985 Apr;54(1):114-22. doi: 10.1128/JVI.54.1.114-122.1985.
Only 1.2 kilobases (kb) at the 5' end of the 3.9-kb v-abl sequence in Abelson murine leukemia virus is required for fibroblast transformation. A precise delineation of this minimum transforming region was made by using small 5' or 3' deletions. Insertions of four amino acids, generated by putting synthetic DNA linkers into various restriction enzyme cleavage sites, abolished transforming activity, indicating that much of the internal sequence of the minimum transforming region plays a critical role in the transformation process. This 5' 1.2 kb of v-abl encodes protein-tyrosine kinase activity when expressed in Escherichia coli. Each of the mutations which caused a loss of transformation activity also resulted in a loss of protein-tyrosine kinase activity when expressed in E. coli. The minimum transforming region of v-abl contains amino acid homology to other protein-tyrosine kinase oncogenes, and a comparison with these oncogenes is presented.
艾贝尔森鼠白血病病毒中3.9千碱基(kb)的v-abl序列5'端仅1.2千碱基对于成纤维细胞转化是必需的。通过使用小的5'或3'缺失对这个最小转化区域进行了精确界定。通过将合成DNA接头插入各种限制酶切割位点产生的四个氨基酸的插入消除了转化活性,这表明最小转化区域的大部分内部序列在转化过程中起关键作用。当在大肠杆菌中表达时,v-abl的这5' 1.2 kb编码蛋白酪氨酸激酶活性。在大肠杆菌中表达时,每个导致转化活性丧失的突变也导致蛋白酪氨酸激酶活性丧失。v-abl的最小转化区域与其他蛋白酪氨酸激酶癌基因存在氨基酸同源性,并对这些癌基因进行了比较。