Brickell P M, Patel M
Department of Biochemistry, University College and Middlesex School of Medicine, London, UK.
Br J Cancer. 1988 Dec;58(6):704-9. doi: 10.1038/bjc.1988.294.
The c-fgr protooncogene is a member of the c-src family of tyrosine kinases. Expression of c-fgr was studied in a series of Epstein-Barr virus (EBV) negative Burkitt's lymphoma cell lines and their EBV-converted derivatives. Two transcripts, of 2.9 kb and 3.5 kb, were present at dramatically elevated levels following EBV-conversion. The structure of the c-fgr transcripts was studied by the isolation and nucleotide sequence analysis of cDNA clones. This indicated that the c-fgr protein encoded by the mature mRNA would contain 529 amino acids and have a molecular weight of approximately 58,000. The N-terminus of the predicted c-fgr protein has low amino acid homology with the N-termini of other members of this family of proteins, suggesting a cell specific function for the N-terminal domain. Analysis of the c-fgr cDNA clones also revealed the presence of alternative functional polyadenylation signals, although the use of these does not account for the size difference between the two major c-fgr transcripts.
c-fgr原癌基因是酪氨酸激酶c-src家族的成员。在一系列爱泼斯坦-巴尔病毒(EBV)阴性的伯基特淋巴瘤细胞系及其EBV转化衍生物中研究了c-fgr的表达。在EBV转化后,两种转录本,即2.9 kb和3.5 kb的转录本,以显著升高的水平存在。通过cDNA克隆的分离和核苷酸序列分析研究了c-fgr转录本的结构。这表明由成熟mRNA编码的c-fgr蛋白将包含529个氨基酸,分子量约为58,000。预测的c-fgr蛋白的N末端与该蛋白家族其他成员的N末端具有低氨基酸同源性,这表明N末端结构域具有细胞特异性功能。对c-fgr cDNA克隆的分析还揭示了存在替代性功能性聚腺苷酸化信号,尽管这些信号的使用并不能解释两个主要c-fgr转录本之间的大小差异。