Shtivelman E, Lifshitz B, Gale R P, Roe B A, Canaani E
Cell. 1986 Oct 24;47(2):277-84. doi: 10.1016/0092-8674(86)90450-2.
The primary structure of normal abl protein was determined by sequencing the coding region of its cDNA. abl contains two alternative 5' exons spliced to a common set of 3' exons to yield the two major abl RNA transcripts. These transcripts initiate in different promoter regions and give rise to proteins that vary in their N-termini. In the human cell line K562, abl is translocated from chromosome 9 to within the bcr gene on chromosome 22. Within the fused bcr-abl gene, abl exon II alternatively splices to two adjacent bcr exons. This phenomenon is seen in many patients with chronic myeloid leukemia.
通过对正常abl蛋白cDNA编码区进行测序,确定了其一级结构。abl含有两个可变的5'外显子,它们与一组共同的3'外显子拼接,产生两种主要的abl RNA转录本。这些转录本在不同的启动子区域起始,并产生N端不同的蛋白质。在人细胞系K562中,abl从9号染色体易位至22号染色体上的bcr基因内。在融合的bcr-abl基因中,abl外显子II可选择性地与两个相邻的bcr外显子拼接。这种现象在许多慢性髓性白血病患者中都可见到。