Westin E H, Gorse K M, Clarke M F
Department of Medicine, Medical College of Virginia, Virginia Commonwealth University.
Oncogene. 1990 Aug;5(8):1117-24.
Two cDNA clones of the human c-myb gene have been isolated from a CCRF-CEM leukemia cell cDNA library and sequenced in their entirety. These sequences, when compared with those previously reported for the human c-myb gene, reveal an alternative splicing process that generates at least four forms of the c-myb message. Three of these forms co-migrate on Northern blots and are co-expressed in several human hematopoietic cell types. Data on sequence comparisons with mouse and chicken homologues of c-myb coupled with oligonucleotide hybridization to genomic clones of the human c-myb gene indicate that this alternative splicing process utilizes three closely spaced splice donor sites and two unique exons present between viral defined exons 5 and 6. In one clone, the alternative splicing would generate a predicted myb protein with a three amino acid deletion in the region involved in transcription activation. In the other clone, incorporation of a new exon leads to introduction of a translation stop codon leading to loss of the entire carboxy terminus of the protein. This includes loss of a portion of the region involved in transcription activation as well as a separate highly conserved domain. The effect of these changes on protein function is currently unknown.
已从CCRF - CEM白血病细胞cDNA文库中分离出两个人类c - myb基因的cDNA克隆,并对其进行了全序列测定。将这些序列与先前报道的人类c - myb基因序列进行比较时,发现了一种可变剪接过程,该过程产生至少四种形式的c - myb信使RNA。其中三种形式在Northern印迹上共迁移,并在几种人类造血细胞类型中共同表达。与c - myb的小鼠和鸡同源物的序列比较数据,以及与人c - myb基因基因组克隆的寡核苷酸杂交表明,这种可变剪接过程利用了三个紧密相邻的剪接供体位点和病毒定义的外显子5和6之间存在的两个独特外显子。在一个克隆中,可变剪接将产生一种预测的myb蛋白,该蛋白在参与转录激活的区域有三个氨基酸缺失。在另一个克隆中,一个新外显子的掺入导致引入一个翻译终止密码子,导致蛋白质整个羧基末端的缺失。这包括参与转录激活的区域的一部分以及一个单独的高度保守结构域的缺失。这些变化对蛋白质功能的影响目前尚不清楚。