Kaye F, Battey J, Nau M, Brooks B, Seifter E, De Greve J, Birrer M, Sausville E, Minna J
NCI-Navy Medical Oncology Branch, Naval Hospital, Bethesda, Maryland.
Mol Cell Biol. 1988 Jan;8(1):186-95. doi: 10.1128/mcb.8.1.186-195.1988.
We analyzed in detail the structure of the L-myc gene isolated from human placental DNA and characterized its expression in several small-cell lung cancer cell lines. The gene is composed of three exons and two introns spanning 6.6 kilobases in human DNA. Several distinct mRNA species are produced in all small-cell lung cancer cell lines that express L-myc. These transcripts are generated from a single gene by alternative splicing of introns 1 and 2 and by use of alternative polyadenylation signals. In some mRNAs there is a long open reading frame with a predicted translated protein of 364 residues. Amino acid sequence comparison with c-myc and N-myc demonstrated multiple discrete regions with extensive homology. In contrast, other mRNA transcripts, generated by alternative processing, could encode a truncated protein with a novel carboxy-terminal end.
我们详细分析了从人胎盘DNA中分离出的L-myc基因的结构,并对其在几种小细胞肺癌细胞系中的表达进行了表征。该基因由三个外显子和两个内含子组成,在人类DNA中跨度为6.6千碱基。在所有表达L-myc的小细胞肺癌细胞系中都产生了几种不同的mRNA种类。这些转录本是由单个基因通过内含子1和2的可变剪接以及使用可变聚腺苷酸化信号产生的。在一些mRNA中,有一个长的开放阅读框,预测翻译的蛋白质有364个残基。与c-myc和N-myc的氨基酸序列比较显示出多个具有广泛同源性的离散区域。相比之下,通过可变加工产生的其他mRNA转录本可以编码一种具有新的羧基末端的截短蛋白。