Jacob L, Opper M, Metzroth B, Phannavong B, Mechler B M
Cell. 1987 Jul 17;50(2):215-25. doi: 10.1016/0092-8674(87)90217-0.
We have previously cloned lethal(2)giant larvae, a tumor-suppressor gene of Drosophila that normally controls cell proliferation and/or differentiation in the optic centers of the brain and the imaginal discs. Here we describe the structure of the l(2)gl genes as determined by sequencing genomic and cDNA clones. The structure of the cDNAs indicates the use of alternative splicing, either in the 5' untranslated exons or in the 3' coding exons. Thus the gene encodes two putative proteins of 1161 and 708 amino acids, p127 and p78, respectively, differing at their C termini. A 3'-truncated l(2)gl transposon that leaves the coding sequence of p78 intact but deletes 141 residues of p127 was capable of suppressing tumor formation in l(2)gl-deficient animals. These results suggest that the putative p78 protein is effective in controlling cell proliferation and/or differentiation.
我们之前克隆了致死(2)巨大幼虫基因,它是果蝇的一个肿瘤抑制基因,通常控制大脑视中枢和成虫盘的细胞增殖和/或分化。在此我们描述通过对基因组和cDNA克隆进行测序所确定的l(2)gl基因的结构。cDNA的结构表明在5'非翻译外显子或3'编码外显子中存在选择性剪接。因此该基因分别编码两种推定的蛋白质,即1161个氨基酸的p127和708个氨基酸的p78,它们的C末端不同。一个3'端截短的l(2)gl转座子,其保留了p78的编码序列但缺失了p127的141个残基,能够抑制l(2)gl缺陷动物中的肿瘤形成。这些结果表明推定的p78蛋白在控制细胞增殖和/或分化方面是有效的。