Ceci J D, Patriotis C P, Tsatsanis C, Makris A M, Kovatch R, Swing D A, Jenkins N A, Tsichlis P N, Copeland N G
National Cancer Institute-Frederick Cancer Research Facility and Development Center, Maryland 21702, USA.
Genes Dev. 1997 Mar 15;11(6):688-700. doi: 10.1101/gad.11.6.688.
Provirus insertion in the last intron of the Tpl-2 gene in retrovirus-induced rat T-cell lymphomas results in the enhanced expression of a carboxy-terminally truncated Tpl-2 kinase. Here we show that the truncated protein exhibits an approximately sevenfold higher catalytic activity and is two- to threefold more efficient in activating the MAPK and SAPK pathways relative to the wild-type protein. The truncated Tpl-2 protein and a GST fusion of the Tpl-2 carboxy-terminal tail interact when coexpressed in Sf9 cells. Their interaction down-regulates the kinase activity of the truncated protein suggesting that tail-directed intramolecular interactions regulate the Tpl-2 kinase. Tpl-2 transgenic mice expressing the wild-type protein from the proximal Lck promoter fail to show a biological phenotype, whereas mice expressing the truncated protein develop large-cell lymphoblastic lymphomas of T-cell origin. These results show that Tpl-2 is an oncogenic kinase that is activated by carboxy-terminal truncation.
逆转录病毒诱导的大鼠T细胞淋巴瘤中,前病毒插入Tpl-2基因的最后一个内含子导致羧基末端截短的Tpl-2激酶表达增强。我们在此表明,截短的蛋白表现出约七倍高的催化活性,相对于野生型蛋白,在激活MAPK和SAPK途径方面效率高出两到三倍。截短的Tpl-2蛋白与Tpl-2羧基末端尾巴的GST融合蛋白在Sf9细胞中共表达时会相互作用。它们的相互作用下调了截短蛋白的激酶活性,表明尾巴导向的分子内相互作用调节Tpl-2激酶。从近端Lck启动子表达野生型蛋白的Tpl-2转基因小鼠未表现出生物学表型,而表达截短蛋白的小鼠则发生T细胞起源的大细胞淋巴母细胞淋巴瘤。这些结果表明,Tpl-2是一种通过羧基末端截短而激活的致癌激酶。