ACTIVATED DROSOPHILA RAS1 IS SELECTIVELY SUPPRESSED BY ISOPRENYL TRANSFERASE INHIBITORS

被引:28
作者
KAUFFMANN, RC
QIAN, Y
VOGT, A
SEBTI, SM
HAMILTON, AD
CARTHEW, RW
机构
[1] UNIV PITTSBURGH,DEPT BIOL SCI,PITTSBURGH,PA 15260
[2] UNIV PITTSBURGH,DEPT CHEM,PITTSBURGH,PA 15260
[3] UNIV PITTSBURGH,DEPT PHARMACOL,PITTSBURGH,PA 15260
关键词
D O I
10.1073/pnas.92.24.10919
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ras CAAX (C = cysteine, A = aliphatic amino acid, and X = any amino acid) peptidomimetic inhibitors of farnesyl protein transferase suppress Ras-dependent cell transformation by preventing farnesylation of the Ras oncoprotein. These compounds are potential anticancer agents for tumors associated with Ras mutations. The peptidomimetic FTI-254 was tested for Ras1-inhibiting activity in whole animals by injection of activated Ras1(val12) Drosophila larvae. FTI-254 decreased the ability of Ras1(val12) to form supernumerary R7 photoreceptor cells in the compound eye of transformed flies. In contrast, it had no effect on the related supernumerary R7 phenotypes of flies transformed with either the activated sevenless receptor tyrosine kinase, Raf kinase, or a chimeric Ras1(val12) protein that is membrane associated through myristylation instead of isoprenylation. Therefore, FTI-254 acts as an isoprenylation inhibitor to selectively inhibit Ras1(val12) signaling activity in a whole-animal model system.
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页码:10919 / 10923
页数:5
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