Activated Drosophila Ras1 is selectively suppressed by isoprenyl transferase inhibitors

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 wit...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1995-11, Vol.92 (24), p.10919-10923
Hauptverfasser: Kauffmann, R.C. (University of Pittsburgh, Pittsburgh, PA.), Qian, Y, Vogt, A, Sebti, S.M, Hamilton, A.D, Carthew, R.W
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Sprache:eng
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Zusammenfassung: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 wholeanimal model system
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.92.24.10919