This is an archive of papers published by the staff and faculty of Fox Chase Cancer Center. For questions about content, please contact Talbot Research Library
Last updated on
van Slegtenhorst M , Carr E , Stoyanova R , Kruger WD , Henske EP
Tsc1(+) and tsc2(+) regulate arginine uptake and metabolism in Schizosaccharomyces pombe
Journal of Biological Chemistry. 2004 Mar;279(13) :12706-12713
AbstractMutations in either TSC1 or TSC2 cause tuberous sclerosis complex, an autosomal dominant disorder characterized by seizures, mental retardation, and benign tumors of the skin, brain, heart, and kidneys. Homologs for the TSC1 and TSC2 genes have been identified in mouse, rat, Fugu, Drosophila, and in the yeast Schizosaccharomyces pombe. Here we show that S. pombe lacking tsc1(+) or tsc2(+) have similar phenotypes including decreased arginine uptake, decreased expression of three amino acid permeases, and low intracellular levels of four members of the arginine biosynthesis pathway. Recently, the small GTPase Rheb was identified as a target of the GTPase-activating domain of tuberin in mammalian cells and in Drosophila. We show that the defect in arginine uptake in cells lacking tsc2(+) is rescued by the expression of a dominant negative form of rhb1(+), the Rheb homolog in S. pombe, but not by expressing wildtype rhb1(+). Expression of the tsc2(+) gene with a patient-derived ! mutation within the GAP domain did not rescue the arginine uptake defect in tsc2(+) mutant yeast. Taken together, these findings support a model in which arginine uptake is regulated through tsc1(+), tsc2(+), and rhb1(+) in S. pombe and also suggest a role for the Tsc1 and Tsc2 proteins in amino acid biosynthesis and sensing.
NotesEnglish Article Life Sciences (LS) van Slegtenhorst, M; Fox Chase Canc Ctr, Dept Med Oncol, 333 Cottman Ave, Philadelphia, PA 19111 USA. 0021-9258