Loss of ATP-dependent lysine uptake in the vacuolar membrane vesicles of Saccharomyces cerevisiae ypq1∆ mutant

References

• Yee DC, Shlykov MA, Vastermark A, Reddy VS, Arora S, Sun EI, Saier MH Jr. Characterization of amino acid pools in the vacuolar compartment of Saccharomyces cerevisiae. FEBS J. 2013;280:5780–5800.10.1111/febs.12499
   PubMed Web of Science ®Google Scholar
• Cherqui S, Kalatzis V, Trugnan G, Antignac C. The targeting of cystinosin to the lysosomal membrane requires a tyrosine-based signal and a novel sorting motif. J. Biol. Chem. 2001;276:13314–13321.10.1074/jbc.M010562200
   PubMed Web of Science ®Google Scholar
• Ruivo R, Bellenchi GC, Chen X, Zifarelli G, Sagne C, Debacker C, Pusch M, Supplisson S, Gasnier B. Mechanism of proton/substrate coupling in the heptahelical lysosomal transporter cystinosin. Proc. Nat. Acad. Sci. USA. 2012;109:210–217.10.1073/pnas.1115581109
   PubMed Web of Science ®Google Scholar
• Chung KS, Won M, Lee SB, Jang YJ, Hoe KL, Kim DU, Lee JW, Kim KW, Yoo HS. Isolation of a novel gene from Schizosaccharomyces pombe: stm1+ encoding a seven-transmembrane loop protein that may couple with the heterotrimeric Gα2 protein, Gpa2. J. Biol. Chem. 2001;276:40190–40201.
   PubMedGoogle Scholar
• Jézégou A, Llinares E, Anne C, Kieffer-Jaquinod S, O’Regan S, Aupetit J, Chabli A, Sagne C, Debacker C, Chadefaux-Vekemans B, Journet A, Andre B, Gasnier B. Heptahelical protein PQLC2 is a lysosomal cationic amino acid exporter underlying the action of cysteamine in cystinosis therapy. Proc. Nat. Acad. Sci. 2012;109:3434–3443.10.1073/pnas.1211198109
   PubMed Web of Science ®Google Scholar
• Sekito T, Chardwiriyapreecha S, Sugimoto N, Ishimoto M, Kawano-Kawada M, Kakinuma Y. Vacuolar transporter Avt4 is involved in excretion of basic amino acids from the vacuoles of Saccharomyces cerevisiae. Biosci. Biotechnol. Biochem. Forthcoming.
   Google Scholar
• Mumberg D, Muller R, Funk M. Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds. Gene. 1995;156:119–122.10.1016/0378-1119(95)00037-7
   PubMed Web of Science ®Google Scholar
• Ohsumi Y, Anraku Y. Active transport of basic amino acids driven by a proton motive force in vacuolar membrane vesicles of Saccharomyces cerevisiae. J. Biol. Chem. 1981;256:2079–2082.
   PubMed Web of Science ®Google Scholar
• Ohsumi Y, Anraku Y. Calcium transport driven by a proton motive force in vacuolar membrane vesicles of Saccharomyces cerevisiae. J. Biol. Chem. 1983;258:5614–5617.
   PubMed Web of Science ®Google Scholar
• Nishimura K, Igarashi K, Kakinuma Y. Proton gradient-driven nickel uptake by vacuolar membrane vesicles of Saccharomyces cerevisiae. J. Bacteriol. 1998;180:1962–1964.
   PubMed Web of Science ®Google Scholar
• Russnak R, Konczal D, McIntire SL. A family of yeast proteins mediating bidirectional vacuolar amino acid transport. J. Biol. Chem. 2001;276:23849–23857.10.1074/jbc.M008028200
   PubMed Web of Science ®Google Scholar
• Shimazu M, Sekito T, Akiyama K, Ohsumi Y, Kakinuma Y. A family of basic amino acid transporters of the vacuolar membrane from Saccharomyces cerevisiae. J. Biol. Chem. 2005;280:4851–4857.
   PubMed Web of Science ®Google Scholar
• Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 1951;193:265–275.
   PubMed Web of Science ®Google Scholar
• Kakinuma Y, Ohsumi Y, Anraku Y. Properties of H+-translocating adenosine triphosphatase in vacuolar membranes of Saccharomyces cerevisiae. J. Biol. Chem. 1981;256:10859–10863.
   PubMed Web of Science ®Google Scholar
• Chardwiriyapreecha S, Shimazu M, Morita T, Sekito T, Akiyama K, Takegawa K, Kakinuma Y. Identification of the fnx1+ and fnx2+ genes for vacuolar amino acid transporters in Schizosaccharomyces pombe. FEBS Lett. 2008;582:2225–2230.10.1016/j.febslet.2008.05.017
   Google Scholar
• Chahomchuen T, Hondo K, Ohsaki M, Sekito T, Kakinuma Y. Evidence for Avt6 as a vacuolar exporter of acidic amino acids in Saccharomyces cerevisiae cells. J. Gen. Appl. Microbiol. 2009;55:409–417.10.2323/jgam.55.409
   PubMed Web of Science ®Google Scholar
• Stanbrough M, Magasanik B. Transcriptional and posttranslational regulation of the general amino acid permease of Saccharomyces cerevisiae. J. Bacteriol. 1995;177:94–102.
   PubMed Web of Science ®Google Scholar
• Merhi A, Andre B. Internal amino acids promote Gap1 permease ubiquitylation via TORC1/Npr1/14-3-3-dependent control of the Bul arrestin-like adaptors. Mol. Cell. Biol. 2012;32:4510–4522.10.1128/MCB.00463-12
   PubMed Web of Science ®Google Scholar
• Cox KH, Rai R, Distler M, Daugherty JR, Coffman JA, Cooper TG. Saccharomyces cerevisiae GATA sequences function as TATA elements during nitrogen catabolite repression and when Gln3p is excluded from the nucleus by overproduction of Ure2p. J. Biol. Chem. 2000;275:17611–17618.10.1074/jbc.M001648200
   PubMed Web of Science ®Google Scholar
• Lin CH, MacGurn JA, Chu T, Stefan CJ, Emr SD. Arrestin-related ubiquitin-ligase adaptors regulate endocytosis and protein turnover at the cell surface. Cell. 2008;135:714–725.10.1016/j.cell.2008.09.025
   PubMed Web of Science ®Google Scholar