272 related articles for article (PubMed ID: 26333687)
21. Gln3 phosphorylation and intracellular localization in nutrient limitation and starvation differ from those generated by rapamycin inhibition of Tor1/2 in Saccharomyces cerevisiae.
Cox KH; Kulkarni A; Tate JJ; Cooper TG
J Biol Chem; 2004 Mar; 279(11):10270-8. PubMed ID: 14679193
[TBL] [Abstract][Full Text] [Related]
22. Transduction of the nitrogen signal activating Gln3-mediated transcription is independent of Npr1 kinase and Rsp5-Bul1/2 ubiquitin ligase in Saccharomyces cerevisiae.
Feller A; Boeckstaens M; Marini AM; Dubois E
J Biol Chem; 2006 Sep; 281(39):28546-54. PubMed ID: 16864574
[TBL] [Abstract][Full Text] [Related]
23. Saccharomyces cerevisiae Sit4 phosphatase is active irrespective of the nitrogen source provided, and Gln3 phosphorylation levels become nitrogen source-responsive in a sit4-deleted strain.
Tate JJ; Feller A; Dubois E; Cooper TG
J Biol Chem; 2006 Dec; 281(49):37980-92. PubMed ID: 17015442
[TBL] [Abstract][Full Text] [Related]
24. Multiple Targets on the Gln3 Transcription Activator Are Cumulatively Required for Control of Its Cytoplasmic Sequestration.
Rai R; Tate JJ; Cooper TG
G3 (Bethesda); 2016 May; 6(5):1391-408. PubMed ID: 26976442
[TBL] [Abstract][Full Text] [Related]
25. Methionine sulfoximine treatment and carbon starvation elicit Snf1-independent phosphorylation of the transcription activator Gln3 in Saccharomyces cerevisiae.
Tate JJ; Rai R; Cooper TG
J Biol Chem; 2005 Jul; 280(29):27195-204. PubMed ID: 15911613
[TBL] [Abstract][Full Text] [Related]
26. Identification of direct and indirect targets of the Gln3 and Gat1 activators by transcriptional profiling in response to nitrogen availability in the short and long term.
Scherens B; Feller A; Vierendeels F; Messenguy F; Dubois E
FEMS Yeast Res; 2006 Aug; 6(5):777-91. PubMed ID: 16879428
[TBL] [Abstract][Full Text] [Related]
27. Ammonia regulates VID30 expression and Vid30p function shifts nitrogen metabolism toward glutamate formation especially when Saccharomyces cerevisiae is grown in low concentrations of ammonia.
van der Merwe GK; Cooper TG; van Vuuren HJ
J Biol Chem; 2001 Aug; 276(31):28659-66. PubMed ID: 11356843
[TBL] [Abstract][Full Text] [Related]
28. Intranuclear function for protein phosphatase 2A: Pph21 and Pph22 are required for rapamycin-induced GATA factor binding to the DAL5 promoter in yeast.
Georis I; Tate JJ; Feller A; Cooper TG; Dubois E
Mol Cell Biol; 2011 Jan; 31(1):92-104. PubMed ID: 20974806
[TBL] [Abstract][Full Text] [Related]
29. The yeast GATA factor Gat1 occupies a central position in nitrogen catabolite repression-sensitive gene activation.
Georis I; Feller A; Vierendeels F; Dubois E
Mol Cell Biol; 2009 Jul; 29(13):3803-15. PubMed ID: 19380492
[TBL] [Abstract][Full Text] [Related]
30. Glutamine transport as a possible regulator of nitrogen catabolite repression in Saccharomyces cerevisiae.
Georis I; Fayyad-Kazan M; Zaremba E; Vierendeels F; Roovers M; Dubois E
Yeast; 2022 Sep; 39(9):493-507. PubMed ID: 35942513
[TBL] [Abstract][Full Text] [Related]
31. Components of Golgi-to-vacuole trafficking are required for nitrogen- and TORC1-responsive regulation of the yeast GATA factors.
Fayyadkazan M; Tate JJ; Vierendeels F; Cooper TG; Dubois E; Georis I
Microbiologyopen; 2014 Jun; 3(3):271-87. PubMed ID: 24644271
[TBL] [Abstract][Full Text] [Related]
32. Gln3-Gcn4 hybrid transcriptional activator determines catabolic and biosynthetic gene expression in the yeast Saccharomyces cerevisiae.
Hernández H; Aranda C; Riego L; González A
Biochem Biophys Res Commun; 2011 Jan; 404(3):859-64. PubMed ID: 21184740
[TBL] [Abstract][Full Text] [Related]
33. Formalin can alter the intracellular localization of some transcription factors in Saccharomyces cerevisiae.
Tate JJ; Cooper TG
FEMS Yeast Res; 2008 Dec; 8(8):1223-35. PubMed ID: 19054131
[TBL] [Abstract][Full Text] [Related]
34. Five conditions commonly used to down-regulate tor complex 1 generate different physiological situations exhibiting distinct requirements and outcomes.
Tate JJ; Cooper TG
J Biol Chem; 2013 Sep; 288(38):27243-27262. PubMed ID: 23935103
[TBL] [Abstract][Full Text] [Related]
35. Nuclear translocation of Gln3 in response to nutrient signals requires Golgi-to-endosome trafficking in Saccharomyces cerevisiae.
Puria R; Zurita-Martinez SA; Cardenas ME
Proc Natl Acad Sci U S A; 2008 May; 105(20):7194-9. PubMed ID: 18443284
[TBL] [Abstract][Full Text] [Related]
36. Nitrogen catabolite repression in Saccharomyces cerevisiae.
Hofman-Bang J
Mol Biotechnol; 1999 Aug; 12(1):35-73. PubMed ID: 10554772
[TBL] [Abstract][Full Text] [Related]
37. Nitrogen catabolite repression-sensitive transcription as a readout of Tor pathway regulation: the genetic background, reporter gene and GATA factor assayed determine the outcomes.
Georis I; Feller A; Tate JJ; Cooper TG; Dubois E
Genetics; 2009 Mar; 181(3):861-74. PubMed ID: 19104072
[TBL] [Abstract][Full Text] [Related]
38. Roles of URE2 and GLN3 in the proline utilization pathway in Saccharomyces cerevisiae.
Xu S; Falvey DA; Brandriss MC
Mol Cell Biol; 1995 Apr; 15(4):2321-30. PubMed ID: 7891726
[TBL] [Abstract][Full Text] [Related]
39. Transmitting the signal of excess nitrogen in Saccharomyces cerevisiae from the Tor proteins to the GATA factors: connecting the dots.
Cooper TG
FEMS Microbiol Rev; 2002 Aug; 26(3):223-38. PubMed ID: 12165425
[TBL] [Abstract][Full Text] [Related]
40. The TOR-controlled transcription activators GLN3, RTG1, and RTG3 are regulated in response to intracellular levels of glutamine.
Crespo JL; Powers T; Fowler B; Hall MN
Proc Natl Acad Sci U S A; 2002 May; 99(10):6784-9. PubMed ID: 11997479
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]