539 related articles for article (PubMed ID: 25641578)
1. Nuclear localization domains of GATA activator Gln3 are required for transcription of target genes through dephosphorylation in Saccharomyces cerevisiae.
Numamoto M; Tagami S; Ueda Y; Imabeppu Y; Sasano Y; Sugiyama M; Maekawa H; Harashima S
J Biosci Bioeng; 2015 Aug; 120(2):121-7. PubMed ID: 25641578
[TBL] [Abstract][Full Text] [Related]
2. More than One Way in: Three Gln3 Sequences Required To Relieve Negative Ure2 Regulation and Support Nuclear Gln3 Import in
Tate JJ; Rai R; Cooper TG
Genetics; 2018 Jan; 208(1):207-227. PubMed ID: 29113979
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Nuclear Gln3 Import Is Regulated by Nitrogen Catabolite Repression Whereas Export Is Specifically Regulated by Glutamine.
Rai R; Tate JJ; Shanmuganatham K; Howe MM; Nelson D; Cooper TG
Genetics; 2015 Nov; 201(3):989-1016. PubMed ID: 26333687
[TBL] [Abstract][Full Text] [Related]
5. Tor pathway control of the nitrogen-responsive DAL5 gene bifurcates at the level of Gln3 and Gat1 regulation in Saccharomyces cerevisiae.
Georis I; Tate JJ; Cooper TG; Dubois E
J Biol Chem; 2008 Apr; 283(14):8919-29. PubMed ID: 18245087
[TBL] [Abstract][Full Text] [Related]
6. General Amino Acid Control and 14-3-3 Proteins Bmh1/2 Are Required for Nitrogen Catabolite Repression-Sensitive Regulation of Gln3 and Gat1 Localization.
Tate JJ; Buford D; Rai R; Cooper TG
Genetics; 2017 Feb; 205(2):633-655. PubMed ID: 28007891
[TBL] [Abstract][Full Text] [Related]
7. Nitrogen starvation and TorC1 inhibition differentially affect nuclear localization of the Gln3 and Gat1 transcription factors through the rare glutamine tRNACUG in Saccharomyces cerevisiae.
Tate JJ; Rai R; Cooper TG
Genetics; 2015 Feb; 199(2):455-74. PubMed ID: 25527290
[TBL] [Abstract][Full Text] [Related]
8. A domain in the transcription activator Gln3 specifically required for rapamycin responsiveness.
Rai R; Tate JJ; Shanmuganatham K; Howe MM; Cooper TG
J Biol Chem; 2014 Jul; 289(27):18999-9018. PubMed ID: 24847055
[TBL] [Abstract][Full Text] [Related]
9. Distinct phosphatase requirements and GATA factor responses to nitrogen catabolite repression and rapamycin treatment in Saccharomyces cerevisiae.
Tate JJ; Georis I; Dubois E; Cooper TG
J Biol Chem; 2010 Jun; 285(23):17880-95. PubMed ID: 20378536
[TBL] [Abstract][Full Text] [Related]
10. gln3 mutations dissociate responses to nitrogen limitation (nitrogen catabolite repression) and rapamycin inhibition of TorC1.
Rai R; Tate JJ; Nelson DR; Cooper TG
J Biol Chem; 2013 Jan; 288(4):2789-804. PubMed ID: 23223232
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Rapamycin-induced Gln3 dephosphorylation is insufficient for nuclear localization: Sit4 and PP2A phosphatases are regulated and function differently.
Tate JJ; Georis I; Feller A; Dubois E; Cooper TG
J Biol Chem; 2009 Jan; 284(4):2522-34. PubMed ID: 19015262
[TBL] [Abstract][Full Text] [Related]
13. Cytoplasmic compartmentation of Gln3 during nitrogen catabolite repression and the mechanism of its nuclear localization during carbon starvation in Saccharomyces cerevisiae.
Cox KH; Tate JJ; Cooper TG
J Biol Chem; 2002 Oct; 277(40):37559-66. PubMed ID: 12140287
[TBL] [Abstract][Full Text] [Related]
14. GATA Factor Regulation in Excess Nitrogen Occurs Independently of Gtr-Ego Complex-Dependent TorC1 Activation.
Tate JJ; Georis I; Rai R; Vierendeels F; Dubois E; Cooper TG
G3 (Bethesda); 2015 May; 5(8):1625-38. PubMed ID: 26024867
[TBL] [Abstract][Full Text] [Related]
15. Stress-responsive Gln3 localization in Saccharomyces cerevisiae is separable from and can overwhelm nitrogen source regulation.
Tate JJ; Cooper TG
J Biol Chem; 2007 Jun; 282(25):18467-18480. PubMed ID: 17439949
[TBL] [Abstract][Full Text] [Related]
16. N- and C-terminal Gln3-Tor1 interaction sites: one acting negatively and the other positively to regulate nuclear Gln3 localization.
Tate JJ; Rai R; De Virgilio C; Cooper TG
Genetics; 2021 Apr; 217(4):. PubMed ID: 33857304
[TBL] [Abstract][Full Text] [Related]
17. Nitrogen-responsive regulation of GATA protein family activators Gln3 and Gat1 occurs by two distinct pathways, one inhibited by rapamycin and the other by methionine sulfoximine.
Georis I; Tate JJ; Cooper TG; Dubois E
J Biol Chem; 2011 Dec; 286(52):44897-912. PubMed ID: 22039046
[TBL] [Abstract][Full Text] [Related]
18. Differing responses of Gat1 and Gln3 phosphorylation and localization to rapamycin and methionine sulfoximine treatment in Saccharomyces cerevisiae.
Kulkarni A; Buford TD; Rai R; Cooper TG
FEMS Yeast Res; 2006 Mar; 6(2):218-29. PubMed ID: 16487345
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Actin cytoskeleton is required for nuclear accumulation of Gln3 in response to nitrogen limitation but not rapamycin treatment in Saccharomyces cerevisiae.
Cox KH; Tate JJ; Cooper TG
J Biol Chem; 2004 Apr; 279(18):19294-301. PubMed ID: 14970238
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
