320 related articles for article (PubMed ID: 29113979)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Sit4 and PP2A Dephosphorylate Nitrogen Catabolite Repression-Sensitive Gln3 When TorC1 Is Up- as Well as Downregulated.
Tate JJ; Tolley EA; Cooper TG
Genetics; 2019 Aug; 212(4):1205-1225. PubMed ID: 31213504
[No Abstract] [Full Text] [Related]
10. 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]
11. 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]
12. Alterations in the Ure2 αCap domain elicit different GATA factor responses to rapamycin treatment and nitrogen limitation.
Feller A; Georis I; Tate JJ; Cooper TG; Dubois E
J Biol Chem; 2013 Jan; 288(3):1841-55. PubMed ID: 23184930
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
