NPR1 kinase and RSP5-BUL1/2 ubiquitin ligase control GLN3-dependent transcription in Saccharomyces cerevisiae

被引:43
作者
Crespo, JL
Helliwell, SB
Wiederkehr, C
Demougin, P
Fowler, B
Primig, M
Hall, MN
机构
[1] Univ Basel, Div Biochem, CH-4056 Basel, Switzerland
[2] Univ Basel, Biozentrum, Swiss Inst Bioinformat, CH-4056 Basel, Switzerland
[3] Univ Childrens Hosp, CH-4005 Basel, Switzerland
关键词
D O I
10.1074/jbc.M407372200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The GATA transcription factors GLN3 and GAT1 activate nitrogen-regulated genes in Saccharomyces cerevisiae. NPR1 is a protein kinase that controls post-Golgi sorting of amino acid permeases. In the presence of a good nitrogen source, TOR ( target of rapamycin) maintains GLN3 and NPR1 phosphorylated and inactive by inhibiting the type 2A-related phosphatase SIT4. We identified NPR1 as a regulator of GLN3. Specifically, loss of NPR1 causes nuclear translocation and activation of GLN3, but not GAT1, in nitrogen-rich conditions. NPR1-mediated inhibition of GLN3 is independent of the phosphatase SIT4. We also demonstrate that the E3/E4 ubiquitin-protein ligase proteins RSP5 and BUL1/2 are required for GLN3 activation under poor nitrogen conditions. Thus, NPR1 and BUL1/2 antagonistically control GLN3-dependent transcription, suggesting a role for regulated ubiquitination in the control of nutrient-responsive transcription.
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页码:37512 / 37517
页数:6
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