RapamycinFungusV1, Main, Exploration, bibRecord, 001989

Convergence of TOR-nitrogen and Snf1-glucose signaling pathways onto Gln3.

Identifieur interne : 001989 ( Main/Exploration ); précédent : 001988; suivant : 001990

Convergence of TOR-nitrogen and Snf1-glucose signaling pathways onto Gln3.

Auteurs : Paula G. Bertram [États-Unis] ; Jae H. Choi ; John Carvalho ; Ting-Fung Chan ; Wandong Ai ; X F Steven Zheng

Source :

Molecular and cellular biology [ 0270-7306 ] ; 2002.

RBID : pubmed:11809814

Descripteurs français

KwdFr :
- Azote (métabolisme), Facteurs de transcription (métabolisme), Glucose (métabolisme), Gènes rapporteurs (MeSH), Phosphatidylinositol 3-kinases (MeSH), Phosphorylation (MeSH), Phosphotransferases (Alcohol Group Acceptor) (métabolisme), Protein-Serine-Threonine Kinases (métabolisme), Protéines de Saccharomyces cerevisiae (métabolisme), Protéines de fusion recombinantes (génétique), Protéines de fusion recombinantes (métabolisme), Protéines de liaison à l'ADN (métabolisme), Protéines de répression (MeSH), Protéines du cycle cellulaire (MeSH), Protéines fongiques (métabolisme), Saccharomyces cerevisiae (physiologie), Techniques de double hybride (MeSH), Transduction du signal (physiologie).
MESH :
- génétique : Protéines de fusion recombinantes.
- métabolisme : Azote, Facteurs de transcription, Glucose, Phosphotransferases (Alcohol Group Acceptor), Protein-Serine-Threonine Kinases, Protéines de Saccharomyces cerevisiae, Protéines de fusion recombinantes, Protéines de liaison à l'ADN, Protéines fongiques.
- physiologie : Saccharomyces cerevisiae, Transduction du signal.
- Gènes rapporteurs, Phosphatidylinositol 3-kinases, Phosphorylation, Protéines de répression, Protéines du cycle cellulaire, Techniques de double hybride.

English descriptors

KwdEn :
- Cell Cycle Proteins (MeSH), DNA-Binding Proteins (metabolism), Fungal Proteins (metabolism), Genes, Reporter (MeSH), Glucose (metabolism), Nitrogen (metabolism), Phosphatidylinositol 3-Kinases (MeSH), Phosphorylation (MeSH), Phosphotransferases (Alcohol Group Acceptor) (metabolism), Protein-Serine-Threonine Kinases (metabolism), Recombinant Fusion Proteins (genetics), Recombinant Fusion Proteins (metabolism), Repressor Proteins (MeSH), Saccharomyces cerevisiae (physiology), Saccharomyces cerevisiae Proteins (metabolism), Signal Transduction (physiology), Transcription Factors (metabolism), Two-Hybrid System Techniques (MeSH).
MESH :
- chemical , genetics : Recombinant Fusion Proteins.
- chemical , metabolism : DNA-Binding Proteins, Fungal Proteins, Glucose, Nitrogen, Phosphotransferases (Alcohol Group Acceptor), Protein-Serine-Threonine Kinases, Recombinant Fusion Proteins, Saccharomyces cerevisiae Proteins, Transcription Factors.
- chemical : Cell Cycle Proteins, Phosphatidylinositol 3-Kinases, Repressor Proteins.
- physiology : Saccharomyces cerevisiae, Signal Transduction.
- Genes, Reporter, Phosphorylation, Two-Hybrid System Techniques.

Abstract

Carbon and nitrogen are two basic nutrient sources for cellular organisms. They supply precursors for energy metabolism and metabolic biosynthesis. In the yeast Saccharomyces cerevisiae, distinct sensing and signaling pathways have been described that regulate gene expression in response to the quality of carbon and nitrogen sources, respectively. Gln3 is a GATA-type transcription factor of nitrogen catabolite-repressible (NCR) genes. Previous observations indicate that the quality of nitrogen sources controls the phosphorylation and cytoplasmic retention of Gln3 via the target of rapamycin (TOR) protein. In this study, we show that glucose also regulates Gln3 phosphorylation and subcellular localization, which is mediated by Snf1, the yeast homolog of AMP-dependent protein kinase and a cytoplasmic glucose sensor. Our data show that glucose and nitrogen signaling pathways converge onto Gln3, which may be critical for both nutrient sensing and starvation responses.

DOI: 10.1128/mcb.22.4.1246-1252.2002
PubMed: 11809814
PubMed Central: PMC134645

Affiliations:

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 001993
to stream Main, to step Curation: 001993

Le document en format XML

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<front><div type="abstract" xml:lang="en">Carbon and nitrogen are two basic nutrient sources for cellular organisms. They supply precursors for energy metabolism and metabolic biosynthesis. In the yeast Saccharomyces cerevisiae, distinct sensing and signaling pathways have been described that regulate gene expression in response to the quality of carbon and nitrogen sources, respectively. Gln3 is a GATA-type transcription factor of nitrogen catabolite-repressible (NCR) genes. Previous observations indicate that the quality of nitrogen sources controls the phosphorylation and cytoplasmic retention of Gln3 via the target of rapamycin (TOR) protein. In this study, we show that glucose also regulates Gln3 phosphorylation and subcellular localization, which is mediated by Snf1, the yeast homolog of AMP-dependent protein kinase and a cytoplasmic glucose sensor. Our data show that glucose and nitrogen signaling pathways converge onto Gln3, which may be critical for both nutrient sensing and starvation responses.</div>
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	Serveur d'exploration sur la rapamycine et les champignons
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Convergence of TOR-nitrogen and Snf1-glucose signaling pathways onto Gln3.

Convergence of TOR-nitrogen and Snf1-glucose signaling pathways onto Gln3.

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