Yeast Gcn4p stabilization is initiated by the dissociation of the nuclear Pho85p/Pcl5p complex

Katrin Bömeke, Ralph Pries, Virginia Korte, Eva Scholz, Britta Herzog, Florian Schulze, Gerhard H. Braus*

*Corresponding author for this work
19 Citations (Scopus)


Protein stability of the c-jun-like yeast bZIP transcriptional activator Gcn4p is exclusively controlled in the yeast nucleus. Phosphorylation by the nuclear Pho85p cyclin-dependent protein kinase, a functional homolog of mammalian Cdk5, initiates the Gcn4p degradation pathway in complex with the cyclin Pcl5p. We show that the initial step in Gcn4p stabilization is the dissociation of the Pho85p/Pcl5p complex. Pcl7p, another nuclear and constantly present cyclin, is required for Gcn4p stabilization and is able to associate to Pho85p independently of the activity of the Gcn4p degradation pathway. In addition, the nuclear cyclin-dependent Pho85p kinase inhibitor Pho81p is required for Gcn4p stabilization. Pho81p only interacts with Pcl5p when Gcn4p is rapidly degraded but constitutively interacts with Pcl7p. Our data suggest that Pcl7p and Pho81p are antagonists of the Pho85p/Pcl5p complex formation in a yet unknown way, which are specifically required for Gcn4p stabilization. We suggest that dissociation of the Pho85p/Pcl5p complex as initial step in Gcn4p stabilization is a prerequisite for a shift of equilibrium to an increased amount of the Pho85p/Pcl7p complexes and subsequently results in decreased Gcn4p phosphorylation and therefore increased stability of the transcription factor.

Original languageEnglish
JournalMolecular Biology of the Cell
Issue number7
Pages (from-to)2952-2962
Number of pages11
Publication statusPublished - 07.2006


Dive into the research topics of 'Yeast Gcn4p stabilization is initiated by the dissociation of the nuclear Pho85p/Pcl5p complex'. Together they form a unique fingerprint.

Cite this