Complex Formation, Phosphorylation, and Localization of Protein Kinase A of Schizosaccharomyces pombe upon Glucose Starvation

Bioscience, Biotechnology, and Biochemistry Volume 75 Issue 8 Page 1456-1465 published_at 2011-08-23
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Title
Complex Formation, Phosphorylation, and Localization of Protein Kinase A of Schizosaccharomyces pombe upon Glucose Starvation
Creator
GUPTA Dipali Rani
PAUL Swapan Kumar
OOWATARI Yasuo
Source Title
Bioscience, Biotechnology, and Biochemistry
Volume 75
Issue 8
Start Page 1456
End Page 1465
Journal Identifire
ISSN 0916-8451
EISSN 1347-6947
Descriptions
Nine sam mutants that undergo sexual differentiation without requiring starvation in Schizosaccharomyces pombe were previously isolated. In this study, we identified a nonsense mutation on the pka1 locus in the sam6 mutant. pka1 encodes a catalytic subunit of protein kinase A (PKA). Replacement and overexpression of pka1 suppressed the KCl sensitivity and hyper-mating phenotype of sam6, confirming that sam6 is an allele of pka1. To characterize further the regulation of Pka1, we tested the physical interaction between Pka1 and Cgs1 (a regulatory subunit of PKA). Pka1 and Cgs1 physically interacted under glucose-limited conditions but not under glucose-rich conditions. In addition, the formation of a Pka1-Cgs1 complex was detected under glucose-limited conditions by Blue Native PAGE. Furthermore, the Pka1 protein was found to be phosphorylated under glucose-starved conditions, and at the same time its localization shifted from the nucleus towards the cytoplasm (mainly the vacuoles), suggesting a strong relationship among phosphorylation, complex formation, and the cytoplasmic distribution of Pka1.
Subjects
fission yeast ( Other)
Schizosaccharomyces pombe ( Other)
protein kinase A ( Other)
sexual differentiation ( Other)
Language
eng
Resource Type journal article
Publisher
Japan Society for Bioscience, Biotechnology, and Agrochemistry
Date of Issued 2011-08-23
Publish Type Accepted Manuscript
Access Rights open access
Relation
[DOI] 10.1271/bbb.110125