Document Detail

Fission yeast tor1 functions in response to various stresses including nitrogen starvation, high osmolarity, and high temperature.
MedLine Citation:
PMID:  11409178     Owner:  NLM     Status:  MEDLINE    
A target of rapamycin (TOR) protein is a protein kinase that exerts cellular signal transduction to regulate cell growth in response to extracellular nutrient conditions. In the Schizosaccharomyces pombe genome database, there are two genes encoding TOR-related proteins, but their functions have not been analyzed. Here we report that one of the genes, referred to as tor1+, is required for sexual development induced by nitrogen starvation. Ste11 is a key transcription factor for the initiation of sexual development. The expression of ste11+ is normally regulated in tor1- cells; and overexpression of ste11+ hardly rescues the defect in fertility in tor1-. Upon nitrogen starvation, tor1+ cells promote two rounds of the cell cycle to become arrested at the G1 phase before initiation of sexual development. The tor1- cells do not promote such a cell cycle, suggesting that Tor1 is necessary for the response to nitrogen starvation. The tor1- cells show no growth or very slow growth under various stress conditions, including external high pH, high concentrations of salts or sorbitol, and high temperature. These results suggest that Tor1 is necessary for any response to a wide range of stresses. The vegetative growth of tor1- cells is inhibited by rapamycin, although tor1+ cells are resistant to the drug. The tor1- cells are hypersensitive to fluphenazine and cyclosporin A, which specifically inhibit calmodulin and calcineurin, respectively.
M Kawai; A Nakashima; M Ueno; T Ushimaru; K Aiba; H Doi; M Uritani
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Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Current genetics     Volume:  39     ISSN:  0172-8083     ISO Abbreviation:  Curr. Genet.     Publication Date:  2001 May 
Date Detail:
Created Date:  2001-06-18     Completed Date:  2002-01-14     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  8004904     Medline TA:  Curr Genet     Country:  United States    
Other Details:
Languages:  eng     Pagination:  166-74     Citation Subset:  IM    
Department of Chemistry, Faculty of Science, Shizuoka University, 836 Oya, Shizuoka, 422-8529, Japan.
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MeSH Terms
1-Phosphatidylinositol 3-Kinase*
Amino Acid Sequence
Calcium-Calmodulin-Dependent Protein Kinases / genetics,  metabolism
Cell Differentiation
Cloning, Molecular
Conserved Sequence
Fungal Proteins* / genetics*,  physiology
Gene Expression Regulation, Fungal
Genes, Fungal
Hydrogen-Ion Concentration
Molecular Sequence Data
Nitrogen / metabolism
Osmolar Concentration
Phosphotransferases (Alcohol Group Acceptor)* / genetics*
Saccharomyces cerevisiae / physiology
Saccharomyces cerevisiae Proteins*
Schizosaccharomyces / genetics*,  physiology*
Schizosaccharomyces pombe Proteins*
Sequence Homology, Amino Acid
Signal Transduction / genetics
Transcription Factors / physiology
Reg. No./Substance:
0/Fungal Proteins; 0/Saccharomyces cerevisiae Proteins; 0/Schizosaccharomyces pombe Proteins; 0/Transcription Factors; 145139-18-0/ste11 protein, S pombe; 7727-37-9/Nitrogen; EC 2.7.1.-/Phosphotransferases (Alcohol Group Acceptor); EC 3-Kinase; EC protein, S cerevisiae; EC Protein Kinases

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