Fission Yeast TORC2 Signaling Pathway Ensures Cell Proliferation under Glucose-Limited, Nitrogen-Replete Conditions

被引:7
|
作者
Toyoda, Yusuke [1 ]
Saitoh, Shigeaki [1 ]
机构
[1] Kurume Univ, Inst Life Sci, Asahi Machi 67, Kurume, Fukuoka 8300011, Japan
基金
日本学术振兴会;
关键词
glucose limitation; nitrogen starvation; hexose transporter; TORC2; arrestin; ubiquitylation; endocytosis; Gad8/AKT kinase; PHOSPHODIESTERASE ACTIVATION; STARVATION; PROTEIN; KINASE; TRANSPORTER; TXNIP; TRANSLOCATION; THIOREDOXIN; REGULATOR; ARRESTIN;
D O I
10.3390/biom11101465
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
Target of rapamycin (TOR) kinases form two distinct complexes, TORC1 and TORC2, which are evolutionarily conserved among eukaryotes. These complexes control intracellular biochemical processes in response to changes in extracellular nutrient conditions. Previous studies using the fission yeast, Schizosaccharomyces pombe, showed that the TORC2 signaling pathway, which is essential for cell proliferation under glucose-limited conditions, ensures cell-surface localization of a high-affinity hexose transporter, Ght5, by downregulating its endocytosis. The TORC2 signaling pathway retains Ght5 on the cell surface, depending on the presence of nitrogen sources in medium. Ght5 is transported to vacuoles upon nitrogen starvation. In this review, we discuss the molecular mechanisms underlying this regulation to cope with nutritional stress, a response which may be conserved from yeasts to mammals.</p>
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页数:8
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