TOR Complex 1: Orchestrating Nutrient Signaling and Cell Cycle Progression

被引:2
作者
Foltman, Magdalena [1 ,2 ]
Sanchez-Diaz, Alberto [1 ,2 ]
机构
[1] Univ Cantabria, CSIC, Inst Biomed & Biotecnol Cantabria IBBTEC, Mech & Regulat Cell Div,Res Unit, Santander 39011, Spain
[2] Univ Cantabria, Fac Med, Dept Biol Mol, Santander 39011, Spain
关键词
cell cycle; cell growth; TOR; TORC1; S; cerevisiae; budding yeast; PROTEIN-KINASE-A; SENSITIVE PHOSPHOPROTEOME REVEALS; CDK INHIBITOR SIC1; SACCHAROMYCES-CEREVISIAE; MESSENGER-RNA; GENE-EXPRESSION; RAPAMYCIN TOR; SIZE CONTROL; SUBSTRATE PHOSPHORYLATION; MULTISITE PHOSPHORYLATION;
D O I
10.3390/ijms242115745
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
The highly conserved TOR signaling pathway is crucial for coordinating cellular growth with the cell cycle machinery in eukaryotes. One of the two TOR complexes in budding yeast, TORC1, integrates environmental cues and promotes cell growth. While cells grow, they need to copy their chromosomes, segregate them in mitosis, divide all their components during cytokinesis, and finally physically separate mother and daughter cells to start a new cell cycle apart from each other. To maintain cell size homeostasis and chromosome stability, it is crucial that mechanisms that control growth are connected and coordinated with the cell cycle. Successive periods of high and low TORC1 activity would participate in the adequate cell cycle progression. Here, we review the known molecular mechanisms through which TORC1 regulates the cell cycle in the budding yeast Saccharomyces cerevisiae that have been extensively used as a model organism to understand the role of its mammalian ortholog, mTORC1.
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页数:22
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