The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth

Cell size is amenable by genetic and environmental factors. The highly conserved nutrient-responsive Target of Rapamycin (TOR) signaling pathway regulates cellular metabolic status and growth in response to numerous inputs. Timing and duration of TOR pathway activity is pivotal for both cell mass bu...

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Main Authors: Suam Gonzalez, Charalampos Rallis
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fcell.2017.00061/full
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author Suam Gonzalez
Charalampos Rallis
author_facet Suam Gonzalez
Charalampos Rallis
author_sort Suam Gonzalez
collection DOAJ
description Cell size is amenable by genetic and environmental factors. The highly conserved nutrient-responsive Target of Rapamycin (TOR) signaling pathway regulates cellular metabolic status and growth in response to numerous inputs. Timing and duration of TOR pathway activity is pivotal for both cell mass built up as well as cell cycle progression and is controlled and fine-tuned by the abundance and quality of nutrients, hormonal signals, growth factors, stress, and oxygen. TOR kinases function within two functionally and structurally discrete multiprotein complexes, TORC1 and TORC2, that are implicated in temporal and spatial control of cell size and growth respectively; however, recent data indicate that such functional distinctions are much more complex. Here, we briefly review roles of the two complexes in cellular growth and cytoarchitecture in various experimental model systems.
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spelling doaj.art-0375fe8745d34dcd9ffba893dffc72c02022-12-22T02:34:42ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2017-06-01510.3389/fcell.2017.00061267512The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and GrowthSuam GonzalezCharalampos RallisCell size is amenable by genetic and environmental factors. The highly conserved nutrient-responsive Target of Rapamycin (TOR) signaling pathway regulates cellular metabolic status and growth in response to numerous inputs. Timing and duration of TOR pathway activity is pivotal for both cell mass built up as well as cell cycle progression and is controlled and fine-tuned by the abundance and quality of nutrients, hormonal signals, growth factors, stress, and oxygen. TOR kinases function within two functionally and structurally discrete multiprotein complexes, TORC1 and TORC2, that are implicated in temporal and spatial control of cell size and growth respectively; however, recent data indicate that such functional distinctions are much more complex. Here, we briefly review roles of the two complexes in cellular growth and cytoarchitecture in various experimental model systems.http://journal.frontiersin.org/article/10.3389/fcell.2017.00061/fullcell sizecell cyclegrowthrapamycinsignalingnutrients
spellingShingle Suam Gonzalez
Charalampos Rallis
The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth
Frontiers in Cell and Developmental Biology
cell size
cell cycle
growth
rapamycin
signaling
nutrients
title The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth
title_full The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth
title_fullStr The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth
title_full_unstemmed The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth
title_short The TOR Signaling Pathway in Spatial and Temporal Control of Cell Size and Growth
title_sort tor signaling pathway in spatial and temporal control of cell size and growth
topic cell size
cell cycle
growth
rapamycin
signaling
nutrients
url http://journal.frontiersin.org/article/10.3389/fcell.2017.00061/full
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