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Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear

Mechanistic target of rapamycin complex 1 (mTORC1) is a well-known regulator of cell growth and proliferation in response to environmental stimuli and stressors. To date, the majority of mTORC1 studies have focused on its function as a cytoplasmic effector of translation regulation. However, recent...

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Detalles Bibliográficos
Autores principales: Workman, Jason J, Chen, Hongfeng, Laribee, R Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979908/
https://www.ncbi.nlm.nih.gov/pubmed/24526113
http://dx.doi.org/10.4161/cc.28112
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author Workman, Jason J
Chen, Hongfeng
Laribee, R Nicholas
author_facet Workman, Jason J
Chen, Hongfeng
Laribee, R Nicholas
author_sort Workman, Jason J
collection PubMed
description Mechanistic target of rapamycin complex 1 (mTORC1) is a well-known regulator of cell growth and proliferation in response to environmental stimuli and stressors. To date, the majority of mTORC1 studies have focused on its function as a cytoplasmic effector of translation regulation. However, recent studies have identified additional, nuclear-specific roles for mTORC1 signaling related to transcription of the ribosomal DNA (rDNA) and ribosomal protein (RP) genes, mitotic cell cycle control, and the regulation of epigenetic processes. As this area of study is still in its infancy, the purpose of this review to highlight these significant findings and discuss the relevance of nuclear mTORC1 signaling dysregulation as it pertains to health and disease.
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spelling pubmed-39799082014-04-10 Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear Workman, Jason J Chen, Hongfeng Laribee, R Nicholas Cell Cycle Review Mechanistic target of rapamycin complex 1 (mTORC1) is a well-known regulator of cell growth and proliferation in response to environmental stimuli and stressors. To date, the majority of mTORC1 studies have focused on its function as a cytoplasmic effector of translation regulation. However, recent studies have identified additional, nuclear-specific roles for mTORC1 signaling related to transcription of the ribosomal DNA (rDNA) and ribosomal protein (RP) genes, mitotic cell cycle control, and the regulation of epigenetic processes. As this area of study is still in its infancy, the purpose of this review to highlight these significant findings and discuss the relevance of nuclear mTORC1 signaling dysregulation as it pertains to health and disease. Landes Bioscience 2014-03-01 2014-02-07 /pmc/articles/PMC3979908/ /pubmed/24526113 http://dx.doi.org/10.4161/cc.28112 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Workman, Jason J
Chen, Hongfeng
Laribee, R Nicholas
Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear
title Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear
title_full Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear
title_fullStr Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear
title_full_unstemmed Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear
title_short Environmental signaling through the mechanistic target of rapamycin complex 1: mTORC1 goes nuclear
title_sort environmental signaling through the mechanistic target of rapamycin complex 1: mtorc1 goes nuclear
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979908/
https://www.ncbi.nlm.nih.gov/pubmed/24526113
http://dx.doi.org/10.4161/cc.28112
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