Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014;13(5):714-25.
doi: 10.4161/cc.28112. Epub 2014 Feb 7.

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

Affiliations
Review

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

Jason J Workman et al. Cell Cycle. 2014.

Abstract

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.

Keywords: acetylation; cancer; epigenetics; histones; target of rapamycin; transcription.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Laplante M, Sabatini DM. mTOR signaling in growth control and disease. Cell. 2012;149:274–93. doi: 10.1016/j.cell.2012.03.017. - DOI - PMC - PubMed
    1. Loewith R, Hall MN. Target of rapamycin (TOR) in nutrient signaling and growth control. Genetics. 2011;189:1177–201. doi: 10.1534/genetics.111.133363. - DOI - PMC - PubMed
    1. Vézina C, Kudelski A, Sehgal SN. Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the producing streptomycete and isolation of the active principle. J Antibiot (Tokyo) 1975;28:721–6. doi: 10.7164/antibiotics.28.721. - DOI - PubMed
    1. Metcalfe SM, Richards FM. Cyclosporine, FK506, and rapamycin. Some effects on early activation events in serum-free, mitogen-stimulated mouse spleen cells. Transplantation. 1990;49:798–802. doi: 10.1097/00007890-199004000-00028. - DOI - PubMed
    1. Barbet NC, Schneider U, Helliwell SB, Stansfield I, Tuite MF, Hall MN. TOR controls translation initiation and early G1 progression in yeast. Mol Biol Cell. 1996;7:25–42. doi: 10.1091/mbc.7.1.25. - DOI - PMC - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources