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Regulation of Life & Death by REGγ

REGγ, a proteasome activator belonging to the 11S (otherwise known as REG, PA28, or PSME) proteasome activator family, is widely present in many eukaryotes. By binding to the 20S catalytic core particle, REGγ acts as a molecular sieve to selectively target proteins for degradation in an ATP- and ubi...

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Detalles Bibliográficos
Autores principales: Funderburk, Keaton E., Kang, Jungseog, Li, Henry J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330691/
https://www.ncbi.nlm.nih.gov/pubmed/35892577
http://dx.doi.org/10.3390/cells11152281
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author Funderburk, Keaton E.
Kang, Jungseog
Li, Henry J.
author_facet Funderburk, Keaton E.
Kang, Jungseog
Li, Henry J.
author_sort Funderburk, Keaton E.
collection PubMed
description REGγ, a proteasome activator belonging to the 11S (otherwise known as REG, PA28, or PSME) proteasome activator family, is widely present in many eukaryotes. By binding to the 20S catalytic core particle, REGγ acts as a molecular sieve to selectively target proteins for degradation in an ATP- and ubiquitin-independent manner. This non-canonical proteasome pathway directly regulates seemingly unrelated cellular processes including cell growth and proliferation, apoptosis, DNA damage response, immune response, and metabolism. By affecting different pathways, REGγ plays a vital role in the regulation of cellular life and death through the maintenance of protein homeostasis. As a promoter of cellular growth and a key regulator of several tumor suppressors, many recent studies have linked REGγ overexpression with tumor formation and suggested the REGγ-proteasome as a potential target of new cancer-drug development. This review will present an overview of the major functions of REGγ as it relates to the regulation of cellular life and death, along with new mechanistic insights into the regulation of REGγ.
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spelling pubmed-93306912022-07-29 Regulation of Life & Death by REGγ Funderburk, Keaton E. Kang, Jungseog Li, Henry J. Cells Review REGγ, a proteasome activator belonging to the 11S (otherwise known as REG, PA28, or PSME) proteasome activator family, is widely present in many eukaryotes. By binding to the 20S catalytic core particle, REGγ acts as a molecular sieve to selectively target proteins for degradation in an ATP- and ubiquitin-independent manner. This non-canonical proteasome pathway directly regulates seemingly unrelated cellular processes including cell growth and proliferation, apoptosis, DNA damage response, immune response, and metabolism. By affecting different pathways, REGγ plays a vital role in the regulation of cellular life and death through the maintenance of protein homeostasis. As a promoter of cellular growth and a key regulator of several tumor suppressors, many recent studies have linked REGγ overexpression with tumor formation and suggested the REGγ-proteasome as a potential target of new cancer-drug development. This review will present an overview of the major functions of REGγ as it relates to the regulation of cellular life and death, along with new mechanistic insights into the regulation of REGγ. MDPI 2022-07-23 /pmc/articles/PMC9330691/ /pubmed/35892577 http://dx.doi.org/10.3390/cells11152281 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Funderburk, Keaton E.
Kang, Jungseog
Li, Henry J.
Regulation of Life & Death by REGγ
title Regulation of Life & Death by REGγ
title_full Regulation of Life & Death by REGγ
title_fullStr Regulation of Life & Death by REGγ
title_full_unstemmed Regulation of Life & Death by REGγ
title_short Regulation of Life & Death by REGγ
title_sort regulation of life & death by regγ
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330691/
https://www.ncbi.nlm.nih.gov/pubmed/35892577
http://dx.doi.org/10.3390/cells11152281
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