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The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins

D-type cyclins (cyclin D1, D2, and D3, together cyclin D) are central drivers of the cell division cycle and well-described proto-oncoproteins. Rapid turnover of cyclin D is critical for its regulation, but the underlying mechanism has remained a matter of debate. Recently, AMBRA1 was identified as...

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Autores principales: Chaikovsky, Andrea C., Sage, Julien, Pagano, Michele, Simoneschi, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742259/
https://www.ncbi.nlm.nih.gov/pubmed/34495753
http://dx.doi.org/10.1089/dna.2021.0659
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author Chaikovsky, Andrea C.
Sage, Julien
Pagano, Michele
Simoneschi, Daniele
author_facet Chaikovsky, Andrea C.
Sage, Julien
Pagano, Michele
Simoneschi, Daniele
author_sort Chaikovsky, Andrea C.
collection PubMed
description D-type cyclins (cyclin D1, D2, and D3, together cyclin D) are central drivers of the cell division cycle and well-described proto-oncoproteins. Rapid turnover of cyclin D is critical for its regulation, but the underlying mechanism has remained a matter of debate. Recently, AMBRA1 was identified as the major regulator of the stability of all three D-type cyclins. AMBRA1 serves as the substrate receptor for one of ∼40 CUL4-RING E3 ubiquitin ligase (CRL4) complexes to mediate the polyubiquitylation and subsequent degradation of cyclin D. Consequently, AMBRA1 regulates cell proliferation to impact tumor growth and the cellular response to cell cycle-targeted cancer therapies. Here we discuss the findings that implicate AMBRA1 as a core member of the cell cycle machinery.
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spelling pubmed-87422592022-01-10 The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins Chaikovsky, Andrea C. Sage, Julien Pagano, Michele Simoneschi, Daniele DNA Cell Biol DNACB Bits D-type cyclins (cyclin D1, D2, and D3, together cyclin D) are central drivers of the cell division cycle and well-described proto-oncoproteins. Rapid turnover of cyclin D is critical for its regulation, but the underlying mechanism has remained a matter of debate. Recently, AMBRA1 was identified as the major regulator of the stability of all three D-type cyclins. AMBRA1 serves as the substrate receptor for one of ∼40 CUL4-RING E3 ubiquitin ligase (CRL4) complexes to mediate the polyubiquitylation and subsequent degradation of cyclin D. Consequently, AMBRA1 regulates cell proliferation to impact tumor growth and the cellular response to cell cycle-targeted cancer therapies. Here we discuss the findings that implicate AMBRA1 as a core member of the cell cycle machinery. Mary Ann Liebert, Inc., publishers 2021-12-01 2021-12-16 /pmc/articles/PMC8742259/ /pubmed/34495753 http://dx.doi.org/10.1089/dna.2021.0659 Text en © Andrea C. Chaikovsky et al. 2021; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by-nc/4.0/This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License [CC-BY-NC] (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle DNACB Bits
Chaikovsky, Andrea C.
Sage, Julien
Pagano, Michele
Simoneschi, Daniele
The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins
title The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins
title_full The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins
title_fullStr The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins
title_full_unstemmed The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins
title_short The Long-Lost Ligase: CRL4(AMBRA1) Regulates the Stability of D-Type Cyclins
title_sort long-lost ligase: crl4(ambra1) regulates the stability of d-type cyclins
topic DNACB Bits
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742259/
https://www.ncbi.nlm.nih.gov/pubmed/34495753
http://dx.doi.org/10.1089/dna.2021.0659
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