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Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase

Most Cyclin-dependent kinases (Cdks) are redundant for normal cell division. Here we tested whether these redundancies are maintained during cell cycle recovery after a DNA damage-induced arrest in G1. Using non-transformed RPE-1 cells, we find that while Cdk4 and Cdk6 act redundantly during normal...

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Autores principales: Shaltiel, Indra A., Llopis, Alba, Aprelia, Melinda, Klompmaker, Rob, Menegakis, Apostolos, Krenning, Lenno, Medema, René H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999910/
https://www.ncbi.nlm.nih.gov/pubmed/33806417
http://dx.doi.org/10.3390/cells10030550
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author Shaltiel, Indra A.
Llopis, Alba
Aprelia, Melinda
Klompmaker, Rob
Menegakis, Apostolos
Krenning, Lenno
Medema, René H.
author_facet Shaltiel, Indra A.
Llopis, Alba
Aprelia, Melinda
Klompmaker, Rob
Menegakis, Apostolos
Krenning, Lenno
Medema, René H.
author_sort Shaltiel, Indra A.
collection PubMed
description Most Cyclin-dependent kinases (Cdks) are redundant for normal cell division. Here we tested whether these redundancies are maintained during cell cycle recovery after a DNA damage-induced arrest in G1. Using non-transformed RPE-1 cells, we find that while Cdk4 and Cdk6 act redundantly during normal S-phase entry, they both become essential for S-phase entry after DNA damage in G1. We show that this is due to a greater overall dependency for Cdk4/6 activity, rather than to independent functions of either kinase. In addition, we show that inactivation of pocket proteins is sufficient to overcome the inhibitory effects of complete Cdk4/6 inhibition in otherwise unperturbed cells, but that this cannot revert the effects of Cdk4/6 inhibition in DNA damaged cultures. Indeed, we could confirm that, in addition to inactivation of pocket proteins, Cdh1-dependent anaphase-promoting complex/cyclosome (APC/C(Cdh1)) activity needs to be inhibited to promote S-phase entry in damaged cultures. Collectively, our data indicate that DNA damage in G1 creates a unique situation where high levels of Cdk4/6 activity are required to inactivate pocket proteins and APC/C(Cdh1) to promote the transition from G1 to S phase.
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spelling pubmed-79999102021-03-28 Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase Shaltiel, Indra A. Llopis, Alba Aprelia, Melinda Klompmaker, Rob Menegakis, Apostolos Krenning, Lenno Medema, René H. Cells Article Most Cyclin-dependent kinases (Cdks) are redundant for normal cell division. Here we tested whether these redundancies are maintained during cell cycle recovery after a DNA damage-induced arrest in G1. Using non-transformed RPE-1 cells, we find that while Cdk4 and Cdk6 act redundantly during normal S-phase entry, they both become essential for S-phase entry after DNA damage in G1. We show that this is due to a greater overall dependency for Cdk4/6 activity, rather than to independent functions of either kinase. In addition, we show that inactivation of pocket proteins is sufficient to overcome the inhibitory effects of complete Cdk4/6 inhibition in otherwise unperturbed cells, but that this cannot revert the effects of Cdk4/6 inhibition in DNA damaged cultures. Indeed, we could confirm that, in addition to inactivation of pocket proteins, Cdh1-dependent anaphase-promoting complex/cyclosome (APC/C(Cdh1)) activity needs to be inhibited to promote S-phase entry in damaged cultures. Collectively, our data indicate that DNA damage in G1 creates a unique situation where high levels of Cdk4/6 activity are required to inactivate pocket proteins and APC/C(Cdh1) to promote the transition from G1 to S phase. MDPI 2021-03-04 /pmc/articles/PMC7999910/ /pubmed/33806417 http://dx.doi.org/10.3390/cells10030550 Text en © 2021 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 (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Shaltiel, Indra A.
Llopis, Alba
Aprelia, Melinda
Klompmaker, Rob
Menegakis, Apostolos
Krenning, Lenno
Medema, René H.
Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase
title Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase
title_full Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase
title_fullStr Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase
title_full_unstemmed Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase
title_short Combined Inactivation of Pocket Proteins and APC/C(Cdh1) by Cdk4/6 Controls Recovery from DNA Damage in G1 Phase
title_sort combined inactivation of pocket proteins and apc/c(cdh1) by cdk4/6 controls recovery from dna damage in g1 phase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999910/
https://www.ncbi.nlm.nih.gov/pubmed/33806417
http://dx.doi.org/10.3390/cells10030550
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