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CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65
The E3 ubiquitin ligase complex CDC20‐activated anaphase‐promoting complex/Cyclosome (APC/C(CDC20)) plays a critical role in governing mitotic progression by targeting key cell cycle regulators for degradation. Cell division cycle protein 20 homolog (CDC20), the co‐activator of APC/C, is required fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419691/ https://www.ncbi.nlm.nih.gov/pubmed/34382737 http://dx.doi.org/10.15252/embr.202152576 |
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author | Du, Yangge Zhang, Min Liu, Xuejiao Li, Zheng Hu, Menglong Tian, Yueming Lv, Longwei Zhang, Xiao Liu, Yunsong Zhang, Ping Zhou, Yongsheng |
author_facet | Du, Yangge Zhang, Min Liu, Xuejiao Li, Zheng Hu, Menglong Tian, Yueming Lv, Longwei Zhang, Xiao Liu, Yunsong Zhang, Ping Zhou, Yongsheng |
author_sort | Du, Yangge |
collection | PubMed |
description | The E3 ubiquitin ligase complex CDC20‐activated anaphase‐promoting complex/Cyclosome (APC/C(CDC20)) plays a critical role in governing mitotic progression by targeting key cell cycle regulators for degradation. Cell division cycle protein 20 homolog (CDC20), the co‐activator of APC/C, is required for full ubiquitin ligase activity. In addition to its well‐known cell cycle‐related functions, we demonstrate that CDC20 plays an essential role in osteogenic commitment of bone marrow mesenchymal stromal/stem cells (BMSCs). Cdc20 conditional knockout mice exhibit decreased bone formation and impaired bone regeneration after injury. Mechanistically, we discovered a functional interaction between the WD40 domain of CDC20 and the DNA‐binding domain of p65. Moreover, CDC20 promotes the ubiquitination and degradation of p65 in an APC11‐dependent manner. More importantly, knockdown of p65 rescues the bone loss in Cdc20 conditional knockout mice. Our current work reveals a cell cycle‐independent function of CDC20, establishes APC11(CDC20) as a pivotal regulator for bone formation by governing the ubiquitination and degradation of p65, and may pave the way for treatment of bone‐related diseases. |
format | Online Article Text |
id | pubmed-8419691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84196912021-09-13 CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 Du, Yangge Zhang, Min Liu, Xuejiao Li, Zheng Hu, Menglong Tian, Yueming Lv, Longwei Zhang, Xiao Liu, Yunsong Zhang, Ping Zhou, Yongsheng EMBO Rep Articles The E3 ubiquitin ligase complex CDC20‐activated anaphase‐promoting complex/Cyclosome (APC/C(CDC20)) plays a critical role in governing mitotic progression by targeting key cell cycle regulators for degradation. Cell division cycle protein 20 homolog (CDC20), the co‐activator of APC/C, is required for full ubiquitin ligase activity. In addition to its well‐known cell cycle‐related functions, we demonstrate that CDC20 plays an essential role in osteogenic commitment of bone marrow mesenchymal stromal/stem cells (BMSCs). Cdc20 conditional knockout mice exhibit decreased bone formation and impaired bone regeneration after injury. Mechanistically, we discovered a functional interaction between the WD40 domain of CDC20 and the DNA‐binding domain of p65. Moreover, CDC20 promotes the ubiquitination and degradation of p65 in an APC11‐dependent manner. More importantly, knockdown of p65 rescues the bone loss in Cdc20 conditional knockout mice. Our current work reveals a cell cycle‐independent function of CDC20, establishes APC11(CDC20) as a pivotal regulator for bone formation by governing the ubiquitination and degradation of p65, and may pave the way for treatment of bone‐related diseases. John Wiley and Sons Inc. 2021-08-12 2021-09-06 /pmc/articles/PMC8419691/ /pubmed/34382737 http://dx.doi.org/10.15252/embr.202152576 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Du, Yangge Zhang, Min Liu, Xuejiao Li, Zheng Hu, Menglong Tian, Yueming Lv, Longwei Zhang, Xiao Liu, Yunsong Zhang, Ping Zhou, Yongsheng CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 |
title | CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 |
title_full | CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 |
title_fullStr | CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 |
title_full_unstemmed | CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 |
title_short | CDC20 promotes bone formation via APC/C dependent ubiquitination and degradation of p65 |
title_sort | cdc20 promotes bone formation via apc/c dependent ubiquitination and degradation of p65 |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419691/ https://www.ncbi.nlm.nih.gov/pubmed/34382737 http://dx.doi.org/10.15252/embr.202152576 |
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