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Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol

Cyclins and cyclin-dependent kinases (CDKs) regulate the cell cycle, which is important for cell proliferation and development. Cyclins bind to and activate CDKs, which then drive the cell cycle. The expression of cyclins periodically changes throughout the cell cycle, while that of CDKs remains con...

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Autores principales: Iizumi, Yosuke, Sowa, Yoshihiro, Goi, Wakana, Aono, Yuichi, Watanabe, Motoki, Kurumida, Yoichi, Kameda, Tomoshi, Akaji, Kenichi, Kitagawa, Masatoshi, Sakai, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184650/
https://www.ncbi.nlm.nih.gov/pubmed/35681048
http://dx.doi.org/10.1038/s42003-022-03522-6
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author Iizumi, Yosuke
Sowa, Yoshihiro
Goi, Wakana
Aono, Yuichi
Watanabe, Motoki
Kurumida, Yoichi
Kameda, Tomoshi
Akaji, Kenichi
Kitagawa, Masatoshi
Sakai, Toshiyuki
author_facet Iizumi, Yosuke
Sowa, Yoshihiro
Goi, Wakana
Aono, Yuichi
Watanabe, Motoki
Kurumida, Yoichi
Kameda, Tomoshi
Akaji, Kenichi
Kitagawa, Masatoshi
Sakai, Toshiyuki
author_sort Iizumi, Yosuke
collection PubMed
description Cyclins and cyclin-dependent kinases (CDKs) regulate the cell cycle, which is important for cell proliferation and development. Cyclins bind to and activate CDKs, which then drive the cell cycle. The expression of cyclins periodically changes throughout the cell cycle, while that of CDKs remains constant. To elucidate the mechanisms underlying the constant expression of CDKs, we search for compounds that alter their expression and discover that the natural product fucoxanthinol downregulates CDK2, 4, and 6 expression. We then develop a method to immobilize a compound with a hydroxyl group onto FG beads(®) and identify human ribosomal protein uS7 (also known as ribosomal protein S5) as the major fucoxanthinol-binding protein using the beads and mass spectrometry. The knockdown of uS7 induces G1 cell cycle arrest with the downregulation of CDK6 in colon cancer cells. CDK6, but not CDK2 or CDK4, is degraded by the depletion of uS7, and we furthermore find that uS7 directly binds to CDK6. Fucoxanthinol decreases uS7 at the protein level in colon cancer cells. By identifying the binding proteins of a natural product, the present study reveals that ribosomal protein uS7 may contribute to the constant expression of CDK6 via a direct interaction.
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spelling pubmed-91846502022-06-11 Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol Iizumi, Yosuke Sowa, Yoshihiro Goi, Wakana Aono, Yuichi Watanabe, Motoki Kurumida, Yoichi Kameda, Tomoshi Akaji, Kenichi Kitagawa, Masatoshi Sakai, Toshiyuki Commun Biol Article Cyclins and cyclin-dependent kinases (CDKs) regulate the cell cycle, which is important for cell proliferation and development. Cyclins bind to and activate CDKs, which then drive the cell cycle. The expression of cyclins periodically changes throughout the cell cycle, while that of CDKs remains constant. To elucidate the mechanisms underlying the constant expression of CDKs, we search for compounds that alter their expression and discover that the natural product fucoxanthinol downregulates CDK2, 4, and 6 expression. We then develop a method to immobilize a compound with a hydroxyl group onto FG beads(®) and identify human ribosomal protein uS7 (also known as ribosomal protein S5) as the major fucoxanthinol-binding protein using the beads and mass spectrometry. The knockdown of uS7 induces G1 cell cycle arrest with the downregulation of CDK6 in colon cancer cells. CDK6, but not CDK2 or CDK4, is degraded by the depletion of uS7, and we furthermore find that uS7 directly binds to CDK6. Fucoxanthinol decreases uS7 at the protein level in colon cancer cells. By identifying the binding proteins of a natural product, the present study reveals that ribosomal protein uS7 may contribute to the constant expression of CDK6 via a direct interaction. Nature Publishing Group UK 2022-06-09 /pmc/articles/PMC9184650/ /pubmed/35681048 http://dx.doi.org/10.1038/s42003-022-03522-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Iizumi, Yosuke
Sowa, Yoshihiro
Goi, Wakana
Aono, Yuichi
Watanabe, Motoki
Kurumida, Yoichi
Kameda, Tomoshi
Akaji, Kenichi
Kitagawa, Masatoshi
Sakai, Toshiyuki
Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol
title Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol
title_full Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol
title_fullStr Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol
title_full_unstemmed Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol
title_short Stabilization of CDK6 by ribosomal protein uS7, a target protein of the natural product fucoxanthinol
title_sort stabilization of cdk6 by ribosomal protein us7, a target protein of the natural product fucoxanthinol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184650/
https://www.ncbi.nlm.nih.gov/pubmed/35681048
http://dx.doi.org/10.1038/s42003-022-03522-6
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