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HBO1 catalyzes lysine benzoylation in mammalian cells

Lysine benzoylation (Kbz) is a newly discovered protein post-translational modification (PTM). This PTM can be stimulated by benzoate and contributes to gene expression. However, its regulatory enzymes and substrate proteins remain largely unknown, hindering further functional studies. Here we ident...

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Detalles Bibliográficos
Autores principales: Tan, Doudou, Wei, Wei, Han, Zhen, Ren, Xuelian, Yan, Cong, Qi, Shankang, Song, Xiaohan, Zheng, Y. George, Wong, Jiemin, Huang, He
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647509/
https://www.ncbi.nlm.nih.gov/pubmed/36388951
http://dx.doi.org/10.1016/j.isci.2022.105443
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author Tan, Doudou
Wei, Wei
Han, Zhen
Ren, Xuelian
Yan, Cong
Qi, Shankang
Song, Xiaohan
Zheng, Y. George
Wong, Jiemin
Huang, He
author_facet Tan, Doudou
Wei, Wei
Han, Zhen
Ren, Xuelian
Yan, Cong
Qi, Shankang
Song, Xiaohan
Zheng, Y. George
Wong, Jiemin
Huang, He
author_sort Tan, Doudou
collection PubMed
description Lysine benzoylation (Kbz) is a newly discovered protein post-translational modification (PTM). This PTM can be stimulated by benzoate and contributes to gene expression. However, its regulatory enzymes and substrate proteins remain largely unknown, hindering further functional studies. Here we identified and validated the lysine acetyltransferase (KAT) HBO1 as a “writer” of Kbz in mammalian cells. In addition, we report the benzoylome in mammalian cells, identifying 1747 Kbz sites; among them at least 77 are the HBO1-targeted Kbz substrates. Bioinformatics analysis showed that HBO1-targeted Kbz sites were involved in multiple processes, including chromatin remodeling, transcription regulation, immune regulation, and tumor growth. Our results thus identify the regulatory elements of the Kbz pathway and reveal the non-canonical enzymatic activity and functions of HBO1 in cellular physiology.
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spelling pubmed-96475092022-11-15 HBO1 catalyzes lysine benzoylation in mammalian cells Tan, Doudou Wei, Wei Han, Zhen Ren, Xuelian Yan, Cong Qi, Shankang Song, Xiaohan Zheng, Y. George Wong, Jiemin Huang, He iScience Article Lysine benzoylation (Kbz) is a newly discovered protein post-translational modification (PTM). This PTM can be stimulated by benzoate and contributes to gene expression. However, its regulatory enzymes and substrate proteins remain largely unknown, hindering further functional studies. Here we identified and validated the lysine acetyltransferase (KAT) HBO1 as a “writer” of Kbz in mammalian cells. In addition, we report the benzoylome in mammalian cells, identifying 1747 Kbz sites; among them at least 77 are the HBO1-targeted Kbz substrates. Bioinformatics analysis showed that HBO1-targeted Kbz sites were involved in multiple processes, including chromatin remodeling, transcription regulation, immune regulation, and tumor growth. Our results thus identify the regulatory elements of the Kbz pathway and reveal the non-canonical enzymatic activity and functions of HBO1 in cellular physiology. Elsevier 2022-10-26 /pmc/articles/PMC9647509/ /pubmed/36388951 http://dx.doi.org/10.1016/j.isci.2022.105443 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tan, Doudou
Wei, Wei
Han, Zhen
Ren, Xuelian
Yan, Cong
Qi, Shankang
Song, Xiaohan
Zheng, Y. George
Wong, Jiemin
Huang, He
HBO1 catalyzes lysine benzoylation in mammalian cells
title HBO1 catalyzes lysine benzoylation in mammalian cells
title_full HBO1 catalyzes lysine benzoylation in mammalian cells
title_fullStr HBO1 catalyzes lysine benzoylation in mammalian cells
title_full_unstemmed HBO1 catalyzes lysine benzoylation in mammalian cells
title_short HBO1 catalyzes lysine benzoylation in mammalian cells
title_sort hbo1 catalyzes lysine benzoylation in mammalian cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647509/
https://www.ncbi.nlm.nih.gov/pubmed/36388951
http://dx.doi.org/10.1016/j.isci.2022.105443
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