HBO1 catalyzes lysine benzoylation in mammalian cells

  • Doudou Tan
  • , Wei Wei
  • , Zhen Han
  • , Xuelian Ren
  • , Cong Yan
  • , Shankang Qi
  • , Xiaohan Song
  • , Y. George Zheng
  • , Jiemin Wong
  • , He Huang*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

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.

Original languageEnglish
Article number105443
JournaliScience
Volume25
Issue number11
DOIs
StatePublished - 18 Nov 2022

Keywords

  • Biological sciences
  • Cell biology
  • Molecular biology

Fingerprint

Dive into the research topics of 'HBO1 catalyzes lysine benzoylation in mammalian cells'. Together they form a unique fingerprint.

Cite this