Metabolic labeling based methylome profiling enables functional dissection of histidine methylation in C3H1 zinc fingers

Protein methylation is a functionally important post-translational modification that occurs on diverse amino acid residues. The current proteomics approaches are inefficient to discover the methylation on residues other than Arg and Lys, which hinders the deep understanding of the functional role of...

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Veröffentlicht in:Nature communications 2024-08, Vol.15 (1), p.7459-14, Article 7459
Hauptverfasser: Wang, Keyun, Zhang, Li, Zhang, Sirui, Liu, Ye, Mao, Jiawei, Liu, Zhen, Xu, Lin, Li, Kejia, Wang, Jianshu, Ma, Yanni, Wang, Jiayi, Li, Haitao, Wang, Zefeng, Li, Guohui, Cheng, Hong, Ye, Mingliang
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Sprache:eng
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Zusammenfassung:Protein methylation is a functionally important post-translational modification that occurs on diverse amino acid residues. The current proteomics approaches are inefficient to discover the methylation on residues other than Arg and Lys, which hinders the deep understanding of the functional role of rare protein methylation. Herein, we present a methyl-specific metabolic labeling approach for global methylome mapping, which enable the acquisition of methylome dataset covering diverse methylation types. Interestingly, of the identified methylation events, His methylation is found to be preferably occurred in C3H1 zinc fingers (ZFs). These His methylation events are determined to be Nπ specific and catalyzed by CARNMT1. The His methylation is found to stabilize the structure of ZFs. U2AF1 is used as a proof-of-concept to highlight the functional importance of His methylation in ZFs in RNA binding and RNA metabolism. The results of this study enable novel understanding of how protein methylation regulates cellular processes. Here the authors developed a methyl-specific metabolic labeling approach for global analysis covering diverse methylation types. His methylation is found in C3H1 zinc fingers. U2AF1 is used to highlight the role of His methylation in ZFs in RNA metabolism.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-51979-2