4.7 Article

Chemoproteomic profiling of O-GlcNAcylated proteins and identification of O-GlcNAc transferases in rice

期刊

PLANT BIOTECHNOLOGY JOURNAL
卷 21, 期 4, 页码 742-753

出版社

WILEY
DOI: 10.1111/pbi.13991

关键词

rice; O-GlcNAcylation; chemoproteomic; metabolic glycan labelling; HCD-pd-EThcD; plant glycobiology

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This study identified O-GlcNAcylation sites and proteins in rice through a large-scale analysis. The O-GlcNAcylated proteins were found to be involved in multiple biological processes such as transcription, translation, and plant hormone signaling. Additionally, two O-GlcNAc transferases were discovered in rice. This research provides a valuable resource for studying O-GlcNAc biology in rice and the MGL method can facilitate the identification of O-GlcNAcylated proteins in various plants.
O-linked beta-N-acetylglucosaminylation (O-GlcNAcylation) is a ubiquitous post-translation modification occurring in both animals and plants. Thousands of proteins along with their O-GlcNAcylation sites have been identified in various animal systems, yet the O-GlcNAcylated proteomes in plants remain poorly understood. Here, we report a large-scale profiling of protein O-GlcNAcylation in a site-specific manner in rice. We first established the metabolic glycan labelling (MGL) strategy with N-azidoacetylgalactosamine (GalNAz) in rice seedlings, which enabled incorporation of azides as a bioorthogonal handle into O-GlcNAc. By conjugation of the azide-incorporated O-GlcNAc with alkyne-biotin containing a cleavable linker via click chemistry, O-GlcNAcylated proteins were selectively enriched for mass spectrometry (MS) analysis. A total of 1591 unambiguous O-GlcNAcylation sites distributed on 709 O-GlcNAcylated proteins were identified. Additionally, 102 O-GlcNAcylated proteins were identified with their O-GlcNAcylation sites located within serine/threonine-enriched peptides, causing ambiguous site assignment. The identified O-GlcNAcylated proteins are involved in multiple biological processes, such as transcription, translation and plant hormone signalling. Furthermore, we discovered two O-GlcNAc transferases (OsOGTs) in rice. By expressing OsOGTs in Escherichia coli and Nicotiana benthamiana leaves, we confirmed their OGT enzymatic activities and used them to validate the identified rice O-GlcNAcylated proteins. Our dataset provides a valuable resource for studying O-GlcNAc biology in rice, and the MGL method should facilitate the identification of O-GlcNAcylated proteins in various plants.

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