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  • O-GlcNAcylation Antagonizes Phosphorylation of CDH1 (CDC20 Homologue 1).

O-GlcNAcylation Antagonizes Phosphorylation of CDH1 (CDC20 Homologue 1).

The Journal of biological chemistry (2016-04-16)
Jie Tian, Qizhi Geng, Yuehe Ding, Ji Liao, Meng-Qiu Dong, Xingzhi Xu, Jing Li
摘要

The anaphase promoting complex/cyclosome (APC/C) orchestrates various aspects of the eukaryotic cell cycle. One of its co-activators, Cdh1, is subject to myriad post-translational modifications, such as phosphorylation and ubiquitination. Herein we identify the O-linked N-acetylglucosamine (O-GlcNAc) modification that occurs on Cdh1. Cdh1 is O-GlcNAcylated in cultured cells and mouse brain extracts. Mass spectrometry identifies an O-GlcNAcylated peptide that neighbors a known phosphorylation site. Cell synchronization and mutation studies reveal that O-GlcNAcylation of Cdh1 may antagonize its phosphorylation. Our results thus reveal a pivotal role of O-GlcNAcylation in regulating APC/C activity.

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抗-磷酸化-Ser/Thr-Pro,MPM-2抗体, clone MPM-2, Upstate®, from mouse