YY1年
脱氮酶
泛素
癌症研究
基因敲除
结直肠癌
转录因子
生物
磷酸化
蛋白酵素
蛋白酶体
细胞生物学
癌症
基因
基因表达
发起人
遗传学
生物化学
酶
作者
Liang Wu,Zili Zhou,Yang Yu,Can Cheng,Shuai Zhou,Yan Yuan,Bofan Yu,Yuwei Zhang,Z. Liu
标识
DOI:10.1038/s41419-024-06526-8
摘要
Abstract Yin Yang 1 (YY1) is a key transcription factor that has been implicated in the development of several malignancies. The stability of YY1 is regulated by the ubiquitin-proteasome system. The role of deubiquitinases (DUBs) and their impact on YY1 remain to be fully elucidated. In this study, we screened for ubiquitin-specific proteases that interact with YY1, and identified OTUD3 as a DUB for YY1. Over-expressed OTUD3 inhibited YY1 degradation, thereby increasing YY1 protein levels, whereas OTUD3 knockdown or knockout promoted YY1 degradation, thereby decreasing the proliferation of colorectal cancer (CRC). Furthermore, PLK1 mediates OTUD3 S326 phosphorylation, which further enhances OTUD3 binding and deubiquitination of YY1. In CRC tissues, elevated the expression level of OTUD3 and YY1 were significantly associated with poor prognostic outcomes. These findings suggest that the OTUD3-YY1 pathway has therapeutic potential in CRC, and OTUD3 plays a critical role in regulating YY1.
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