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PMID: 27339899 已发表 · ppublish 英语

NEDD4L Protein Catalyzes Ubiquitination of PIK3CA Protein and Regulates PI3K-AKT Signaling.

The Journal of biological chemistry ·第 291 卷 ·第 33 期 ·0000-00-00

Wang Zixi, Dang Tingting, Liu Tingting, Chen She, Li Lin, Huang Song, Fang Min

摘要

Oncogenic PIK3CA (p110α), the catalytic subunit of class IA PI3K, plays a major role in PI3K-related cancer progression. The mechanisms underlying the dynamic regulation of PIK3CA protein levels remain unknown. Here we demonstrated that PIK3CA is regulated by polyubiquitination. We identified NEDD4L as the E3 ligase that catalyzes PIK3CA polyubiquitination, leading to its proteasome-dependent degradation. NEDD4L ubiquitinates both the free and regulatory subunit-bound PIK3CA but does not ubiquitinate the regulatory subunit of PI3K. Overexpression of NEDD4L accelerates the turnover rate of PIK3CA, whereas suppression of NEDD4L results in not only the accumulation of PIK3CA but also a paradoxical decrease of AKT activation. Thus, we propose that NEDD4L negatively regulates PIK3CA protein levels via ubiquitination and is required for the maintenance of PI3K-AKT signaling pathway.

关键词
Akt PKB E3 ubiquitin ligase NEDD4L PIK3CA phosphatidylinositide 3-kinase (PI 3-kinase) proteasome protein degradation ubiquitylation (ubiquitination)
文献信息
期刊
The Journal of biological chemistry
期刊简称
J Biol Chem
发表日期
0000-00-00
收录日期
2016-08-13
更新日期
2016-09-13
语言
英语
国家/地区
United States
NLM ID
2985121R
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