| Literature DB >> 29061731 |
Lisheng Li1,2, Hong Yang3, Yan He3, Ting Li3, Jinan Feng3, Wanze Chen4, Lu Ao5,2, Xuying Shi3, Yingying Lin6,2, Haoyun Liu3, Enrun Zheng3, Qiaofa Lin3, Jingjing Bu3, Yanhua Zeng3, Min Zheng3,2, Yan Xu3, Zhijun Liao3, Jiacheng Lin7,2, Dexin Lin1.
Abstract
The c-Jun gene encodes a transcription factor that has been implicated in many physiological and pathological processes. c-Jun is a highly unstable protein that is degraded through a ubiquitination/proteasome-dependent mechanism. However, the deubiquitinating enzyme (DUB) that regulates the stability of the c-Jun protein requires further investigation. Here, by screening a DUB expression library, we identified ubiquitin-specific protease 6 (USP6) and showed that it regulates the stability of the c-Jun protein in a manner depending on its enzyme activity. USP6 interacts with c-Jun and antagonizes its ubiquitination. USP6 overexpression upregulates the activity of the downstream signaling pathway mediated by c-Jun/AP-1 and promotes cell invasion. Moreover, many aberrant genes that are upregulated in USP6 translocated nodular fasciitis are great potential targets regulated by c-Jun. Based on our data, USP6 is an enzyme that deubiquitinates c-Jun and regulates its downstream cellular functions.Entities:
Keywords: USP6; c-Jun; deubiquitinating enzyme; deubiquitination; nodular fasciitis
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Year: 2017 PMID: 29061731 PMCID: PMC5748463 DOI: 10.1128/MCB.00320-17
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272