Year: 2008
Type: article
Abstract: Nuclear factor of activated T cells (NFATc4) has been implicated as a critical regulator of the cardiac development and hypertrophy. However, the mechanisms for regulating NFATc4 stability and transactivation remain unclear. We showed that NFATc4 protein was predominantly ubiquitinated through the formation of Lysine 48-linked polyubiquitin chains, and this modification decreased NFATc4 protein levels and its transcriptional activity. Furthermore, activation of GSK3beta markedly enhanced NFATc4 ubiquitination and decreased its transactivation, whereas inhibition of GSK3beta had opposite effects. Importantly, ubiquitination and phosphorylation induced by GSK3beta repressed NFATc4-dependent cardiac-specific gene expression. These results demonstrate that the ubiquitin-proteasome system plays an important role in regulating NFATc4 stability and transactivation.
Source: FEBS Letters
Authors: Yongna Fan, Ping Xie, Tianpeng Zhang, Hua Zhang, Dongfeng Gu, Mingpeng She, Huihua Li
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze
Award: 泛素连接酶E3抑制心肌细胞肥大分子病理学机制
OpenAlex ID: W2080215629
