| Literature DB >> 32770107 |
Ayan Chanda1, Yoshiho Ikeuchi2,3, Kunal Karve1, Anusi Sarkar1, Amrita Singh Chandhoke1,4, Lili Deng1, Azad Bonni2, Shirin Bonni5.
Abstract
SUMO E3 ligases specify protein substrates for SUMOylation. The SUMO E3 ligases PIAS1 and TIF1γ target the transcriptional regulator SnoN for SUMOylation leading to suppression of epithelial-mesenchymal transition (EMT). Whether and how TIF1γ and PIAS1 might coordinate SnoN SUMOylation and regulation of EMT remained unknown. Here, we reveal that SnoN associates simultaneously with both TIF1γ and PIAS1, leading to a trimeric protein complex. Hence, PIAS1 and TIF1γ collaborate to promote the SUMOylation of SnoN. Importantly, loss of function studies of PIAS1 and TIF1γ suggest that these E3 ligases act in an interdependent manner to suppress EMT of breast cell-derived tissue organoids. Collectively, our findings unveil a novel mechanism by which SUMO E3 ligases coordinate substrate SUMOylation with biological implications.Entities:
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Year: 2020 PMID: 32770107 PMCID: PMC7853041 DOI: 10.1038/s41418-020-0599-8
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828