CRISPR/Cas9 and piggyBac-mediated footprint-free LRRK2-G2019S knock-in reveals neuronal complexity phenotypes and α-Synuclein modulation in dopaminergic neurons; Walter, Jonas ; Jarazo, Javier et alin Stem Cell Research (2017) Detailed reference viewed: 357 (7 UL) Utilization of stem cells to model Parkinson's disease – current state and future challengesHillje, Anna-Lena ; Schwamborn, Jens Christian ![]() in Future Neurology (2016) Detailed reference viewed: 361 (25 UL) The RNA helicase DDX6 regulates cell-fate specification in neural stem cells via miRNAsNicklas, Sarah ; Okawa, Satoshi ; Hillje, Anna-Lena et alin Nucleic Acids Research (2015) Detailed reference viewed: 352 (30 UL) TRIM32 modulates pluripotency entry and exit by directly regulating Oct4 stability; ; Gonzalez Cano, Laura et alin Scientific Reports (2015) Detailed reference viewed: 376 (11 UL) The neural stem cell fate determinant TRIM32 regulates complex behavioral traitsHillje, Anna-Lena ; ; Pavlou, Maria Angeliki et alin Frontiers in Cellular Neuroscience (2015) Detailed reference viewed: 389 (22 UL) Regulatory feedback loop between TP73 and TRIM32.; Hillje, Anna-Lena ; et alin Cell Death and Disease (2013), 4 The p73 transcription factor is one of the members of the p53 family of tumor suppressors with unique biological functions in processes like neurogenesis, embryonic development and differentiation. For ... [more ▼] The p73 transcription factor is one of the members of the p53 family of tumor suppressors with unique biological functions in processes like neurogenesis, embryonic development and differentiation. For this reason, p73 activity is tightly regulated by multiple mechanisms, including transcription and post-translational modifications. Here, we identified a novel regulatory loop between TAp73 and the E3 ubiquitin ligase tripartite motif protein 32 (TRIM32). TRIM32, a new direct p73 transcriptional target in the context of neural progenitor cells, is differentially regulated by p73. Although TAp73 binds to the TRIM32 promoter and activates its expression, TAp73-induced TRIM32 expression is efficiently repressed by DNp73. TRIM32 in turn physically interacts with TAp73 and promotes its ubiquitination and degradation, impairing p73-dependent transcriptional activity. This mutual regulation between p73 and TRIM32 constitutes a novel feedback loop, which might have important implications in central nervous system development as well as relevance in oncogenesis, and thus emerges as a possible therapeutic target. [less ▲] Detailed reference viewed: 392 (11 UL) TRIM32-dependent transcription in adult neural progenitor cells regulates neuronal differentiationHillje, Anna-Lena ; Pavlou, Maria Angeliki ; et alin Cell Death and Disease (2013) Detailed reference viewed: 352 (12 UL) |
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