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MDM4 exon skipping upon dysfunctional ribosome assembly. | LitMetric

MDM4 exon skipping upon dysfunctional ribosome assembly.

Trends Cell Biol

Department of Molecular Oncology, Göttingen Center of Molecular Biosciences (GZMB), University Medical Center Göttingen, Justus-von-Liebig-Weg 11, 37077 Göttingen, Germany; Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. Electronic address:

Published: November 2024

Recent studies revealed how nucleolar stress enhances MDM4 exon skipping and activates p53 via the ribosomal protein L22 (RPL22; eL22). Tumor-associated L22 mutations lead to full-length MDM4 synthesis, overcoming tumor suppression by p53. This forum article explores how MDM4 splicing patterns integrate stress signaling to take p53-dependent cell fate decisions.

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Source
http://dx.doi.org/10.1016/j.tcb.2024.10.006DOI Listing

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