Zmat3 is a key splicing regulator in the p53 tumor suppression program Journal Article


Authors: Bieging-Rolett, K. T.; Kaiser, A. M.; Morgens, D. W.; Boutelle, A. M.; Seoane, J. A.; Van Nostrand, E. L.; Zhu, C.; Houlihan, S. L.; Mello, S. S.; Yee, B. A.; McClendon, J.; Pierce, S. E.; Winters, I. P.; Wang, M.; Connolly, A. J.; Lowe, S. W.; Curtis, C.; Yeo, G. W.; Winslow, M. M.; Bassik, M. C.; Attardi, L. D.
Article Title: Zmat3 is a key splicing regulator in the p53 tumor suppression program
Abstract: p53 is a critically important but incompletely understood tumor suppressor. Bieging-Rolett et al. identify the p53 target gene Zmat3, encoding an RNA-binding protein, as a key tumor suppressor downstream of p53 in a broad range of cancers and uncover a role for ZMAT3 in regulating alternative RNA splicing. © 2020 Elsevier Inc. Although TP53 is the most commonly mutated gene in human cancers, the p53-dependent transcriptional programs mediating tumor suppression remain incompletely understood. Here, to uncover critical components downstream of p53 in tumor suppression, we perform unbiased RNAi and CRISPR-Cas9-based genetic screens in vivo. These screens converge upon the p53-inducible gene Zmat3, encoding an RNA-binding protein, and we demonstrate that ZMAT3 is an important tumor suppressor downstream of p53 in mouse KrasG12D-driven lung and liver cancers and human carcinomas. Integrative analysis of the ZMAT3 RNA-binding landscape and transcriptomic profiling reveals that ZMAT3 directly modulates exon inclusion in transcripts encoding proteins of diverse functions, including the p53 inhibitors MDM4 and MDM2, splicing regulators, and components of varied cellular processes. Interestingly, these exons are enriched in NMD signals, and, accordingly, ZMAT3 broadly affects target transcript stability. Collectively, these studies reveal ZMAT3 as a novel RNA-splicing and homeostasis regulator and a key component of p53-mediated tumor suppression. © 2020 Elsevier Inc.
Keywords: hepatocellular carcinoma; lung adenocarcinoma; alternative splicing; p53; tumor suppression; mdm4; rnai screen; crispr screen; rbp; zmat3
Journal Title: Molecular Cell
Volume: 80
Issue: 3
ISSN: 1097-2765
Publisher: Cell Press  
Date Published: 2020-11-05
Start Page: 452
End Page: 469.e9
Language: English
DOI: 10.1016/j.molcel.2020.10.022
PUBMED: 33157015
PROVIDER: scopus
PMCID: PMC7654708
DOI/URL:
Notes: Article -- Export Date: 1 December 2020 -- Source: Scopus
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  1. Changyu Zhu
    9 Zhu