Mouse models to investigate in situ cell fate decisions induced by p53

Investigating how transcription factors control complex cellular processes requires tools that enable responses to be visualised at the single-cell level and their cell fate to be followed over time. For example, the tumour suppressor p53 (also called TP53 in humans and TRP53 in mice) can initiate diverse cellular responses by transcriptional activation of its target genes: Puma to induce apoptotic cell death and p21 to induce cell cycle arrest/cell senescence. However, it is not known how these processes are regulated and initiated in different cell types. Also, the context-dependent interaction partners and binding loci of p53 remain largely elusive. To be able to examine these questions, we here developed knock-in mice expressing triple-FLAG-tagged p53 to facilitate p53 pull-down and two p53 response reporter mice, knocking tdTomato and GFP into the Puma/Bbc3 and p21 gene loci, respectively. By crossing these reporter mice into a p53-deficient background, we show that the new reporters reliably inform on p53-dependent and p53-independent initiation of both apoptotic or cell cycle arrest/senescence programs, respectively, in vitro and in vivo.

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Publication Details

Journal
The EMBO Journal
Published
2024-08-19
DOI
https://doi.org/10.1038/s44318-024-00189-z
Citations
2
Primary Topic
Cancer-related Molecular Pathways
Type
article
Field-Weighted Citation Impact
0.57

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article

Mouse models to investigate in situ cell fate decisions induced by p53

Gemma L. Kelly, Pedro L. Baldoni, Annabella Thomas, Elizabeth Lieschke et al.
2 citations
The EMBO Journal
Cancer-related Molecular Pathways
0.57
article

Mouse models to investigate in situ cell fate decisions induced by p53

Gemma L. Kelly, Pedro L. Baldoni, Annabella Thomas, Elizabeth Lieschke, Deeksha Kaloni, Savannah Young, Aisling M. Ross, Allan Shuai Huang, Andreas Strasser, Andrew J. Kueh, Edwin D. Hawkins, Gordon K. Smyth, Georgia K. Atkin‐Smith, John E. La Marca, Marco J. Herold, Lin Tai, Lauren Whelan
article en
2 citations

Abstract

Investigating how transcription factors control complex cellular processes requires tools that enable responses to be visualised at the single-cell level and their cell fate to be followed over time. For example, the tumour suppressor p53 (also called TP53 in humans and TRP53 in mice) can initiate diverse cellular responses by transcriptional activation of its target genes: Puma to induce apoptotic cell death and p21 to induce cell cycle arrest/cell senescence. However, it is not known how these processes are regulated and initiated in different cell types. Also, the context-dependent interaction partners and binding loci of p53 remain largely elusive. To be able to examine these questions, we here developed knock-in mice expressing triple-FLAG-tagged p53 to facilitate p53 pull-down and two p53 response reporter mice, knocking tdTomato and GFP into the Puma/Bbc3 and p21 gene loci, respectively. By crossing these reporter mice into a p53-deficient background, we show that the new reporters reliably inform on p53-dependent and p53-independent initiation of both apoptotic or cell cycle arrest/senescence programs, respectively, in vitro and in vivo.

The EMBO JournalVol. 43(19)
The University of Melbourne (AU), Walter and Eliza Hall Institute of Medical Research (AU), La Trobe University (AU), University of Limerick (IE), The Francis Crick Institute (GB), Olivia Newton-John Cancer Wellness & Research Centre (AU)
Victorian Cancer Agency, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 28%
Cancer-related Molecular Pathways
0.57
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