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Conservation of DNA-binding specificity and oligomerisation properties within the p53 family
Abstract
Background: Transcription factors activate their target genes by binding to specific response elements. Many transcription factor families evolved from a common ancestor by gene duplication and subsequent divergent evolution. Members of the p53 family, which play key roles in cell-cycle control and development, share conserved DNA binding and oligomerisation domains but exhibit distinct functions. In this study, the molecular basis of the functional divergence of related transcription factors was investigated. Results: We characterised the DNA-binding specificity and oligomerisation properties of human p53, p63 and p73, as well as p53 from other organisms using novel biophysical approaches. All p53 family members bound DNA cooperatively as tetramers with high affinity. Despite structural differences in the oligomerisation domain, the dissociation constants of the tetramers was in the low nanomolar range for all family members, indicating that the strength of tetramerisation was evolutionarily conserved. However, small differences in the oligomerisation properties were observed, which may play a regulatory role. Intriguingly, the DNA-binding specificity of p53 family members was highly conserved even for evolutionarily distant species. Additionally, DNA recognition was only weakly affected by CpG methylation. Prediction of p53/p63/p73 binding sites in the genome showed almost complete overlap between the different homologs. Conclusion: Diversity of biological function of p53 family members is not reflected in differences in sequence-specific DNA binding. Hence, additional specificity factors must exist, which allowed the acquisition of novel functions during evolution while preserving original roles.
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“The NMR experiments on full-length p53 were carried out with protein concentrations of at least 30 μM, far above the Kd for p53 tetramerization (50 nM).50,62”
From Mapping Interactions of the Intrinsically Disordered C-Terminal Regions of Tetrameric p53 by Segmental Isotope Labeling and NMR (2022) · cites this paper as [62]
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BackgroundInfluentialDefinition of a consensus binding site for p53
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“p53 is at the centre of a tumour suppressor network [4,5], and, as such, is essential for the prevention of cancer [6,7].”
BackgroundA Global Map of p53 Transcription-Factor Binding Sites in the Human Genome
Wei, C.-L., Wu, Q., Vega, V. B., Chiu, K. P., Ng, P., Zhang, T., Shahab, A., Yong, H. C., Fu, Y., Weng, Z., et al. (2006) · Cell · doi:10.1016/j.cell.2005.10.043 · Cited by 1,141
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Core domain interactions in full-length p53 in solution
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Metadata
- Authors
- Brandt, T., Petrovich, M., Joerger, A. C., & Veprintsev, D. B.
- Venue
- BMC Genomics
- Published
- 2009-12
- Volume
- 10
- Issue
- 1
- ISSN
- 1471-2164
- Cited by
- 73
- References
- 8
- Language
- en
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