TP53 copy number expansion is associated with the evolution of increased body size and an enhanced DNA damage response in elephants

By Michael Sulak, Lindsey Fong, Katelyn M. Mika, Sravanthi Chigurupati, L. Yon, N. Mongan, Richard D Emes, Vincent J. Lynch. bioRxiv, 2015

262 citations recorded by the source corpus.

A major constraint on the evolution of large body sizes in animals is an increased risk of developing cancer. There is no correlation, however, between body size and cancer risk. This lack of correlation is often referred to as ‘Peto’s Paradox’. Here we show that the elephant genome encodes 20 copies of the tumor suppressor gene TP53 and that the increase in TP53 copy number occurred coincident with the evolution of large body sizes, the evolution of extreme sensitivity to genotoxic stress, and a hyperactive TP53 signaling pathway in the elephant (Proboscidean) lineage. Furthermore we show that several of the TP53 retrogenes (TP53RTGs) are transcribed and likely translated. While TP53RTGs do not appear to directly function as transcription factors, they do contribute to the enhanced sensitivity of elephant cells to DNA damage and the induction of apoptosis by regulating activity of the TP53 signaling pathway. These results suggest that an increase in the copy number of TP53 may have played a direct role in the evolution of very large body sizes and the resolution of Peto’s paradox in Proboscideans.

Subfields: Cancer Research, Molecular Biology, Oncology

View Paper: https://www.semanticscholar.org/paper/4afced59738f18a47040e18dbbaa6b89e60c97d8

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Citations in the corpus

• Gene3D: Extensive prediction of globular domains in proteins (2017, background): “We can see a number of features, such as large-scale gene duplication of P53 in elephants producing a number of paralogs (Figure 2A) (which has relevance to cancer suppression in these large, long-lived mammals (14)).”