E2F8 is essential for polyploidization in mammalian cells.

S.K. Pandit, B. Westendorp, S. Nantasanti, E. van Liere, P.C. Tooten, P.W. Cornelissen, M.J. Toussaint, W.H. Lamers, A. de Bruin

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Abstract

Polyploidization is observed in all mammalian species and is a characteristic feature of hepatocytes, but its molecular mechanism and biological significance are unknown. Hepatocyte polyploidization in rodents occurs through incomplete cytokinesis, starts after weaning and increases with age. Here, we show in mice that atypical E2F8 is induced after weaning and required for hepatocyte binucleation and polyploidization. A deficiency in E2f8 led to an increase in the expression level of E2F target genes promoting cytokinesis and thereby preventing polyploidization. In contrast, loss of E2f1 enhanced polyploidization and suppressed the polyploidization defect of hepatocytes deficient for atypical E2Fs. In addition, E2F8 and E2F1 were found on the same subset of target promoters. Contrary to the long-standing hypothesis that polyploidization indicates terminal differentiation and senescence, we show that prevention of polyploidization through inactivation of atypical E2Fs has, surprisingly, no impact on liver differentiation, zonation, metabolism and regeneration. Together, these results identify E2F8 as a repressor and E2F1 as an activator of a transcriptional network controlling polyploidization in mammalian cells.
Original languageEnglish
Pages (from-to)1181-1191
JournalNature Cell Biology
Volume14
Issue number11
DOIs
Publication statusPublished - 1 Jan 2012

Cite this

Pandit, S. K., Westendorp, B., Nantasanti, S., van Liere, E., Tooten, P. C., Cornelissen, P. W., Toussaint, M. J., Lamers, W. H., & de Bruin, A. (2012). E2F8 is essential for polyploidization in mammalian cells. Nature Cell Biology, 14(11), 1181-1191. https://doi.org/10.1038/ncb2585