Nature CommunicationsDevelopmental BiologyPeer-reviewed journal article
Evolutionary Origin of Vertebrate OCT4/POU5 Functions in Supporting Pluripotency
Woranop SukparangsiiD, Elena Morganti, Molly LowndesiD, Hélène MayeuriD, Melanie Bianca WeisseriD, Fella Hammachi, Hanna Peradziryi, Fabian V RoskeiD, Jurriaan HölzenspiesiD, Alessandra Livigni, Benoît G. GodardiD, Fumiaki SugaharaiD, Shigeru KurataniiD, Guillermo MontoyaiD, Stephen FrankenbergiD, Sylvie MazaniD, Joshua M. BrickmaniD
Abstract
The support of pluripotent cells over time is an essential feature of development. In eutherian embryos, pluripotency is maintained from naive states in peri-implantation to primed pluripotency at gastrulation. To understand how these states emerged, we reconstruct the evolutionary trajectory of the Pou5 gene family, which contains the central pluripotency factor OCT4. By coupling evolutionary sequence analysis with functional studies in mouse Embryonic Stem Cells (ESCs), we found that the ability of POU5 proteins to support pluripotency originated in the gnathostome lineage, prior to the generation of two paralogues, Pou5f1 and Pou5f3 via gene duplication. In osteichthyans, retaining both genes, the paralogues differ in their support of naive and primed pluripotency. This specialization of these duplicates enables the diversification of function in self-renewal and differentiation. By integrating sequence evolution, ESC phenotypes, developmental contexts and structural modelling, we pinpoint OCT4 regions sufficient for naive pluripotency and describe their adaptation over evolutionary time.
- organism: mouse
- assay: bulk RNA-seq
- research focus: gene regulatory network inference
- approach: statistical model
- approach: experimental assay
- Citations
- 18
- FWCI
- 1.39
- Field percentile
- top 19%
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