Mammalian embryo comparison identifies novel pluripotency genes associated with the naïve or primed state

During early mammalian development, transient pools of pluripotent cells emerge that can be immortalised upon stem cell derivation. The pluripotent state, 'naïve' or 'primed', depends on the embryonic stage and derivation conditions used. Here we analyse the temporal gene express...

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Published inBiology open Vol. 7; no. 8
Main Authors Bernardo, Andreia S, Jouneau, Alice, Marks, Hendrik, Kensche, Philip, Kobolak, Julianna, Freude, Kristine, Hall, Vanessa, Feher, Anita, Polgar, Zsuzsanna, Sartori, Chiara, Bock, Istvan, Louet, Claire, Faial, Tiago, Kerstens, Hindrik H D, Bouissou, Camille, Parsonage, Gregory, Mashayekhi, Kaveh, Smith, James C, Lazzari, Giovanna, Hyttel, Poul, Stunnenberg, Hendrik G, Huynen, Martijn, Pedersen, Roger A, Dinnyes, Andras
Format Journal Article
LanguageEnglish
Published England The Company of Biologists Ltd 2018
Royal Society
The Company of Biologists
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Summary:During early mammalian development, transient pools of pluripotent cells emerge that can be immortalised upon stem cell derivation. The pluripotent state, 'naïve' or 'primed', depends on the embryonic stage and derivation conditions used. Here we analyse the temporal gene expression patterns of mouse, cattle and porcine embryos at stages that harbour different types of pluripotent cells. We document conserved and divergent traits in gene expression, and identify predictor genes shared across the species that are associated with pluripotent states and Amongst these are the pluripotency-linked genes and The novel genes discovered include naïve- ( and ) and primed-associated ( and ) genes as well as naïve to primed transition genes ( and ). Both and play a role in pluripotency since their knockdown results in differentiation and downregulation of key pluripotency genes. Our interspecies comparison revealed new insights of pluripotency, pluripotent stem cell identity and a new molecular criterion for distinguishing between pluripotent states in various species, including human.
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PMCID: PMC6124576
Joint second authors
Joint first authors
ISSN:2046-6390
2046-6390
DOI:10.1242/bio.033282