OCT4 Impedes Cell Fate Redirection By The Melanocyte Lineage Master Regulator MITF
Danna SheinboimiD, Itay MazaiD, Iris DroriD, Shivang ParikhiD, Vladislav Krupalnik, Rachel E. Bell, Asaf ZviraniD, Yusuke SuitaiD, Ofir HakimiD, Yael Mandel‐GutfreundiD, Mehdi KhalediD, Jacob H. HannaiD, Carmit LevyiD
Abstract
Ectopic expression of lineage master regulators induces transdifferentiation. Whether cell fate transitions can be induced during various developmental stages has never been systemically examined. Here we discovered that amongst different developmental stages, embryonic stem cells (ESCs) were resistant to cell fate conversion induced by the melanocyte lineage master regulator MITF. We generated a transgenic system and found that in ESCs, the pluripotency master regulator, OCT4, counteracts pro-differentiation induced by MITF by physical interference with MITF transcriptional activity. We further found that ESCs must be released from OCT4-maintained pluripotency prior to ectopically induced differentiation. Moreover, OCT4 induction in various differentiated cells repressed their lineage identity in vivo. Alongside, chromatin architecture combined with ChIP-seq analysis suggested that OCT4 competes with various lineage master regulators for binding promoters and enhancers. Our analysis reveals pluripotency and transdifferentiation regulatory principles and could open new opportunities in the field of regenerative medicine.
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