Back

The transcription factor Zic4 acts as a transdifferentiation switch

Vogg, M. C.; Ferenc, J.; Buzgariu, W. C.; Perruchoud, C.; Papasaikas, P.; Sanchez, P. G. L.; Nuninger, C.; Delucinge-Vivier, C.; Rampon, C.; Beccari, L.; Vriz, S.; Vincent, S.; Galliot, B.; Tsiairis, C.

2021-12-23 developmental biology
10.1101/2021.12.22.473838 bioRxiv
Show abstract

The molecular mechanisms that maintain cell identities and prevent transdifferentiation remain mysterious. Interestingly, both dedifferentiation and transdifferentiation are transiently reshuffled during regeneration. Therefore, organisms that regenerate readily offer a fruitful paradigm to investigate the regulation of cell fate stability. Here, we used Hydra as a model system and show that Zic4 silencing is sufficient to induce transdifferentiation of tentacle into foot cells. We identified a Wnt-controlled Gene Regulatory Network that controls a transcriptional switch of cell identity. Furthermore, we show that this switch also controls the re-entry into the cell cycle. Our data indicate that maintenance of cell fate by a Wnt-controlled GRN is a key mechanism during both homeostasis and regeneration. One-Sentence SummaryA Wnt-controlled GRN controls fate maintenance in Hydra.

Matching journals

The top 1 journal accounts for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.