Indirect Mechanisms of Transcription Factor-Mediated Gene Regulation during Cell Fate Changes

Adv Genet (Hoboken). 2022 Nov 9;3(4):2200015. doi: 10.1002/ggn2.202200015. eCollection 2022 Dec.

Abstract

Transcription factors (TFs) are the master regulators of cellular identity, capable of driving cell fate transitions including differentiations, reprogramming, and transdifferentiations. Pioneer TFs recognize partial motifs exposed on nucleosomal DNA, allowing for TF-mediated activation of repressed chromatin. Moreover, there is evidence suggesting that certain TFs can repress actively expressed genes either directly through interactions with accessible regulatory elements or indirectly through mechanisms that impact the expression, activity, or localization of other regulatory factors. Recent evidence suggests that during reprogramming, the reprogramming TFs initiate opening of chromatin regions rich in somatic TF motifs that are inaccessible in the initial and final cellular states. It is postulated that analogous to a sponge, these transiently accessible regions "soak up" somatic TFs, hence lowering the initial barriers to cell fate changes. This indirect TF-mediated gene regulation event, which is aptly named the "sponge effect," may play an essential role in the silencing of the somatic transcriptional network during different cellular conversions.

Keywords: cellular reprogramming; decoy DNA; iPSCs; pluripotency; sponge effect; transcription factor; transcription factor sequestration; transiently accessible chromatin regions.