Function and regulation of transcription factors during mitosis-to-G1 transition

Abstract

During cell division, drastic cellular changes characteristic of mitosis result in the inactivation of the transcriptional machinery, and global downregulation of transcription. Sequence-specific transcription factors (TFs) have thus been considered mere bystanders, devoid of any regulatory function during mitosis. This view changed significantly in recent years, upon the conclusion that many TFs associate with condensed chromosomes during cell division, even occupying a fraction of their genomic target sites in mitotic chromatin. This finding was at the origin of the concept of mitotic bookmarking by TFs, proposed as a mechanism to propagate gene regulatory information across cell divisions, by facilitating the reactivation of specific bookmarked genes. While the underlying mechanisms and biological significance of this model remain elusive, recent developments in this fast-moving field have cast new light into TF activity during mitosis, beyond a bookmarking role. Here, we start by reviewing the most recent findings on the complex nature of TF–chromatin interactions during mitosis, and on mechanisms that may regulate them. Next, and in light of recent reports describing how transcription is reinitiated in temporally distinct waves during mitosis-to-G1 transition, we explore how TFs may contribute to defining this hierarchical gene expression process. Finally, we discuss how TF activity during mitotic exit may impact the acquisition of cell identity upon cell division, and propose a model that integrates dynamic changes in TF–chromatin interactions during this cell-cycle period, with the execution of cell-fate decisions.

GATA2 mitotic bookmarking is required for definitive haematopoiesis

“…Nevertheless, lineage-specific transcriptional patterns must be re-established to preserve cell identity after each cell division. Recently, retention of TFs at mitotic chromatin has emerged as a novel mechanism to convey transcriptional memory from mother to daughter cells 4 , 5 . In addition to the ability to decorate mitotic chromatin, several TFs were shown to mark specific genomic sites, a mechanism termed “mitotic bookmarking” 6 – 8 .…”