Highlights d Individual cycling cancer cells display enhanced E2F target gene expression d E2F7/8 deletion or E2F3 overexpression overrides cell-cycle exit after DNA damage d Elevated levels of the E2F target Emi1 prevent DNA-damageinduced cell-cycle exit d The cell-cycle exit after DNA damage is transient and leads to endoreplication

Development, tissue homeostasis and tumor suppression depend critically on the correct regulation of cell division. Central in the cell division process is the decision whether to enter the next cell cycle and commit to going through the S and M phases, or to remain temporarily or permanently arrested. Cell cycle studies in genetic model systems could greatly benefit from visualizing cell cycle commitment in individual cells without the need of fixation. Here, we report the development and characterization of a reporter to monitor cell cycle entry in the nematode C. elegans. This reporter combines the mcm-4 promoter, to reveal Rb/E2F-mediated transcriptional control, and a live-cell sensor for CDK-activity. The CDK sensor was recently developed for use in human cells and consists of a DNA Helicase fragment fused to eGFP. Upon phosphorylation by CDKs, this fusion protein changes in localization from the nucleus to the cytoplasm. The combined regulation of transcription and subcellular localization enabled us to visualize the moment of cell cycle entry in dividing seam cells during C. elegans larval development. This reporter is the first to reflect cell cycle commitment in C. elegans and will help further genetic studies of the mechanisms that underlie cell cycle entry and exit.

Polyploid cells contain more than 2 copies of the genome and are found in many plant and animal tissues. Different types of polyploidy exist, in which the genome is confined to either 1 nucleus (mononucleation) or 2 or more nuclei (multinucleation). Despite the widespread occurrence of polyploidy, the functional significance of different types of polyploidy is largely unknown. Here, we assess the function of multinucleation in Caenorhabditis elegans intestinal cells through specific inhibition of binucleation without altering genome ploidy. Through single-worm RNA sequencing, we find that binucleation is important for tissue-specific gene expression, most prominently for genes that show a rapid up-regulation at the transition from larval development to adulthood. Regulated genes include vitellogenins, which encode yolk proteins that facilitate nutrient transport to the germline. We find that reduced expression of vitellogenins in mononucleated intestinal cells leads to progeny with developmental delays and reduced fitness. Together, our results show that binucleation facilitates rapid up-regulation of intestine-specific gene expression during development, independently of genome ploidy, underscoring the importance of spatial genome organization for polyploid cell function.

E2F transcription factors control the expression of cell cycle genes. Cancers often demonstrate enhanced E2F target gene expression, which can be explained by increased percentages of replicating cells. However, we now demonstrate in human cancer biopsies that individual neoplastic cells display abnormally high levels of E2F-dependent transcription. To mimic this situation, we deleted the atypical E2F repressors (E2F7/8) in untransformed cells. Individual cells with elevated E2F-activity during S/G2-phase failed to exit the cell cycle after DNA damage and underwent mitosis. In contrast, wild type cells completed S-phase and then exit the cell cycle by activating the APC/C Cdh1 via repression of the E2F-target Emi1. Strikingly, many arrested wildtype cells could eventually inactivate APC/C Cdh1 to execute a second round of DNA replication and mitosis, thereby becoming tetraploid. Cells with elevated E2F-transcription fail to exit the cell cycle after DNA damage which potentially causes genomic instability, promotes malignant progression and reduces drug sensitivity.

Chapter 1 systems , such as yeast (Harashima et al. 2013). This box provides a general overview of canonical mitotic cell-cycle regulation. Cell cycle regulationProgression through the cell cycle is primarily regulated through the activity of cyclin-dependent kinases (Cdks), a class of enzymes that initiate the processes of each cell cycle phase (Figure 2a). The activity of Cdks during the cell cycle is regulated by their interaction with cyclins. Cyclins are subject to rapid ubiquitination and degradation at defi ned moments during the cell cycle to regulate their cyclical abundance. The anaphase promoting complex/cyclosome (APC/C) and Skp, Cullin, F-box containing complex (SCF complex) are the two main complexes that regulate the degradation of cyclins and other cell-cycle proteins during the cell cycle (Harashima et al. 2013). An additional layer of cell cycle regulation consists of proteins that aff ect the activity of CDK/cyclin complexes, such as cyclin-dependent kinase inhibitor proteins (CKIs) and CDK or cyclin kinases and phosphatases.