Pulver, CyrilForey, RomainLederer, Alex R.Begnis, MartinaRosspopoff, OlgaCarlevaro-Fita, JoanaMartins, FilipePlanet, EvaristDuc, JulienRaclot, CharlèneOffner, SandraCoudray, AlexandreDorschel, AriannaTrono, Didier2025-07-022025-07-022025-07-01202510.1016/j.xgen.2025.1009232-s2.0-105008901995https://infoscience.epfl.ch/handle/20.500.14299/251818The cell cycle is a fundamental process in eukaryotic biology and is accordingly controlled by a highly conserved core signaling cascade. However, whether recently evolved proteins also influence this process is unclear. Here, we systematically map the influence of evolutionarily recent transcription factors (TFs) on human cell cycle progression. We find that the genomic targets of select young TFs, many of which belong to the rapidly evolving Krüppel-associated box zinc-finger protein (KZFP) family, exhibit synchronized cell cycle expression. Systematic perturbation studies reveal that silencing recent TFs disrupts normal cell cycle progression, which we experimentally confirm for ZNF519, a simian-restricted KZFP. Furthermore, we show that the therian-specific KZFP ZNF274 sets the cell cycle expression and replication timing of hundreds of clustered genes, many of which are KZFPs. These findings highlight an underappreciated level of lineage specificity in cell cycle regulation.falsecell cycleepigeneticsH3K9me3heterochromatinKRAB zinc-finger proteinsPerturb-seqregulation of transcriptionreplication timingZNF274ZNF519text::journal::journal article::research article