RT Journal Article SR Electronic T1 Replication timing analysis in polyploid cells reveals Rif1 uses multiple mechanisms to promote underreplication in Drosophila JF bioRxiv FD Cold Spring Harbor Laboratory SP 2021.04.19.440528 DO 10.1101/2021.04.19.440528 A1 Souradip Das A1 Madison Caballero A1 Tatyana Kolesnikova A1 Igor Zhimulev A1 Amnon Koren A1 Jared Nordman YR 2021 UL http://biorxiv.org/content/early/2021/04/19/2021.04.19.440528.abstract AB Regulation of DNA replication and copy number are necessary to promote genome stability and maintain cell and tissue function. DNA replication is regulated temporally in a process known as replication timing (RT). Rif1 is key regulator of RT and has a critical function in copy number control in polyploid cells. In a previous study (Munden et al., 2018), we demonstrated that Rif1 functions with SUUR to inhibit replication fork progression and promote underreplication (UR) of specific genomic regions. How Rif1-dependent control of RT factors into its ability to promote UR is unknown. By applying a computational approach to measure RT in Drosophila polyploid cells, we show that SUUR and Rif1 have differential roles in controlling UR and RT. Our findings reveal that Rif1 functions both upstream and downstream of SUUR to promote UR. Our work provides new mechanistic insight into the process of UR and its links to RT.Competing Interest StatementThe authors have declared no competing interest.