Rif1 Is Required for Resolution of Ultrafine DNA Bridges in Anaphase to Ensure Genomic Stability

Publication date

2015-08-24

Authors

Hengeveld, Rutger C CISNI 0000000397064918
Schoonen, Pepijn M
de Vries, Elisabeth G E
Lens, SusanneORCID 0000-0003-2199-7594ISNI 0000000392875244
van Vugt, Marcel A T M

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taverne

Abstract

Sister-chromatid disjunction in anaphase requires the resolution of DNA catenanes by topoisomerase II together with Plk1-interacting checkpoint helicase (PICH) and Bloom's helicase (BLM). We here identify Rif1 as a factor involved in the resolution of DNA catenanes that are visible as ultrafine DNA bridges (UFBs) in anaphase to which PICH and BLM localize. Rif1, which during interphase functions downstream of 53BP1 in DNA repair, is recruited to UFBs in a PICH-dependent fashion, but independently of 53BP1 or BLM. Similar to PICH and BLM, Rif1 promotes the resolution of UFBs: its depletion increases the frequency of nucleoplasmic bridges and RPA70-positive UFBs in late anaphase. Moreover, in the absence of Rif1, PICH, or BLM, more nuclear bodies with damaged DNA arise in ensuing G1 cells, when chromosome decatenation is impaired. Our data reveal a thus far unrecognized function for Rif1 in the resolution of UFBs during anaphase to protect genomic integrity.

Keywords

Anaphase, CDC2 Protein Kinase, Chromatids, DNA, DNA Damage, G1 Phase, Genomic Instability, HeLa Cells, Humans, MCF-7 Cells, Micronucleus, Germline, Protein Transport, Telomere-Binding Proteins, Taverne, Journal Article, Research Support, Non-U.S. Gov't

Citation

Hengeveld, R C C, Schoonen, P M, de Vries, E G E, Lens, S M A & van Vugt, M A T M 2015, 'Rif1 Is Required for Resolution of Ultrafine DNA Bridges in Anaphase to Ensure Genomic Stability', Developmental Cell, vol. 34, no. 4, pp. 466-474. https://doi.org/10.1016/j.devcel.2015.06.014