5-hydroxymethylcytosine (5hmC) is a DNA base created during active DNA demethylation by the recently discovered TET enzymes. 5hmC has essential roles in gene expression and differentiation. Here, we demonstrate that 5hmC also localizes to sites of DNA damage and repair. 5hmC accumulates at damage foci induced by aphidicolin and microirradiation and colocalizes with major DNA damage response proteins 53BP1 and γH2AX, revealing 5hmC as an epigenetic marker of DNA damage. Deficiency for the TET enzymes eliminates damage-induced 5hmC accumulation and elicits chromosome segregation defects in response to replication stress. Our results indicate that the TET enzymes and 5hmC play essential roles in ensuring genome integrity.
Details
Title
5-Hydroxymethylcytosine Marks Sites of DNA Damage and Promotes Genome Stability
Authors
Georgia Rose Kafer (Author) - Kyoto University
Xuan Li (Author) - Kyoto University
Takuro Horii (Author) - Gunma University
Isao Suetake (Author) - The University of Osaka
Shoji Tajima (Author) - The University of Osaka
Izuho Hatada (Author) - Gunma University
Peter Mark Carlton (Author) - Kyoto University
Publication details
Cell Reports, Vol.14(6), pp.1283-1292
Publisher
Cell Press
Date published
2016
DOI
10.1016/j.celrep.2016.01.035
ISSN
2211-1247
PMID
26854228
Organisation Unit
School of Health - Biomedicine; Australian Centre for Pacific Islands Research; University of the Sunshine Coast, Queensland; School of Health and Sport Sciences - Legacy; Centre for Bioinnovation; School of Health and Behavioural Sciences - Legacy