UHRF1 ubiquitin ligase activity supports the maintenance of low-density CpG methylation Journal Article


Authors: Tiedemann, R. L.; Hrit, J.; Du, Q.; Wiseman, A. K.; Eden, H. E.; Dickson, B. M.; Kong, X.; Chomiak, A. A.; Vaughan, R. M.; Tibben, B. M.; Hebert, J. M.; David, Y.; Zhou, W.; Baylin, S. B.; Jones, P. A.; Clark, S. J.; Rothbart, S. B.
Article Title: UHRF1 ubiquitin ligase activity supports the maintenance of low-density CpG methylation
Abstract: The RING E3 ubiquitin ligase UHRF1 is an established cofactor for DNA methylation inheritance. The model posits that nucleosomal engagement through histone and DNA interactions directs UHRF1 ubiquitin ligase activity toward lysines on histone H3 tails, creating binding sites for DNMT1 through ubiquitin interacting motifs (UIM1 and UIM2). However, the extent to which DNMT1 relies on ubiquitin signaling through UHRF1 in support of DNA methylation maintenance remains unclear. Here, with integrative epigenomic and biochemical analyses, we reveal that DNA methylation maintenance at low-density cytosine-guanine dinucleotides (CpGs) is particularly vulnerable to disruption of UHRF1 ubiquitin ligase activity and DNMT1 ubiquitin reading activity through UIM1. Hypomethylation of low-density CpGs in this manner induces formation of partially methylated domains (PMDs), a methylation signature observed across human cancers. In contrast, UIM2 disruption completely abolishes the DNA methylation maintenance function of DNMT1 in a CpG density-independent manner. In the context of DNA methylation recovery following acute DNMT1 depletion, we further reveal a ‘bookmarking’ function for UHRF1 ubiquitin ligase activity in support of DNA re-methylation. Collectively, these studies show that DNMT1-dependent DNA methylation inheritance is a ubiquitin-regulated process that is partially reliant on UHRF1 and suggest a disrupted UHRF1-DNMT1 ubiquitin signaling axis contributes to PMD formation in cancers. © The Author(s) 2024. Published by Oxford University Press on behalf of Nucleic Acids Research.
Journal Title: Nucleic Acids Research
Volume: 52
Issue: 22
ISSN: 0305-1048
Publisher: Oxford University Press  
Date Published: 2024-12-11
Start Page: 13733
End Page: 13756
Language: English
DOI: 10.1093/nar/gkae1105
PUBMED: 39607687
PROVIDER: scopus
PMCID: PMC11662662
DOI/URL:
Notes: Source: Scopus
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  1. Jakob M Hebert
    5 Hebert