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University of Cambridge

The role of the PWWP domain in the DNA methyltransferase 3A targeting to the genome

Abstract

dc:description.abstract

All cells in a mammalian body share the same DNA content but have a distinct appearance and function. This is achieved by activation and repression of genes by epigenetic mechanisms, which are crucial for stable differentiation of cells in a multi-cellular organism. DNA methylation, established by DNA methyltransferase (DNMT) enzymes, regulates gene expression and is essential for mammalian development. Histone tail post-translational modifications modulate the recruitment and activity of DNMTs. In particular, the PWWP domains of DNMT3A and DNMT3B are posited to interact with histone 3 lysine 36 trimethylation (H3K36me3). In this study, I characterise a mouse model carrying a D329A point mutation in the DNMT3A PWWP domain, predicted to ablate the DNMT3A-PWWP and H3K36me3 interaction. Similar mutations in humans cause primordial dwarfism. I found that oocytes of Dnmt3a-D329A mice show no alterations in DNA methylation. However, the D329A mutation causes dominant postnatal growth retardation in mice. At the molecular level, it results in aberrant progressive acquisition of DNA methylation across domains marked by H3K27me3 and bivalent chromatin in multiple adult tissues. These domains characteristically contain important developmental regulatory genes, and their aberrant methylation is associated with de-repression of these genes in the adult hypothalamus. Recapitulation of this mutation in mouse embryonic stem cells (mESCs) did not identify new DNMT3A-D329A interacting partners. Upon differentiation of Dnmt3a-D329A carrying mESCs to neuronal progenitor cells, a minor gain in DNA methylation is observed. This work provides key molecular insights into the role of DNMT3A in regulating postnatal growth, the targeting of DNMT3A to the genome, function of the DNMT3A PWWP domain and its association with histone modifications.

Degree

thesis:*
Name dc:type.qualificationname
Doctor of Philosophy (PhD)
Level dc:type.qualificationlevel
Doctoral
Grantor dc:publisher.institution
University of Cambridge
Year dc:date.issued
2021

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Sendzikaite, Gintare
Advisor dc:contributor.advisor
  • Kelsey, Gavin

Subjects

dc:subject × 8

Rights

dc:rights
Language dc:language
eng

Identifiers

dc:identifier.*
DOI dc:identifier.doi
https://doi.org/10.17863/CAM.71375
OAI identifier oai:identifier
oai:www.repository.cam.ac.uk:1810/323914

Chain of custody

source
Harvested from
Cambridge University
Base URL
api.repository.cam.ac.uk/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Sendzikaite, Gintare. The role of the PWWP domain in the DNA methyltransferase 3A targeting to the genome. Doctoral thesis, University of Cambridge, 2021. https://doi.org/10.17863/CAM.71375