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Series GSE120557 Query DataSets for GSE120557
Status Public on Nov 26, 2018
Title Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions (mouse RRBS)
Organism Mus musculus
Experiment type Methylation profiling by high throughput sequencing
Summary DNA methylation and Polycomb are key factors in the establishment of vertebrate cellular identity and fate. Here we report de novo missense mutations in DNMT3A, encoding the DNA methyltransferase DNMT3A, that cause microcephalic dwarfism, a hypocellular disorder of extreme global growth failure. Substitutions in the PWWP domain abrogate binding to the histone modifications H3K36me2/3, and alter DNA methylation in patient cells. Polycomb-associated DNA methylation canyons/valleys, hypomethylated domains encompassing developmental genes, become methylated with concomitant depletion of H3K27me3 and H3K4me3 bivalent marks. Such de novo DNA methylation occurs during differentiation of Dnmt3aW326R pluripotent cells in vitro, and is also evident in Dnmt3aW326R/+ dwarf mice. We therefore propose that the interaction of the DNMT3A PWWP domain with H3K36me2/3 normally limits DNA methylation of polycomb-marked regions. Our findings implicate the interplay between DNA methylation and polycomb at key developmental regulators as a determinant of organism size in mammals.
 
Overall design This series contains RRBS from mouse NPC cells and cortex.
 
Contributor(s) Sproul D, Heyn P, Andrew AP
Citation(s) 30478443
Submission date Sep 27, 2018
Last update date Feb 28, 2019
Contact name Duncan Sproul
Organization name University of Edinburgh
Department MRC Human Genetics Unit
Street address Crewe Road South
City Edinburgh
State/province Mid Lothian
ZIP/Postal code EH4 2XU
Country United Kingdom
 
Platforms (1)
GPL21626 NextSeq 550 (Mus musculus)
Samples (13)
GSM3402960 WT_clone_1_NPC (RRBS)
GSM3402961 DNMT3A_homozygous_mutant_clone_1_NPC (RRBS)
GSM3402962 WT_clone_2_NPC (RRBS)
This SubSeries is part of SuperSeries:
GSE120558 Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Relations
BioProject PRJNA493887
SRA SRP162923

Download family Format
SOFT formatted family file(s) SOFTHelp
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE120557_RAW.tar 497.3 Mb (http)(custom) TAR (of BIGWIG, COV)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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