DNA Methylation Dynamics and Dysregulation Delineated by High-Throughput Profiling in the Mouse

Author:

Zhou Wanding,Hinoue Toshinori,Barnes Bret,Mitchell Owen,Iqbal Waleed,Lee Sol Moe,Foy Kelly K.,Lee Kwang-Ho,Moyer Ethan J.,VanderArk Alexandra,Koeman Julie M.,Ding Wubin,Kalkat Manpreet,Spix Nathan J.,Eagleson Bryn,Pospisilik John Andrew,Szabó Piroska E.ORCID,Bartolomei Marisa S.ORCID,Vander Schaaf Nicole A.,Kang Liang,Wiseman Ashley K.,Jones Peter A.,Krawczyk Connie M.,Adams Marie,Porecha Rishi,Chen Brian H.,Shen Hui,Laird Peter W.ORCID

Abstract

SUMMARYWe have developed a mouse Infinium DNA methylation array that contains 297,415 probes to capture the diversity of mouse DNA methylation biology. We present a mouse DNA methylation atlas as a rich reference resource of 1,239 DNA samples encompassing distinct tissues, strains, age, sex, and pathologies. We describe applications for comparative epigenomics, genomic imprinting, epigenetic inhibitors, PDX assessment, backcross tracing, and epigenetic clocks. We dissect DNA methylation processes associated with differentiation, aging and tumorigenesis. Notably, we find that tissue-specific methylation signatures localize to binding sites for transcription factors controlling the corresponding tissue development. Age-associated hypermethylation is enriched at regions of Polycomb repression, while hypomethylation is enhanced at regions bound by cohesin complex members. ApcMin/+ polyp-associated hypermethylation affects enhancers regulating intestinal differentiation, while hypomethylation targets AP-1 binding sites. This MM285 mouse array is widely accessible to the research community, and will accelerate future high sample-throughput studies in this important model organism.

Publisher

Cold Spring Harbor Laboratory

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