Targeted disruption of DNMT1, DNMT3A and DNMT3B in human embryonic stem cells

Jing Liao, Rahul Karnik, Hongcang Gu, Michael J. Ziller, Kendell Clement, Alexander M. Tsankov, Veronika Akopian, Casey A. Gifford, Julie Donaghey, Christina Galonska, Ramona Pop, Deepak Reyon, Shengdar Q. Tsai, William Mallard, J. Keith Joung, John L. Rinn, Andreas Gnirke, Alexander Meissner

Research output: Contribution to journalArticlepeer-review

363 Scopus citations

Abstract

DNA methylation is a key epigenetic modification involved in regulating gene expression and maintaining genomic integrity. Here we inactivated all three catalytically active DNA methyltransferases (DNMTs) in human embryonic stem cells (ESCs) using CRISPR/Cas9 genome editing to further investigate the roles and genomic targets of these enzymes. Disruption of DNMT3A or DNMT3B individually as well as of both enzymes in tandem results in viable, pluripotent cell lines with distinct effects on the DNA methylation landscape, as assessed by whole-genome bisulfite sequencing. Surprisingly, in contrast to findings in mouse, deletion of DNMT1 resulted in rapid cell death in human ESCs. To overcome this immediate lethality, we generated a doxycycline-responsive tTA-DNMT1∗ rescue line and readily obtained homozygous DNMT1-mutant lines. However, doxycycline-mediated repression of exogenous DNMT1∗ initiates rapid, global loss of DNA methylation, followed by extensive cell death. Our data provide a comprehensive characterization of DNMT-mutant ESCs, including single-base genome-wide maps of the targets of these enzymes.

Original languageEnglish
Pages (from-to)469-478
Number of pages10
JournalNature Genetics
Volume47
Issue number5
DOIs
StatePublished - 30 May 2015
Externally publishedYes

Fingerprint

Dive into the research topics of 'Targeted disruption of DNMT1, DNMT3A and DNMT3B in human embryonic stem cells'. Together they form a unique fingerprint.

Cite this