SETD6 monomethylates H2AZ on lysine 7 and is required for the maintenance of embryonic stem cell self-renewal

Olivier Binda, Ana Sevilla, Gary LeRoy, Ihor R. Lemischka, Benjamin A. Garcia, Stéphane Richard

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The histone H2A variant H2AZ is an essential chromatin signaling factor. Herein, we report that H2AZ is monomethylated at lysine 7 (H2AZK7me1) by the lysine methyltransferase SETD6. We observed that methylation of H2AZ increased noticeably upon cellular differentiation of mouse embryonic stem cells (mESC s). H2AZK7me1 and the repressive H3K27me3 mark were found near the transcriptional start sites of differentiation marker genes, but were removed upon retinoic acid-induced cellular differentiation. The depletion of Setd6 in mESC s led to cellular differentiation, compromised self-renewal, and poor clonogenicity. These findings demonstrate that mESC s require Setd6 for self-renewal and portray H2AZK7me1 as a marker of cellular differentiation. © 2013 Landes Bioscience.
    Original languageEnglish
    Pages (from-to)177-183
    Number of pages6
    JournalEpigenetics: official journal of the DNA Methylation Society
    Volume8
    Issue number2
    DOIs
    Publication statusPublished - 2013

    Keywords

    • Embryonic stem cells
    • H2AZ
    • Histone variant
    • Lysine methylation
    • Lysine methyltransferase
    • SETD6

    Fingerprint

    Dive into the research topics of 'SETD6 monomethylates H2AZ on lysine 7 and is required for the maintenance of embryonic stem cell self-renewal'. Together they form a unique fingerprint.

    Cite this