Genomics

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The Demethylase JMJD2C/KDM4C Localizes to H3K4me3 Positive Transcription Start Sites (ChIP-seq KYSE150 cell line)


ABSTRACT: We have mapped binding sites for the histone demethylase, JMJD2C/KDM4C/GASC1, and the effect of JMJD2C depletion on H3K9me3 and H3K36me3 distributions in KYSE150 cells. The human esophageal carcinoma cell line, KYSE150, contains an amplification of the JMJD2C locus. ChIP-seq was performed using chromatin from control or JMJD2C-depleted KYSE150 cells and antibodies recognizing JMJD2C, H3K4me3, H3K9me3 or H3K36me3.

ORGANISM(S): Homo sapiens  

SUBMITTER: Marianne T Pedersen   Marianne Terndrup Pedersen 

PROVIDER: E-GEOD-53938 | ArrayExpress | 2014-01-09

SECONDARY ACCESSION(S): GSE53938SRP035261PRJNA234001

REPOSITORIES: GEO, ArrayExpress, ENA

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Publications

The demethylase JMJD2C localizes to H3K4me3-positive transcription start sites and is dispensable for embryonic development.

Pedersen Marianne Terndrup MT   Agger Karl K   Laugesen Anne A   Johansen Jens V JV   Cloos Paul A C PA   Christensen Jesper J   Helin Kristian K  

Molecular and cellular biology 20140106 6


The histone demethylase JMJD2C, also known as KDM4C/GASC1, has activity against methylated H3K9 and H3K36 and is amplified and/or overexpressed in human cancers. By the generation of Jmjd2c knockout mice, we demonstrate that loss of Jmjd2c is compatible with cellular proliferation, embryonic stem cell (ESC) self-renewal, and embryonic development. Moreover, we report that JMJD2C localizes to H3K4me3-positive transcription start sites in both primary cells and in the human carcinoma KYSE150 cell  ...[more]

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