histone methyltransferase

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histone methyltransferase

Targeting histone methyltransferase EZH2 as cancer treatment

The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase

Effect of histone methyltransferase gene mutations on sporulation in S. cerevisiae

Proteome identification of proteins interacting with histone methyltransferase SET8


Histone methyltransferase SETD2 coordinates FACT recruitment with nucleosome dynamics during transcription

Rice SUVH Histone Methyltransferase Genes Display Specific Functions in Chromatin Modification and Retrotransposon Repression

The histone 3 lysine 36 methyltransferase, SET2, is involved in transcriptional elongation

A Histone H3 Lysine-27 Methyltransferase Complex Represses Lateral Root Formation in Arabidopsis thaliana

Histone Lysine Methyltransferase SDG8 Is Involved in Brassinosteroid-Regulated Gene Expression in Arabidopsis thaliana

Novel polymorphisms in the SUV39H2 histone methyltransferase and the risk of lung cancer

Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome

Histone acetyltransferase p300 promotes MKL1-mediated transactivation of catechol-O-methyltransferase gene

Cytoplasmic sequestration of FUS/TLS associated with ALS alters histone marks through loss of nuclear protein arginine methyltransferase 1

FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis

Ectopic Expression of the NtSET1 Histone Methyltransferase Inhibits Cell Expansion, and Affects Cell Division and Differentiation in Tobacco Plants

The phosphatase interactor NIPP1 regulates the occupancy of the histone methyltransferase EZH2 at Polycomb targets

The plasticity of WDR5 peptide-binding cleft enables the binding of the SET1 family of histone methyltransferases


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Euchromatic histone methyltransferase-1 (EHMT1, 1267 aa) is a component of the E2F6 transcriptional repressor and has specificity for core histone H3. Some cases of chromosome 9q subtelomeric deletion syndrome, a mental retardation syndrome, are caused by mutation in the gene for EHMT1. See Jumonji.

Subjects: Medicine and Health.

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