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The Saccharomyces cerevisiae Set1 complex includes an Ash2 homologue and methylates histone 3 lysine 4
- Source :
- The EMBO Journal. 20:7137-7148
- Publication Year :
- 2001
- Publisher :
- Wiley, 2001.
-
Abstract
- The SET domain proteins, SUV39 and G9a have recently been shown to be histone methyltransferases specific for lysines 9 and 27 (G9a only) of histone 3 (H3). The SET domains of the Saccharomyces cerevisiae Set1 and Drosophila trithorax proteins are closely related to each other but distinct from SUV39 and G9a. We characterized the complex associated with Set1 and Set1C and found that it is comprised of eight members, one of which, Bre2, is homologous to the trithorax-group (trxG) protein, Ash2. Set1C requires Set1 for complex integrity and mutation of Set1 and Set1C components shortens telomeres. One Set1C member, Swd2/Cpf10 is also present in cleavage polyadenylation factor (CPF). Set1C methylates lysine 4 of H3, thus adding a new specificity and a new subclass of SET domain proteins known to methyltransferases. Since methylation of H3 lysine 4 is widespread in eukaryotes, we screened the databases and found other Set1 homologues. We propose that eukaryotic Set1Cs are H3 lysine 4 methyltransferases and are related to trxG action through association with Ash2 homologues.
- Subjects :
- Histone H3 Lysine 4
Saccharomyces cerevisiae Proteins
Methyltransferase
Molecular Sequence Data
Saccharomyces cerevisiae
Histone H2B ubiquitination
Biology
Methylation
Article
General Biochemistry, Genetics and Molecular Biology
Histones
Amino Acid Sequence
Histone methyltransferase complex
Molecular Biology
DNA Primers
Base Sequence
Sequence Homology, Amino Acid
General Immunology and Microbiology
Lysine
General Neuroscience
Histone-Lysine N-Methyltransferase
biology.organism_classification
DNA-Binding Proteins
Blotting, Southern
Histone
Biochemistry
Histone methyltransferase
biology.protein
Transcription Factors
Subjects
Details
- ISSN :
- 14602075
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- The EMBO Journal
- Accession number :
- edsair.doi.dedup.....74597779f6119add4a22b0e398c9d8d1
- Full Text :
- https://doi.org/10.1093/emboj/20.24.7137