H3K14 ubiquitylation promotes H3K9 methylation for heterochromatin assembly. (29th August 2019)
- Record Type:
- Journal Article
- Title:
- H3K14 ubiquitylation promotes H3K9 methylation for heterochromatin assembly. (29th August 2019)
- Main Title:
- H3K14 ubiquitylation promotes H3K9 methylation for heterochromatin assembly
- Authors:
- Oya, Eriko
Nakagawa, Reiko
Yoshimura, Yuriko
Tanaka, Mayo
Nishibuchi, Gohei
Machida, Shinichi
Shirai, Atsuko
Ekwall, Karl
Kurumizaka, Hitoshi
Tagami, Hideaki
Nakayama, Jun‐ichi - Abstract:
- Abstract: The methylation of histone H3 at lysine 9 (H3K9me), performed by the methyltransferase Clr4/SUV39H, is a key event in heterochromatin assembly. In fission yeast, Clr4, together with the ubiquitin E3 ligase Cul4, forms the Clr4 methyltransferase complex (CLRC), whose physiological targets and biological role are currently unclear. Here, we show that CLRC‐dependent H3 ubiquitylation regulates Clr4's methyltransferase activity. Affinity‐purified CLRC ubiquitylates histone H3, and mass spectrometric and mutation analyses reveal that H3 lysine 14 (H3K14) is the preferred target of the complex. Chromatin immunoprecipitation analysis shows that H3K14 ubiquitylation (H3K14ub) is closely associated with H3K9me‐enriched chromatin. Notably, the CLRC‐mediated H3 ubiquitylation promotes H3K9me by Clr4, suggesting that H3 ubiquitylation is intimately linked to the establishment and/or maintenance of H3K9me. These findings demonstrate a cross‐talk mechanism between histone ubiquitylation and methylation that is involved in heterochromatin assembly. Synopsis: The Clr4 methyltransferase complex in fission yeast preferentially ubiquitylates H3K14. H3K14ub is linked to H3K9me‐enriched heterochromatin and promotes Clr4 methyltransferase activity. The Clr4 methyltransferase complex (CLRC) preferentially ubiquitylates H3K14. K14‐ubiquitylated histone H3 is enriched in heterochromatin. CLRC‐mediated H3 ubiquitylation promotes Clr4 methyltransferase activity. Abstract : The Clr4Abstract: The methylation of histone H3 at lysine 9 (H3K9me), performed by the methyltransferase Clr4/SUV39H, is a key event in heterochromatin assembly. In fission yeast, Clr4, together with the ubiquitin E3 ligase Cul4, forms the Clr4 methyltransferase complex (CLRC), whose physiological targets and biological role are currently unclear. Here, we show that CLRC‐dependent H3 ubiquitylation regulates Clr4's methyltransferase activity. Affinity‐purified CLRC ubiquitylates histone H3, and mass spectrometric and mutation analyses reveal that H3 lysine 14 (H3K14) is the preferred target of the complex. Chromatin immunoprecipitation analysis shows that H3K14 ubiquitylation (H3K14ub) is closely associated with H3K9me‐enriched chromatin. Notably, the CLRC‐mediated H3 ubiquitylation promotes H3K9me by Clr4, suggesting that H3 ubiquitylation is intimately linked to the establishment and/or maintenance of H3K9me. These findings demonstrate a cross‐talk mechanism between histone ubiquitylation and methylation that is involved in heterochromatin assembly. Synopsis: The Clr4 methyltransferase complex in fission yeast preferentially ubiquitylates H3K14. H3K14ub is linked to H3K9me‐enriched heterochromatin and promotes Clr4 methyltransferase activity. The Clr4 methyltransferase complex (CLRC) preferentially ubiquitylates H3K14. K14‐ubiquitylated histone H3 is enriched in heterochromatin. CLRC‐mediated H3 ubiquitylation promotes Clr4 methyltransferase activity. Abstract : The Clr4 methyltransferase complex in fission yeast preferentially ubiquitylates H3K14. H3K14ub is linked to H3K9me‐enriched heterochromatin and promotes Clr4 methyltransferase activity. … (more)
- Is Part Of:
- EMBO reports. Volume 20:Number 10(2019)
- Journal:
- EMBO reports
- Issue:
- Volume 20:Number 10(2019)
- Issue Display:
- Volume 20, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 20
- Issue:
- 10
- Issue Sort Value:
- 2019-0020-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-08-29
- Subjects:
- epigenetic gene silencing -- fission yeast -- heterochromatin -- histone methylation -- histone ubiquitylation
Molecular biology -- Periodicals
Molecular Biology -- Periodicals
Molecular biology
Periodicals
572.8 - Journal URLs:
- http://www.embo-reports.oupjournals.org/ ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1469-221x;screen=info;ECOIP ↗ - DOI:
- 10.15252/embr.201948111 ↗
- Languages:
- English
- ISSNs:
- 1469-221X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3733.086000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24630.xml