PXD023865 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Complex-dependent histone acetyltransferase activity of KAT8 determines its role in transcriptional regulation and cellular homeostasis [TMT11plex whole proteome analysis] |
| Description | Histone acetylation is associated with open chromatin and transcriptionally active genes. Specifically, acetylation of lysine 16 on histone H4 (H4K16ac) has been shown to prevent the assembly of nucleosomal arrays in vitro. This modification is catalyzed by the MYST-family histone acetyltransferase KAT8 (also known as MOF and MYST1), which is part of two distinct chromatin-associated complexes: NSL and MSL. While extensively studied in Drosophila, the functions of H4K16ac and the two KAT8-containing complexes in mammalian cells are not well understood. Here, we demonstrate a surprising complex-dependent activity of KAT8. We found that KAT8 catalyzes H4K5 and H4K8 acetylation as part of the NSL complex, whereas it catalyzes the bulk of H4K16 acetylation as part of the MSL complex. Furthermore, we show that the core proteins of the MSL complex and H4K16ac are not required for cell proliferation and global chromatin accessibility, whereas the NSL complex is essential for cell survival, as it is enriched at the promoters of housekeeping genes and is required for their transcription initiation. In summary, we show that KAT8 switches catalytic activity and function depending on its associated proteins, and that, as part of the NSL complex, it catalyzes H4K5 and H4K8 acetylation required for the expression of genes essential for cell survival |
| HostingRepository | PRIDE |
| AnnounceDate | 2021-06-29 |
| AnnouncementXML | Submission_2021-06-29_10:19:58.828.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Pavel Shliaha |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
| ModificationList | TMT6plex-126 reporter+balance reagent acylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Fusion Lumos |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2021-01-28 04:05:56 | ID requested | |
| ⏵ 1 | 2021-06-29 10:19:59 | announced | |
| 2 | 2021-06-29 21:09:42 | announced | 2021-06-30: Updated publication reference for PubMed record(s): 33657400. |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: histone, MSL, NSL, KAT8 |
Contact List
| Ole N Jensen |
| contact affiliation | University of Southern Denmark, Department of Biochemistryand Molecular Biology, Protein Research Group (lab head) |
| contact email | jenseno@bmb.sdu.dk |
| lab head | |
| Pavel Shliaha |
| contact affiliation | Syddansk University |
| contact email | pavels@bmb.sdu.dk |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD023865
- Label: PRIDE project
- Name: Complex-dependent histone acetyltransferase activity of KAT8 determines its role in transcriptional regulation and cellular homeostasis [TMT11plex whole proteome analysis]