NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE158736 Query DataSets for GSE158736
Status Public on Feb 28, 2021
Title Complex-dependent histone acetyltransferase activity of KAT8 determines its role in transcriptional regulation and cellular homeostasis (ChIP-sequecing data)
Organisms Homo sapiens; Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary 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.
 
Overall design 39 ChIP-sequencing samples. Where indicated, input or bait KD was used as a control. Where indicated, spike-in normalization factors are provided
 
Contributor(s) Radzisheuskaya A, Helin K
Citation(s) 33657400
Submission date Sep 29, 2020
Last update date Jun 07, 2021
Contact name Aliaksandra Radzisheuskaya
E-mail(s) ar570a@gmail.com
Organization name The Institute of Cancer Research
Department Cancer Biology
Street address 237 Fulham road
City London
ZIP/Postal code SW36JB
Country United Kingdom
 
Platforms (2)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (39)
GSM4809270 ChIP_THP1_WT_aKANSL3
GSM4809271 ChIP_THP1_KANSL3-KD_aKANSL3
GSM4809272 ChIP_THP1_WT_aH3K4me3
Relations
BioProject PRJNA666402
SRA SRP285792

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE158736_ChIP_H3K4me3_peaks.xlsx 751.1 Kb (ftp)(http) XLSX
GSE158736_ChIP_KANSL3_peaks.xlsx 48.0 Kb (ftp)(http) XLSX
GSE158736_ChIP_KAT8_peaks.xlsx 258.8 Kb (ftp)(http) XLSX
GSE158736_RAW.tar 9.5 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap