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Series GSE266269 Query DataSets for GSE266269
Status Public on May 06, 2024
Title ENL reads histone β-hydroxybutyrylation to modulate gene transcription (RNA-Seq)
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Histone modifications are typically recognized by chromatin-binding protein modules (referred to as “readers”) to mediate fundamental processes such as transcription. Lysine β-hydroxybutyrylation (Kbhb) is a new type of histone mark that couples metabolism to gene expression. However, the readers that prefer histone Kbhb remain elusive. This knowledge gap must be filled in order to reveal the molecular mechanism of this epigenetic regulation. Herein, we developed a chemical proteomic approach, relying upon multivalent photoaffinity probes to capture binders of the mark and identified ENL as a novel target of H3K9bhb. Biochemical studies and CUT&Tag analysis further suggested that ENL favorably binds to H3K9bhb, and co-localizes with it on promoter regions to modulate gene expression. Notably, disrupting the interaction between H3K9bhb and ENL via structure-based mutation leads to the suppressed expression of the gene like MYC that drives cell proliferation.
 
Overall design we performed RNA-Seq by ectopically expressing WT-ENL or Mutant-ENL in cells
 
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Submission date Apr 30, 2024
Last update date May 06, 2024
Contact name 爱源 王
E-mail(s) way2022@tmu.edu.cn
Phone 15033260249
Organization name TianjinMedical University
Department Department of Biochemistry and Molecular Biology
Lab The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics
Street address No. 22, Meteorological Observatory Road, Heping District, Tianjin
City Tianjin
State/province —Please choose an option—
ZIP/Postal code 300070
Country China
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (2)
GSM8244148 ENL_wt
GSM8244149 ENL_Y78A
Relations
BioProject PRJNA1106487

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE266269_gene_count.xls.gz 2.2 Mb (ftp)(http) XLS
GSE266269_gene_fpkm.xls.gz 2.4 Mb (ftp)(http) XLS
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