Omics · study · 2026
Targeting EBF2 condensates modulates adipose thermogenesis
Listed in NCBI GEO
Brown adipose tissue (BAT) actively dissipates energy and represents a promising therapeutic target for combating obesity.
Description
The establishment of the thermogenic gene program is orchestrated by the pioneering transcription factor Early B Cell Factor 2 (EBF2). Here, we identified a low-complexity C-terminal domain (CTD) within EBF2 that drives biomolecular condensation and is essential for thermogenic activation.
Deletion of the CTD (EBF2 ΔCTD) or mutation of key proline residues within this region did not affect the genomic binding of EBF2, but profoundly impaired its ability to undergo phase separation and to drive brown adipocyte differentiation and thermogenic function both in vitro and in vivo. Fusion of the intrinsic disorder region (IDR) of FUS to EBF2 ΔCTD fully restored its function, whereas fusion with MED1-IDR resulted in distinct phenotypic outcomes.
Read the rest (2 more)
Mechanistically, EBF2 formed condensates with ZFP423, a key repressor of brown adipocyte differentiation. This co-condensation excluded HDAC1 from the complex, establishing a permissive chromatin environment that promotes active transcription. Furthermore, a phase separation-based phenotypic drug screen identified compounds that modulated EBF2 condensate formation and thermogenic genes expression.
Our findings reveal phase separation as an emerging regulatory mechanism underlying brown fat determination and suggest that targeting biomolecular condensation offers a novel therapeutic strategy for obesity.
Links
Get the data
- GEO FTP directory ftp.ncbi.nlm.nih.gov/geo/series/GSE297nnn/GSE297178 ↗
download · from NCBI GEO
Where it is published
- GEO accession page ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE297178 ↗
landing page · from NCBI GEO
Documentation and papers
- PRJNA1262940 ncbi.nlm.nih.gov/bioproject/PRJNA1262940 ↗
project · from NCBI GEO
Topics
- Stated by source
- Expression profiling by high throughput sequencing · Genome binding/occupancy profiling by high throughput sequencing · Mus musculus
- From keywords
- Life Sciences
Provenance · 1 source records, 8 field assertions
| Source | Key | Last seen | Raw |
|---|---|---|---|
| NCBI GEO | GSE297178 | 13 d ago | JSON v1 |
| Field | Assertion | Extractor | Evidence |
|---|---|---|---|
| access_level | source · NCBI GEO | connector:ncbi_geo@1.0.0 | |
| concepts[field].local:field:life-sciences | mapping · NCBI GEO | connector:ncbi_geo@1.0.0 | |
| concepts[method].geo_series_type:expression-profiling-by-high-throughput-sequencing | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /gdstype |
| concepts[method].geo_series_type:genome-binding-occupancy-profiling-by-high-throughput-sequencing | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /gdstype |
| concepts[organism].NCBITaxon:10090 | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /taxon |
| description | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /summary |
| publication_date | source · NCBI GEO | connector:ncbi_geo@1.0.0 | |
| title | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /title |