PXD076443 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | The H3K4 methyltransferase KMT2D is an essential cofactor for GATA1 at erythroid gene enhancers |
| Description | Gene expression during cellular differentiation is coordinated by combinatorial interactions between transcription factors (TFs) and cofactors at promoters and enhancers. The “master TF” GATA1 coordinates gene transcription in a subset of hematopoietic lineages, including erythroid, megakaryocytic, mast, and eosinophil, while repressing the development of other blood lineages. However, the specific cofactors required for GATA1-activated gene expression during hematopoiesis are incompletely defined. We identified the cofactor KMT2D, an H3K4 methyltransferase that collaborates with H3K27 acetyltransferases to activate transcription, in an unbiased CRISPR/Cas9 screen for epigenetic regulators of erythropoiesis. Loss of KMT2D in human erythroid precursors caused developmental arrest with impaired expression of numerous erythroid genes. Mechanistically, KMT2D colocalized with GATA1 on more than one thousand erythroid enhancers associated with over two hundred erythroid genes. In general, co-occupancy of GATA1 and KMT2D at erythroid enhancers was associated with stronger transcriptional activity than occupancy by GATA1 alone. Acute depletion of KMT2D in erythroid precursors caused rapid reductions of H3K4me1 and H3K27ac on a subset of GATA1-bound enhancers and impaired the expression of canonical erythroid genes, including ZFPM1, SLC4A1, and EPOR. Moreover, acute depletion of GATA1 or KMT2D individually caused downregulation of overlapping gene sets. Thus, KMT2D controls erythropoiesis by selectively activating GATA1-dependent erythroid enhancers. Our studies identify KMT2D as a novel cofactor for transcriptional activation by GATA1 during erythropoiesis. More generally, our findings demonstrate how a lineage-specific TF cooperates with a ubiquitous epigenetic regulator to drive lineage-specific gene expression during cellular differentiation. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-04-10 |
| AnnouncementXML | Submission_2026-04-09_18:20:27.772.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Ye Xin |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | LTQ Orbitrap |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2026-04-01 01:06:04 | ID requested | |
| ⏵ 1 | 2026-04-09 18:20:28 | announced | |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: KMT2D |
| GATA1 |
| enhancer |
| transcription regulation |
| hematopoiesis |
| erythropoiesis |
| epigenetics |
Contact List
| Ye Xin |
| contact affiliation | Soochow university, China |
| contact email | 20234053002@stu.suda.edu.cn |
| lab head | |
| Ye Xin |
| contact affiliation | Soochow university |
| contact email | 20234053002@stu.suda.edu.cn |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD076443
- Label: PRIDE project
- Name: The H3K4 methyltransferase KMT2D is an essential cofactor for GATA1 at erythroid gene enhancers