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A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [G1E_ChIPseq]

UID: 10880

Author(s): Ludwig, Leif S., Lareau, Caleb A.* * MSK affiliated

Description
Summary from GEO:

"Master regulators, such as the hematopoietic transcription factor GATA1, have numerous roles in lineage commitment and differentiation. While human GATA1 mutations result in several blood diseases, all characterized mutations act relatively early to impair hematopoietic differentiation. Here, we describe a distinct form of hemolytic anemia involving impaired terminal erythropoiesis with a reduced lifespan of circulating red blood cells. We show that this unique blood disorder results from mutations in a poorly characterized and intrinsically disordered C-terminal region of GATA1."

Overall design from GEO:

"Murine G1E cells were transduced with the HMD lentiviral vector encoding HA-tagged human wildtype GATA1 or point mutants p.R307C or p.R307H"
Subject of Study
Subject(s)
Access via GEO


Accession #: GSE133409

Access via BioProject


Accession #: PRJNA551424

Access via SRA


Accession #: SRP212175

Access Restrictions
Free to All
Access Instructions
The NCBI Gene Expression Omnibus, BioProject, and SRA databases provides open access to these files.
Associated Publications
Equipment Used
Dataset Format(s)
TSV, TAR, BED, NARROWPEAK, BW
Dataset Size
2.8 MB (TSV), 2.5 MB (BED), 1023.6 MB (TAR)
Data Catalog Record Updated
2023-10-04