Stag1 and Stag2 regulate cell fate decisions in hematopoiesis through non-redundant topological control [I]

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UID: 11015

Author(s): Viny, Aaron David*, Levine, Ross L.*, Koche, Richard Patrick* * MSK affiliated

Description: Summary from GEO:

"Transcriptional regulators, including the cohesin complex member STAG2, are recurrently mutated in cancer. The role of STAG2 in gene regulation, hematopoiesis, and tumor suppression remains unresolved. We show Stag2 deletion in hematopoietic stem/progenitor cells (HSPC) results in altered hematopoietic function, increased self-renewal, and impaired differentiation. ChIP-sequencing revealed that while Stag2 and Stag1 bind a shared set of genomic loci, a component of Stag2 binding sites are unoccupied by Stag1 even in Stag2-deficient HSPCs. While concurrent loss of Stag2 and Stag1 abrogated hematopoiesis, Stag2 loss alone decreased chromatin accessibility and transcription of lineage-specification genes, including Ebf1 and Pax5, leading to increased self-renewal and reduced HSPC commitment to the B-cell lineage. Our data illustrate a role for Stag2 in transformation and transcriptional dysregulation distinct from its shared role with Stag1 in chromosomal segregation."

Overall design from GEO:

"ChIP-sequencing of PU.1 in Stag2 wildtype and knockout cells derived from murine bone marrow and spleen."

Subject of Study

Subject(s)

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