Polycomb repressive complex 2 regulates normal hematopoietic stem cell function in a developmental-stage-specific manner

Huafeng Xie, Jian Xu, Jessie H. Hsu, Minh Nguyen, Yuko Fujiwara, Cong Peng, Stuart H. Orkin

Research output: Contribution to journalArticle

160 Scopus citations


Recent studies point to a pivotal role of Polycomb repressive complex 2 (PRC2) in stem cell function and cancer. Loss-of-function approaches targeting individual PRC2 subunits have, however, generated findings that are difficult to reconcile. Here, we prevent assembly of both Ezh1- and Ezh2-containing PRC2 complexes by conditional deletion of Eed, a core subunit, and assess hematopoiesis. We find that deletion of Eed exhausts adult bone marrow hematopoietic stem cells (HSCs), although fetal liver HSCs are produced in normal numbers. Eed-null neonatal HSCs express HSC signature genes but are defective in maintenance and differentiation. Comparative gene expression profiling revealed that neonatal and adult HSCs lacking Eed upregulated gene sets of conflicting pathways. Deletion of Cdkn2a, a PRC2 target gene, in Eed-null mice enhances hematopoietic stem/progenitor cell (HSPC) survival but fails to restore HSC functions. Taken together, our findings define developmental-stage-specific requirements for canonical PRC2 complexes in normal HSC function.

Original languageEnglish (US)
Pages (from-to)68-80
Number of pages13
JournalCell Stem Cell
Issue number1
Publication statusPublished - Jan 2 2014


ASJC Scopus subject areas

  • Cell Biology
  • Molecular Medicine
  • Genetics

Cite this