E4F1 is a master regulator of CHK1-mediated functions

Cell Rep. 2015 Apr 14;11(2):210-9. doi: 10.1016/j.celrep.2015.03.019. Epub 2015 Apr 2.

Abstract

It has been previously shown that the polycomb protein BMI1 and E4F1 interact physically and genetically in the hematopoietic system. Here, we report that E4f1 is essential for hematopoietic cell function and survival. E4f1 deletion induces acute bone marrow failure characterized by apoptosis of progenitors while stem cells are preserved. E4f1-deficient cells accumulate DNA damage and show defects in progression through S phase and mitosis, revealing a role for E4F1 in cell-cycle progression and genome integrity. Importantly, we showed that E4F1 interacts with and protects the checkpoint kinase 1 (CHK1) protein from degradation. Finally, defects observed in E4f1-deficient cells were fully reversed by ectopic expression of Chek1. Altogether, our results classify E4F1 as a master regulator of CHK1 activity that ensures high fidelity of DNA replication, thus safeguarding genome stability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Bone Marrow / metabolism
  • Bone Marrow / pathology
  • Checkpoint Kinase 1
  • DNA Damage / genetics
  • DNA Replication / genetics
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics*
  • Gene Expression Regulation, Developmental
  • Genomic Instability*
  • HEK293 Cells
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Mice
  • Mouse Embryonic Stem Cells / metabolism
  • Polycomb Repressive Complex 1 / genetics*
  • Polycomb Repressive Complex 1 / metabolism
  • Protein Kinases / biosynthesis*
  • Protein Kinases / genetics
  • Proteolysis
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins / metabolism
  • Repressor Proteins
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics*
  • Ubiquitin-Protein Ligases

Substances

  • Bmi1 protein, mouse
  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Transcription Factors
  • E4f1 protein, mouse
  • Polycomb Repressive Complex 1
  • Ubiquitin-Protein Ligases
  • Protein Kinases
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • Chek1 protein, mouse