Rinf Regulates Pluripotency Network Genes and Tet Enzymes in Embryonic Stem Cells

Cell Rep. 2019 Aug 20;28(8):1993-2003.e5. doi: 10.1016/j.celrep.2019.07.080.

Abstract

The Retinoid inducible nuclear factor (Rinf), also known as CXXC5, is a nuclear protein, but its functions in the context of the chromatin are poorly defined. We find that in mouse embryonic stem cells (mESCs), Rinf binds to the chromatin and is enriched at promoters and enhancers of Tet1, Tet2, and pluripotency genes. The Rinf-bound regions show significant overlapping occupancy of pluripotency factors Nanog, Oct4, and Sox2, as well as Tet1 and Tet2. We found that Rinf forms a complex with Nanog, Oct4, Tet1, and Tet2 and facilitates their proper recruitment to regulatory regions of pluripotency and Tet genes in ESCs to positively regulate their transcription. Rinf deficiency in ESCs reduces expression of Rinf target genes, including several pluripotency factors and Tet enzymes, and causes aberrant differentiation. Together, our findings establish Rinf as a regulator of the pluripotency network genes and Tet enzymes in ESCs.

Keywords: CXXC5; ESC; Nanog; Rinf; Tet enzymes; pluripotency.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Self Renewal / genetics
  • Chromatin / metabolism
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism*
  • Dioxygenases
  • Enhancer Elements, Genetic / genetics
  • Epigenesis, Genetic
  • Gene Expression Regulation, Developmental*
  • Gene Regulatory Networks*
  • Mice
  • Mice, SCID
  • Mouse Embryonic Stem Cells / metabolism*
  • Nanog Homeobox Protein / metabolism
  • Pluripotent Stem Cells / metabolism*
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins / metabolism
  • Transcription Factors / deficiency
  • Transcription Factors / metabolism*
  • Transcription, Genetic

Substances

  • CXXC5 protein, mouse
  • Chromatin
  • DNA-Binding Proteins
  • Nanog Homeobox Protein
  • Proto-Oncogene Proteins
  • TET1 protein, mouse
  • Transcription Factors
  • Dioxygenases
  • Tet2 protein, mouse