Trithorax complex component Menin controls differentiation and maintenance of T helper 17 cells

Proc Natl Acad Sci U S A. 2014 Sep 2;111(35):12829-34. doi: 10.1073/pnas.1321245111. Epub 2014 Aug 18.

Abstract

Epigenetic modifications, such as posttranslational modifications of histones, play an important role in gene expression and regulation. These modifications are in part mediated by the Trithorax group (TrxG) complex and the Polycomb group (PcG) complex, which activate and repress transcription, respectively. We herein investigate the role of Menin, a component of the TrxG complex in T helper (Th) cell differentiation and show a critical role for Menin in differentiation and maintenance of Th17 cells. Menin(-/-) T cells do not efficiently differentiate into Th17 cells, leaving Th1 and Th2 cell differentiation intact in in vitro cultures. Menin deficiency resulted in the attenuation of Th17-induced airway inflammation. In differentiating Th17 cells, Menin directly bound to the Il17a gene locus and was required for the deposition of permissive histone modifications and recruitment of the RNA polymerase II transcriptional complex. Interestingly, although Menin bound to the Rorc locus, Menin was dispensable for the induction of Rorc expression and permissive histone modifications in differentiating Th17 cells. In contrast, Menin was required to maintain expression of Rorc in differentiated Th17 cells, indicating that Menin is essential to stabilize expression of the Rorc gene. Thus, Menin orchestrates Th17 cell differentiation and function by regulating both the induction and maintenance of target gene expression.

Keywords: RNAPII; asthma; chromatin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Asthma / immunology*
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Chromatin / immunology
  • Chromatin / metabolism
  • Epigenesis, Genetic / genetics
  • Epigenesis, Genetic / immunology*
  • Gene Expression Regulation / immunology
  • Histone-Lysine N-Methyltransferase / immunology
  • Histone-Lysine N-Methyltransferase / metabolism
  • Interleukin-17 / genetics
  • Interleukin-17 / immunology*
  • Interleukin-17 / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid-Lymphoid Leukemia Protein / immunology
  • Myeloid-Lymphoid Leukemia Protein / metabolism
  • Neutrophils / drug effects
  • Neutrophils / immunology
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / genetics
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / immunology
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • Ovalbumin / immunology
  • Ovalbumin / pharmacology
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / immunology*
  • Proto-Oncogene Proteins / metabolism
  • RNA Polymerase II / immunology
  • RNA Polymerase II / metabolism
  • Th17 Cells / immunology*
  • Th17 Cells / metabolism

Substances

  • Chromatin
  • Il17a protein, mouse
  • Interleukin-17
  • Men1 protein, mouse
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Proto-Oncogene Proteins
  • Rorc protein, mouse
  • Myeloid-Lymphoid Leukemia Protein
  • Ovalbumin
  • Histone-Lysine N-Methyltransferase
  • Kmt2a protein, mouse
  • RNA Polymerase II