CXXC5 plays a role as a transcription activator for myelin genes on oligodendrocyte differentiation

Glia. 2016 Mar;64(3):350-62. doi: 10.1002/glia.22932. Epub 2015 Oct 14.

Abstract

Myelination in corpus callosum plays important role for normal brain functions by transferring neurological information between various brain regions. However, the factors controlling expression of myelin genes in myelination are poorly understood. Here, CXXC5, a recently identified protein with CXXC-type zinc finger DNA binding motif, was characterized as a transcriptional activator of major myelin genes. We identified expression of CXXC5 expression was increased by Wnt/β-catenin signaling. CXXC5 specifically expressed in the white matter induced expression of myelin genes through the direct binding of CXXC DNA-binding motif of CXXC5 on the MBP promoter. During the differentiation of neural stem cells (NSCs) of CXXC5(-/-) mice, the expressions of myelin genes were simultaneously reduced. The CXXC5(-/-) mice exhibited severely reduction of myelin genes expression in corpus callosum as well as abnormalities in myelin structure. The disrupted structural integrity of myelin in the CXXC5(-/-) mice resulted in reduced electrical conduction amplitudes at corpus callosum. These findings indicate that the regulation of myelin genes expression by CXXC5 is important for forming myelin structure involved with axonal electrical signal transfer in the corpus callosum.

Keywords: CXXC5; Wnt/β-catenin signaling; neural stem cell; oligodendrocyte; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / genetics
  • Animals
  • Animals, Newborn
  • Axons / metabolism
  • Axons / ultrastructure
  • Cell Differentiation / genetics*
  • Cells, Cultured
  • Corpus Callosum / growth & development
  • Corpus Callosum / metabolism
  • DNA-Binding Proteins
  • Embryo, Mammalian
  • Gene Expression Regulation / genetics*
  • Glial Fibrillary Acidic Protein / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Mice, Transgenic
  • Myelin Basic Protein / genetics
  • Myelin Basic Protein / metabolism
  • Myelin Proteolipid Protein / genetics
  • Myelin Proteolipid Protein / metabolism
  • Myelin Sheath / genetics
  • Myelin Sheath / metabolism*
  • Neural Conduction / genetics
  • Neural Stem Cells
  • Oligodendroglia / physiology*
  • Oligodendroglia / ultrastructure
  • Transcription Factors
  • Wnt Signaling Pathway / genetics
  • Wnt3A Protein / pharmacology
  • beta Catenin / metabolism

Substances

  • CXXC5 protein, mouse
  • DNA-Binding Proteins
  • Glial Fibrillary Acidic Protein
  • Intracellular Signaling Peptides and Proteins
  • Myelin Basic Protein
  • Myelin Proteolipid Protein
  • Plp1 protein, mouse
  • Transcription Factors
  • Wnt3A Protein
  • Wnt3a protein, mouse
  • beta Catenin