Haploinsufficiency of the murine polycomb gene Suz12 results in diverse malformations of the brain and neural tube

Dis Model Mech. 2009 Jul-Aug;2(7-8):412-8. doi: 10.1242/dmm.001602. Epub 2009 Jun 17.

Abstract

Polycomb proteins are epigenetic regulators of gene expression. Human central nervous system (CNS) malformations are congenital defects of the brain and spinal cord. One example of a human CNS malformation is Chiari malformation (CM), which presents as abnormal brainstem growth and cerebellar herniation, sometimes accompanied by spina bifida and cortical defects; it can occur in families. Clinically, CM ranges from an asymptomatic condition to one with incapacitating or lethal symptoms, including neural tube defects and hydrocephalus. However, no genes that are causally involved in any manifestation of CM or similar malformations have been identified. Here, we show that a pathway that involves Zac1 (also known as Plagl1 or Lot1) and controls neuronal proliferation is altered in mice that are heterozygous for the polycomb gene Suz12, resulting in a phenotype that overlaps with some clinical manifestations of the CM spectrum. Suz12 heterozygotes show cerebellar herniation and an enlarged brainstem, accompanied by occipital cortical alterations and spina bifida. Downward displacement of the cerebellum causes hydrocephalus in the most severely impaired cases. Although the involvement of polycomb genes in human disease is starting to be recognized, this is the first demonstration of their role in nervous system malformations. Our work strongly suggests that brain malformations such as CM can result from altered epigenetic regulation of genes involved in cell proliferation in the brain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / abnormalities*
  • Brain / metabolism*
  • Cell Proliferation
  • Epigenesis, Genetic
  • Gene Expression Regulation, Developmental*
  • Heterozygote
  • In Situ Hybridization
  • Mice
  • Models, Genetic
  • Neural Tube Defects / genetics*
  • Phenotype
  • Polycomb Repressive Complex 2
  • Repressor Proteins / genetics*
  • Repressor Proteins / physiology*
  • Time Factors

Substances

  • Repressor Proteins
  • Suz12 protein, mouse
  • Polycomb Repressive Complex 2