PQBP-1 is expressed predominantly in the central nervous system during development

Eur J Neurosci. 2005 Sep;22(6):1277-86. doi: 10.1111/j.1460-9568.2005.04339.x.

Abstract

Mutations of PQBP-1 (polyglutamine binding protein-1) have been shown recently to cause human mental retardation accompanied by microcephaly at a high frequency. As a first step towards understanding the molecular basis of this developmental anomaly, we analysed developmental expression of PQBP-1 by in situ hybridization, immunohistochemistry and Western blot analysis. Although it had been shown by Northern blot analysis that PQBP-1 mRNA is expressed in multiple organs in adult mice, our present results revealed that PQBP-1 mRNA and protein are dominantly expressed in the central nervous system (CNS) in embryos and in newborn mice. The mean expression level of PQBP-1 reaches a peak around birth and is down-regulated in adulthood. Furthermore, the expression pattern in the CNS changes remarkably following birth. PQBP-1 mRNA in the cerebral cortex is high in embryos but it rapidly decreases after birth. PQBP-1 mRNA increases in external and internal granular cell layers of the cerebellum from postnatal day 1 (P1) to P5. In addition, expression in the subventricular zone, where neurogenesis occurs, was high from P5 to adulthood. Collectively, these findings suggest that PQBP-1 might be involved in neuronal proliferation and/or maturation. These ideas may be relevant to the insufficient growth of brain structure reported in PQBP-1-linked human mental retardation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn / physiology
  • Blotting, Western
  • Brain / growth & development
  • Brain Chemistry / genetics
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Central Nervous System / growth & development*
  • Central Nervous System / metabolism*
  • Cerebral Cortex / metabolism
  • DNA-Binding Proteins
  • Embryo, Mammalian / metabolism
  • Female
  • Glyceraldehyde-3-Phosphate Dehydrogenases / metabolism
  • Immunohistochemistry
  • In Situ Hybridization
  • Mice
  • Mice, Inbred C57BL
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • Oligonucleotides, Antisense / metabolism
  • Pregnancy
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics

Substances

  • Carrier Proteins
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Oligonucleotides, Antisense
  • Pqbp1 protein, mouse
  • RNA, Messenger
  • Glyceraldehyde-3-Phosphate Dehydrogenases