Defective development of secretory neurones in the hypothalamus of Arnt2-knockout mice

Genes Cells. 2001 Apr;6(4):361-74. doi: 10.1046/j.1365-2443.2001.00421.x.

Abstract

Background: Within the basic region-helix-loop-helix (bHLH)-PAS family of transcription factors, Arnt and Arnt2 play unique roles; these two factors not only heterodimerize with themselves, but also with other members of this family and they act as transcription regulators which bind to specific DNA elements. Whereas Arnt is broadly expressed in various tissues, the expression of Arnt2 is known to be limited to the neural tissues.

Results: To elucidate the function of Arnt2 in detail, we cloned the mouse Arnt2 gene and its gene structure was determined. We subsequently generated germ line Arnt2 mutant mice by gene targeting technology. Heterozygous Arnt2 mice were viable, but homozygous Arnt2 gene knockout mice died shortly after birth. Histological and immunological analyses revealed that the supraoptic nuclei (SON) and the paraventricular nuclei (PVN) are hypocellular. Moreover, secretory neurones identified by the expression of neurosecretory hormone such as arginine vasopressin, oxytocin, corticotrophin-releasing hormone and somatostatin are completely absent in SON and PVN in the mutant Arnt2 mice. Consistent with these observations, prospective SON and PVN neurones which express Brn2 appeared around E13.5 in the mantle zone, but no neurones which expressed the neurosecretory hormones were found in the SON and PVN regions.

Conclusions: These data show that the transcription factor Arnt2 controls the development of the secretory neurones at the later or final stages of differentiation rather than at the beginning stage. Strikingly similar observations have been reported with the Sim1 deficient mice. Taken together, our results demonstrate that Arnt2 is an indispensable transcription factor for the development of the hypothalamus, and suggest that Arnt2 is an obligatory partner molecule of Sim1 in the developmental process of the neuroendocrinological cell lineages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Arginine Vasopressin / metabolism
  • Aryl Hydrocarbon Receptor Nuclear Translocator
  • Base Sequence
  • Basic Helix-Loop-Helix Transcription Factors
  • Corticotropin-Releasing Hormone / metabolism
  • DNA Primers / chemistry
  • Female
  • Gene Deletion
  • Helix-Loop-Helix Motifs / genetics
  • Helix-Loop-Helix Motifs / physiology*
  • Hypothalamus, Anterior / embryology*
  • Hypothalamus, Anterior / metabolism
  • Immunoenzyme Techniques
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Molecular Sequence Data
  • Nerve Tissue Proteins / metabolism
  • Oxytocin / metabolism
  • Paraventricular Hypothalamic Nucleus / embryology
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • Somatostatin / metabolism
  • Supraoptic Nucleus / embryology
  • Supraoptic Nucleus / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • beta-Galactosidase / metabolism

Substances

  • Arnt2 protein, mouse
  • Basic Helix-Loop-Helix Transcription Factors
  • DNA Primers
  • Nerve Tissue Proteins
  • RNA, Messenger
  • Transcription Factors
  • Arginine Vasopressin
  • Aryl Hydrocarbon Receptor Nuclear Translocator
  • Oxytocin
  • Somatostatin
  • Corticotropin-Releasing Hormone
  • beta-Galactosidase