COUP-TFI is a potential regulator of retinoic acid-modulated development in Xenopus embryos

Mech Dev. 1995 May;51(1):39-49. doi: 10.1016/0925-4773(94)00346-o.

Abstract

Isomers of retinoic acid are considered likely regulators of developmental pattern formation in vertebrate embryos. The orphan receptor COUP-TFI, which can alter cellular responses to retinoic acid in cultured cells, is expressed in distinct regions of the developing zebrafish and mouse anterior central nervous system. We asked if COUP-TFI can modulate retinoic acid signaling and anterior neural development in a vertebrate embryo by examining: (1) whether COUP-TFI could alter transcriptional responses to retinoic acid in Xenopus embryonic explants, and (2) whether misexpression of COUP-TFI could regulate anterior neural gene expression during early Xenopus development. The results from these studies show that COUP-TFI is a potent regulator of retinoic acid-induced gene expression in Xenopus embryonic cells, and that misexpression of COUP-TFI causes deficiencies in anterior neural structures and head development in Xenopus embryos with a concomitant change in anterior neural gene expression. These results support the proposition that COUP-TFI has a role in the elaboration and patterning of anterior neural gene expression in vertebrates, possibly via effects on the retinoic acid signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Activins
  • Animals
  • COUP Transcription Factor I
  • Central Nervous System / embryology*
  • Central Nervous System / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology*
  • Embryo, Nonmammalian / metabolism
  • Embryo, Nonmammalian / transplantation
  • Female
  • Gene Expression Regulation, Developmental*
  • Genes, Homeobox
  • Growth Substances / pharmacology
  • In Situ Hybridization
  • Inhibins / pharmacology
  • Male
  • Microinjections
  • Nerve Tissue Proteins / biosynthesis
  • RNA, Messenger / pharmacology
  • Receptors, Glucocorticoid / genetics
  • Receptors, Glucocorticoid / physiology*
  • Sequence Deletion
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • Tretinoin / pharmacology*
  • Xenopus

Substances

  • COUP Transcription Factor I
  • DNA-Binding Proteins
  • Growth Substances
  • Nerve Tissue Proteins
  • RNA, Messenger
  • Receptors, Glucocorticoid
  • Transcription Factors
  • Activins
  • Tretinoin
  • Inhibins