Thyroid hormone-dependent gene expression program for Xenopus neural development

J Biol Chem. 1997 Mar 28;272(13):8179-88. doi: 10.1074/jbc.272.13.8179.

Abstract

Although thyroid hormone (TH) plays a significant role in vertebrate neural development, the molecular basis of TH action on the brain is poorly understood. Using polymerase chain reaction-based subtractive hybridization we isolated 34 cDNAs for TH-regulated genes in the diencephalon of Xenopus tadpoles. Northern blots verified that the mRNAs are regulated by TH and are expressed during metamorphosis. Kinetic analyses showed that most of the genes are up-regulated by TH within 4-8 h and 13 are regulated by TH only in the brain. All cDNA fragments were sequenced and the identities of seven were determined through homology with known genes; an additional five TH-regulated genes were identified by hybridization with known cDNA clones. These include five transcription factors (including two members of the steroid receptor superfamily), a TH-converting deiodinase, two metabolic enzymes, a protein disulfide isomerase-like protein that may bind TH, a neural-specific cytoskeletal protein, and two hypophysiotropic neuropeptides. This is the first successful attempt to isolate a large number of TH-target genes in the developing vertebrate brain. The gene identities allow predictions about the gene regulatory networks underlying TH action on the brain, and the cloned cDNAs provide tools for understanding the basic molecular mechanisms underlying neural cell differentiation.

MeSH terms

  • Animals
  • Blotting, Southern
  • Brain / growth & development*
  • DNA, Complementary / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Diencephalon / chemistry
  • Diencephalon / growth & development
  • Down-Regulation
  • Gene Expression Regulation, Developmental*
  • Kinetics
  • Protein Biosynthesis
  • RNA, Messenger / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Triiodothyronine / genetics
  • Triiodothyronine / physiology*
  • Up-Regulation
  • Xenopus Proteins*
  • Xenopus laevis
  • Zinc Fingers

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • KLF9 protein, Xenopus
  • RNA, Messenger
  • Transcription Factors
  • Xenopus Proteins
  • Triiodothyronine