A dual role for Hox genes in limb anterior-posterior asymmetry

Science. 2004 Jun 11;304(5677):1669-72. doi: 10.1126/science.1096049.

Abstract

Anterior-to-posterior patterning, the process whereby our digits are differently shaped, is a key aspect of limb development. It depends on the localized expression in posterior limb bud of Sonic hedgehog (Shh) and the morphogenetic potential of its diffusing product. By using an inversion of and a large deficiency in the mouse HoxD cluster, we found that a perturbation in the early collinear expression of Hoxd11, Hoxd12, and Hoxd13 in limb buds led to a loss of asymmetry. Ectopic Hox gene expression triggered abnormal Shh transcription, which in turn induced symmetrical expression of Hox genes in digits, thereby generating double posterior limbs. We conclude that early posterior restriction of Hox gene products sets up an anterior-posterior prepattern, which determines the localized activation of Shh. This signal is subsequently translated into digit morphological asymmetry by promoting the late expression of Hoxd genes, two collinear processes relying on opposite genomic topographies, upstream and downstream Shh signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Body Patterning*
  • Chromosome Inversion
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Forelimb / abnormalities
  • Forelimb / embryology*
  • Gene Expression Regulation, Developmental*
  • Gene Targeting
  • Genes, Homeobox*
  • Hedgehog Proteins
  • Heterozygote
  • Hindlimb / abnormalities
  • Hindlimb / embryology
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Homozygote
  • Kruppel-Like Transcription Factors
  • Limb Buds / embryology*
  • Limb Buds / metabolism
  • Mice
  • Morphogenesis
  • Nerve Tissue Proteins*
  • Recombination, Genetic
  • Signal Transduction
  • Toes / abnormalities
  • Toes / embryology
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Zebrafish Proteins
  • Zinc Finger Protein Gli3

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • DNA-Binding Proteins
  • Gli3 protein, mouse
  • Hand2 protein, mouse
  • Hedgehog Proteins
  • Homeodomain Proteins
  • Hoxd11 protein, mouse
  • Hoxd12 protein, mouse
  • Hoxd13 protein, mouse
  • Kruppel-Like Transcription Factors
  • Nerve Tissue Proteins
  • Trans-Activators
  • Transcription Factors
  • Zebrafish Proteins
  • Zinc Finger Protein Gli3
  • hand2 protein, zebrafish