Alterations to the remote control of Shh gene expression cause congenital abnormalities

Philos Trans R Soc Lond B Biol Sci. 2013 May 6;368(1620):20120357. doi: 10.1098/rstb.2012.0357. Print 2013.

Abstract

Multi-species conserved non-coding elements occur in the vertebrate genome and are clustered in the vicinity of developmentally regulated genes. Many are known to act as cis-regulators of transcription and may reside at long distances from the genes they regulate. However, the relationship of conserved sequence to encoded regulatory information and indeed, the mechanism by which these contribute to long-range transcriptional regulation is not well understood. The ZRS, a highly conserved cis-regulator, is a paradigm for such long-range gene regulation. The ZRS acts over approximately 1 Mb to control spatio-temporal expression of Shh in the limb bud and mutations within it result in a number of limb abnormalities, including polydactyly, tibial hypoplasia and syndactyly. We describe the activity of this developmental regulator and discuss a number of mechanisms by which regulatory mutations in this enhancer function to cause congenital abnormalities.

Keywords: Shh; limb development; long-range regulation; preaxial polydactyly.

MeSH terms

  • Animals
  • Binding Sites
  • Congenital Abnormalities / genetics*
  • Congenital Abnormalities / metabolism
  • Conserved Sequence
  • Enhancer Elements, Genetic
  • Evolution, Molecular
  • Gene Expression Regulation, Developmental*
  • Hedgehog Proteins / genetics
  • Hedgehog Proteins / metabolism*
  • Humans
  • Limb Deformities, Congenital / genetics
  • Mutation
  • Transcription, Genetic

Substances

  • Hedgehog Proteins
  • Shh protein, mouse