Mutations in gene regulatory elements linked to human limb malformations

J Med Genet. 2020 Jun;57(6):361-370. doi: 10.1136/jmedgenet-2019-106369. Epub 2019 Dec 19.

Abstract

Most of the human genome has a regulatory function in gene expression. The technological progress made in recent years permitted the revision of old and discovery of new mutations outside of the protein-coding regions that do affect human limb morphology. Steadily increasing discovery rate of such mutations suggests that until now the largely neglected part of the genome rises to its well-deserved prominence. In this review, we describe the recent technological advances permitting this unprecedented advance in identifying non-coding mutations. We especially focus on the mutations in cis-regulatory elements such as enhancers, and trans-regulatory elements such as miRNA and long non-coding RNA, linked to hereditary or inborn limb defects. We also discuss the role of chromatin organisation and enhancer-promoter interactions in the aetiology of limb malformations.

Keywords: enhancers; limb defects; lncRNA; miRNA; non-coding DNA.

Publication types

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

MeSH terms

  • Extremities / growth & development
  • Gene Expression Regulation / genetics
  • Gene Regulatory Networks / genetics
  • Genome, Human / genetics
  • Humans
  • Limb Deformities, Congenital / genetics*
  • Limb Deformities, Congenital / pathology
  • MicroRNAs / genetics*
  • RNA, Long Noncoding / genetics*

Substances

  • MicroRNAs
  • RNA, Long Noncoding