Genomic imprinting in mammals

Cold Spring Harb Perspect Biol. 2014 Feb 1;6(2):a018382. doi: 10.1101/cshperspect.a018382.

Abstract

Genomic imprinting affects a subset of genes in mammals and results in a monoallelic, parental-specific expression pattern. Most of these genes are located in clusters that are regulated through the use of insulators or long noncoding RNAs (lncRNAs). To distinguish the parental alleles, imprinted genes are epigenetically marked in gametes at imprinting control elements through the use of DNA methylation at the very least. Imprinted gene expression is subsequently conferred through lncRNAs, histone modifications, insulators, and higher-order chromatin structure. Such imprints are maintained after fertilization through these mechanisms despite extensive reprogramming of the mammalian genome. Genomic imprinting is an excellent model for understanding mammalian epigenetic regulation.

Publication types

  • Review

MeSH terms

  • Alleles
  • Animals
  • Chromatin / genetics*
  • Chromosomes / genetics
  • DNA Methylation / genetics*
  • Genomic Imprinting / genetics*
  • Histones / genetics*
  • Mammals / genetics*
  • Parents
  • RNA, Long Noncoding / genetics*

Substances

  • Chromatin
  • Histones
  • RNA, Long Noncoding