Imprinting centers, chromatin structure, and disease

J Cell Biochem. 2005 May 15;95(2):226-33. doi: 10.1002/jcb.20443.

Abstract

Two regions that best exemplify the role of genetic imprinting in human disease are the Prader-Willi syndrome/Angelman syndrome (PWS/AS) region in 15q11-q13 and the Beckwith-Wiedemann syndrome (BWS) region in 11p15.5. In both regions, cis-acting sequences known as imprinting centers (ICs) regulate parent-specific gene expression bidirectionally over long distances. ICs for both regions are subject to parent-specific epigenetic marking by covalent modification of DNA and histones. In this review, we summarize our current understanding of IC function and IC modification in these two regions.

Publication types

  • Review

MeSH terms

  • Chromatin / chemistry*
  • Genomic Imprinting*
  • Humans
  • Prader-Willi Syndrome / genetics
  • Protein Conformation

Substances

  • Chromatin