Mammalian Genomic Imprinting

  1. Anne C. Ferguson-Smith2
  1. 1Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19063
  2. 2Department of Physiology, Development, and Neuroscience, University of Cambridge, Cambridge, United Kingdom
  1. Correspondence: bartolom{at}mail.med.upenn.edu

Abstract

Normal mammalian development requires a maternal and paternal contribution, which is attributed to imprinted genes, or genes that are expressed from a single parental allele. Approximately 100 imprinted genes have been reported in mammals thus far. Imprinted genes are controlled by cis-acting regulatory elements, termed imprinting control regions (ICRs), which have parental-specific epigenetic modifications, including DNA methylation. ICRs are methylated by de novo DNA methyltransferases during germline development; these parental-specific modifications must be maintained following fertilization when the genome is extensively reprogrammed. Many imprinted genes reside in ∼1-megabase clusters, with two major mechanisms of imprinting regulation currently recognized, CTCF-dependent insulators and long noncoding RNAs. Unclustered imprinted genes are generally regulated by germline-derived differential promoter methylation. Here, we describe the identification and functions of imprinted genes, cis-acting control sequences, trans-acting factors, and imprinting mechanisms in clusters. Finally, we define questions that require more extensive research.



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      1. Cold Spring Harb. Perspect. Biol. 3: a002592 Copyright © 2011 Cold Spring Harbor Laboratory Press; all rights reserved

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