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Molecular Genetics of Genomic Imprinting
Nucleic Acids
Published Online: 10 OCT 2011
DOI: 10.1002/3527600906.mcb.200300031.pub2
Copyright © 2006 Wiley-VCH Verlag GmbH & Co. KGaA. All rights reserved.
Book Title

Reviews in Cell Biology and Molecular Medicine
Additional Information
How to Cite
Hirasawa, R., Kota, S. K. and Feil, R. 2011. Molecular Genetics of Genomic Imprinting. Reviews in Cell Biology and Molecular Medicine. .
Publication History
- Published Online: 10 OCT 2011
Abstract
Genomic imprinting is a developmental mechanism in placental mammals leading to the repression or expression of genes, depending on whether they are inherited from the mother or the father. The imprinted expression of genes is regulated by various epigenetic alterations, including DNA methylation and covalent modifications on histones. A large number of imprinted genes have been identified. Mostly organized in gene clusters in the genome, imprinted genes play important roles in embryonic and extraembryonic development, and in behavior. In humans, genetic and epigenetic alterations at imprinted gene clusters are involved in different disease syndromes, and in cancer.
Keywords:
- Androgenetic embryo;
- Chromatin;
- DNA methylation;
- Gynogenetic embryo;
- Genomic imprinting;
- Histone modification;
- Imprinting and behavior;
- Imprinting and growth;
- Imprinting control regions (ICRs);
- Long noncoding RNAs;
- Nucleosome;
- Parthenogenesis;
- Primordial germ cells (PGCs);
- Uniparental disomy (UPD)
