Regulation of Maternal Behavior and Offspring Growth by Paternally Expressed Peg3

Author:

Li L.-L.1,Keverne E. B.2,Aparicio S. A.1,Ishino F.3,Barton S. C.1,Surani M. A.1

Affiliation:

1. Wellcome CRC Institute of Cancer and Developmental Biology, and Physiological Laboratory, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK.

2. Sub-Department of Animal Behavior, University of Cambridge, Madingley, Cambridge, UK.

3. Gene Research Center, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226, Japan.

Abstract

Imprinted genes display parent-of-origin–dependent monoallelic expression that apparently regulates complex mammalian traits, including growth and behavior. The Peg3 gene is expressed in embryos and the adult brain from the paternal allele only. A mutation in the Peg3 gene resulted in growth retardation, as well as a striking impairment of maternal behavior that frequently resulted in death of the offspring. This result may be partly due to defective neuronal connectivity, as well as reduced oxytocin neurons in the hypothalamus, because mutant mothers were deficient in milk ejection. This study provides further insights on the evolution of epigenetic regulation of imprinted gene dosage in modulating mammalian growth and behavior.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference38 articles.

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3. B. M. Cattanach and C. V. Beechey in Genomic Imprinting R. Reik and A. Surani Eds. (Oxford Univ. Press New York 1997) pp. 118-141

4. R. Fundele M. Surani N. Allen in Genomic Imprinting R. Reik and A. Surani Eds. (Oxford Univ. Press New York 1997) pp. 98-112.

5. Keverne E. B., Fundele R., Narasimha M., Barton S. C., Surani M. A., Dev. Brain Res. 92, 91 (1996).

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