Selected imprinting of INS in the marsupial
1 ARC Centre of Excellence in Kangaroo Genomics, University of Melbourne, Melbourne, Victoria, 3010, Australia
2 Department of Zoology, The University of Melbourne, Melbourne, Victoria, 3010, Australia
3 Epigenomics Division, Frontier Agriscience and Technology Center, Faculty of Agriculture, Shinshu University, Nagano, 399-4598, Japan
4 Department of Molecular and Cellular Biology, The University of Connecticut, Storrs, Connecticut, CT06269, USA
Epigenetics & Chromatin 2012, 5:14 doi:10.1186/1756-8935-5-14Published: 28 August 2012
In marsupials, growth and development of the young occur postnatally, regulated by milk that changes in composition throughout the long lactation. To initiate lactation in mammals, there is an absolute requirement for insulin (INS), a gene known to be imprinted in the placenta. We therefore examined whether INS is imprinted in the mammary gland of the marsupial tammar wallaby (Macropus eugenii) and compared its expression with that of insulin-like growth factor 2 (IGF2).
INS was expressed in the mammary gland and significantly increased, while IGF2 decreased, during established milk production. Insulin and IGF2 were both detected in the mammary gland macrophage cells during early lactation and in the alveolar cells later in lactation. Surprisingly, INS, which was thought only to be imprinted in the therian yolk sac, was imprinted and paternally expressed in the liver of the developing young, monoallelically expressed in the tammar mammary gland and biallelic in the stomach and intestine. The INS transcription start site used in the liver and mammary gland was differentially methylated.
This is the first study to identify tissue-specific INS imprinting outside the yolk sac. These data suggest that there may be an advantage of selective monoallelic expression in the mammary gland and that this may influence the growth of the postnatal young. These results are not consistent with the parental conflict hypothesis, but instead provide support for the maternal–infant co-adaptation hypothesis. Thus, imprinting in the mammary gland maybe as critical for postnatal growth and development in mammals as genomic imprinting in the placenta is prenatally.