Genomic imprinting effects on complex traits in domestic animal species
Kaustubh Bhave, Jeevan C, Harshini V and Tilak Pon Jawahar
Mammals are diploid organisms whose cells possess two matched sets of chromosomes, one inherited from the mother and one from the father. Genomic imprinting is an epigenetic mechanism that changes this potential because it restricts the expression of a gene to one of the two parental chromosomes. Monoallelically expressed genes that exert their phenotypic effect in a parent-of-origin speciï¬c manner are considered to be subject to genomic imprinting, the most well understood form of epigenetic regulation of gene expression in mammals. The observed differences in allele speciï¬c gene expression for imprinted genes are not attributable to differences in DNA sequence information, but to speciï¬c chemical modiï¬cations of DNA and chromatin proteins. Since the discovery of genomic imprinting some three decades ago, over 100 imprinted mammalian genes have been identiï¬ed and considerable advances have been made in uncovering the molecular mechanisms regulating imprinted gene expression. While most genomic imprinting studies have focused on mouse models and human biomedical disorders, recent work has highlighted the contributions of imprinted genes to complex trait variation in domestic livestock species. Consequently, greater understanding of genomic imprinting and its effect on agriculturally important traits is predicted to have major implications for the future of animal breeding and husbandry. Imprinted gene expression can have a major effect on phenotypic traits in domestic livestock populations. Furthermore, imprinting is an important factor to consider in the models used for future the genetic improvement of domestic livestock for those genomic regions where imprinted gene expression is known to occur and to affect economically important traits included in the selection index.