Genomic Imprinting and Physiological Processes in Mammals
Author(s) -
Valter Tucci,
Anthony R. Isles,
Gavin Kelsey,
Anne C. FergusonSmith,
Marisa S. Bartolomei,
Nissim Benvenisty,
Déborah Bourc’his,
Marika Charalambous,
Catherine Dulac,
Robert Feil,
Juliane Glaser,
Lisa Huelsmann,
Rosalind M. John,
Gráinne I. McNamara,
Kim Moorwood,
Françoise Muscatelli,
Hiroyuki Sasaki,
Beverly I. Strassmann,
Claudius Vincenz,
Jon F. Wilkins
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.01.043
Subject(s) - genomic imprinting , imprinting (psychology) , biology , epigenetics , genetics , allele , multicellular organism , phenotype , gene , dna methylation , evolutionary biology , gene expression
Complex multicellular organisms, such as mammals, express two complete sets of chromosomes per nucleus, combining the genetic material of both parents. However, epigenetic studies have demonstrated violations to this rule that are necessary for mammalian physiology; the most notable parental allele expression phenomenon is genomic imprinting. With the identification of endogenous imprinted genes, genomic imprinting became well-established as an epigenetic mechanism in which the expression pattern of a parental allele influences phenotypic expression. The expanding study of genomic imprinting is revealing a significant impact on brain functions and associated diseases. Here, we review key milestones in the field of imprinting and discuss mechanisms and systems in which imprinted genes exert a significant role.
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