Journal
EPIGENETICS
Volume 2, Issue 4, Pages 201-206Publisher
TAYLOR & FRANCIS INC
DOI: 10.4161/epi.2.4.5379
Keywords
androgenetic; Angelman syndrome; behavior; brain; conflict theory; fetal programming; kinship theory; neurodevelopment; parthenoenetic; Prader-Willi syndrome
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As evidence for the existence of brain-expressed imprinted genes accumulates, we need to address exactly what they are doing in this tissue, especially in terms of organizational themes and the major challenges posed by reconciling imprinted gene action in brain with current evolutionary theories attempting to explain the origin and maintenance of genomic imprinting. We are at the beginning of this endeavor and much work remains to be done but already it is clear that imprinted genes have the potential to influence diverse behavioral processes via multiple brain mechanisms. There are also grounds to believe that imprinting may contribute to risk of mental and neurological disease. As well as being a source of basic information about imprinted genes in the brain (e. g., via the newly established website, www.bgg.cardiff.ac.uk/imprinted_tables/index.html), we have used this review to identify and focus on a number of key questions. How are brain-expressed imprinted genes organized at the molecular and cellular levels? To what extent does imprinted action depend on neurodevelopmental mechanisms? Do imprinted gene effects interact with other epigenetic influences, especially early on in life? Are imprinted effects on adult behaviors adaptive or just epiphenomena? If they are adaptive, what areas of brain function and behavior might be sensitive to imprinted effects? These are big questions and, as shall become apparent, we need much more data, arising from interactions between behavioral neuroscientists, molecular biologists and evolutionary theorists, if we are to begin to answer them.
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