Parent of origin effects
Authors:
- 30 October 2011
- journal article
- review article
- Published by Wiley in Clinical Genetics
- Vol. 81 (3) , 201-209
Abstract
Guilmatre A, Sharp AJ. Parent of origin effects.A major weakness of most genome‐wide association studies has been their inability to fully explain the heritable component of complex disease. Nearly all such studies consider the two parental alleles to be functionally equivalent. However, the existence of imprinted genes demonstrates that this assumption can be wrong. In this review, we describe a wide variety of different mechanisms that underlie many other parent of origin and trans‐generational effects that are known to operate in both humans and model organisms, suggesting that these phenomena are perhaps not uncommon in the genome. We propose that the consideration of alternative models of inheritance will improve our understanding of the heritability and causes of human traits and could have significant impacts on the study of complex disorders.Keywords
This publication has 106 references indexed in Scilit:
- Variation in genome-wide mutation rates within and between human familiesNature Genetics, 2011
- Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypesNature Genetics, 2011
- Paternally Induced Transgenerational Environmental Reprogramming of Metabolic Gene Expression in MammalsCell, 2010
- The Parent-of-Origin of the Extra X Chromosome May Differentially Affect Psychopathology in Klinefelter SyndromeBiological Psychiatry, 2010
- The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetesNature Genetics, 2009
- Finding the missing heritability of complex diseasesNature, 2009
- Variants in nicotinic acetylcholine receptors α5 and α3 increase risks to nicotine dependenceAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2009
- A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of AutismThe American Journal of Human Genetics, 2008
- Dietary protein restriction of pregnant rats in the F0 generation induces altered methylation of hepatic gene promoters in the adult male offspring in the F1 and F2 generationsBritish Journal of Nutrition, 2007
- Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndromeNature Genetics, 2005