Antagonistic coevolution of two imprinted loci with pleiotropic effects - PubMed (original) (raw)
Antagonistic coevolution of two imprinted loci with pleiotropic effects
Jon F Wilkins. Evolution. 2010 Jan.
Abstract
At a locus subject to genomic imprinting, the expression pattern of an allele depends on its parent of origin. Typically, one allele is expressed while the other is transcriptionally silent, and natural selection at the locus will be driven by the inclusive fitness of the active allele. For some aspects of phenotype, the relevant fitness function differs between maternally and paternally derived alleles, so that maternally and paternally expressed imprinted loci become involved in an intragenomic, interlocus conflict. Here I consider the consequences of such a conflict between loci with pleiotropic effects and show that phenotypes are driven away from their optimal values, resulting in a maladaptive, but selectively favored, evolutionary trajectory. The extent to which the evolutionarily stable state departs from the optimal phenotype depends only linearly on the magnitude of the conflict, but is extremely sensitive to the relationship between the pleiotropic effects of the two loci. Thus, even a small intragenomic conflict can have significant deleterious consequences for multiple aspects of phenotype. This result has potential consequences for our understanding of disease states that occur at high frequency in the population, including several common psychological and behavioral disorders such as schizophrenia, bipolar disorder, major depression, and autism.
Similar articles
- Genomic imprinting and conflict-induced decanalization.
Wilkins JF. Wilkins JF. Evolution. 2011 Feb;65(2):537-53. doi: 10.1111/j.1558-5646.2010.01147.x. Epub 2010 Nov 5. Evolution. 2011. PMID: 21029079 - Tissue-specific reactivation of gene expression at an imprinted locus.
Wilkins JF. Wilkins JF. J Theor Biol. 2006 May 21;240(2):277-87. doi: 10.1016/j.jtbi.2005.09.007. Epub 2005 Oct 27. J Theor Biol. 2006. PMID: 16257418 - Diseases associated with genomic imprinting.
Wilkins JF, Úbeda F. Wilkins JF, et al. Prog Mol Biol Transl Sci. 2011;101:401-45. doi: 10.1016/B978-0-12-387685-0.00013-5. Prog Mol Biol Transl Sci. 2011. PMID: 21507360 Review. - Genomic imprinting in Canis familiaris.
Nolan CM, O'Sullivan FM, Brabazon DC, Callanan JJ. Nolan CM, et al. Reprod Domest Anim. 2009 Jul;44 Suppl 2:16-21. doi: 10.1111/j.1439-0531.2009.01387.x. Reprod Domest Anim. 2009. PMID: 19754530 Review. - Competitive signal discrimination, methylation reprogramming and genomic imprinting.
Wilkins JF. Wilkins JF. J Theor Biol. 2006 Oct 7;242(3):643-51. doi: 10.1016/j.jtbi.2006.04.015. Epub 2006 May 9. J Theor Biol. 2006. PMID: 16765385
Cited by
- Sexual selection modulates genetic conflicts and patterns of genomic imprinting.
Faria GS, Varela SA, Gardner A. Faria GS, et al. Evolution. 2017 Mar;71(3):526-540. doi: 10.1111/evo.13153. Epub 2017 Jan 16. Evolution. 2017. PMID: 27991659 Free PMC article. - One hundred years of pleiotropy: a retrospective.
Stearns FW. Stearns FW. Genetics. 2010 Nov;186(3):767-73. doi: 10.1534/genetics.110.122549. Genetics. 2010. PMID: 21062962 Free PMC article. Review. - Intragenomic conflict over bet-hedging.
Wilkins JF, Bhattacharya T. Wilkins JF, et al. Philos Trans R Soc Lond B Biol Sci. 2019 Feb 18;374(1766):20180142. doi: 10.1098/rstb.2018.0142. Philos Trans R Soc Lond B Biol Sci. 2019. PMID: 30966914 Free PMC article. - The geometry of evolutionary conflict.
Rautiala P, Gardner A. Rautiala P, et al. Proc Biol Sci. 2023 Feb 8;290(1992):20222423. doi: 10.1098/rspb.2022.2423. Epub 2023 Feb 8. Proc Biol Sci. 2023. PMID: 36750194 Free PMC article. - Costs and consequences of the conflict over infant sleep.
Wilkins JF. Wilkins JF. Evol Med Public Health. 2014 Jan;2014(1):63-4. doi: 10.1093/emph/eou012. Epub 2014 Mar 14. Evol Med Public Health. 2014. PMID: 24632048 Free PMC article. No abstract available.
MeSH terms
LinkOut - more resources
Full Text Sources