Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Aug 20:13:408.
doi: 10.1186/1471-2164-13-408.

Genomic imprinting and genetic effects on muscle traits in mice

Affiliations

Genomic imprinting and genetic effects on muscle traits in mice

Stefan Kärst et al. BMC Genomics. .

Abstract

Background: Genomic imprinting refers to parent-of-origin dependent gene expression caused by differential DNA methylation of the paternally and maternally derived alleles. Imprinting is increasingly recognized as an important source of variation in complex traits, however, its role in explaining variation in muscle and physiological traits, especially those of commercial value, is largely unknown compared with genetic effects.

Results: We investigated both genetic and genomic imprinting effects on key muscle traits in mice from the Berlin Muscle Mouse population, a key model system to study muscle traits. Using a genome scan, we first identified loci with either imprinting or genetic effects on phenotypic variation. Next, we established the proportion of phenotypic variation explained by additive, dominance and imprinted QTL and characterized the patterns of effects. In total, we identified nine QTL, two of which show large imprinting effects on glycogen content and potential, and body weight. Surprisingly, all imprinting patterns were of the bipolar type, in which the two heterozygotes are different from each other but the homozygotes are not. Most QTL had pleiotropic effects and explained up to 40% of phenotypic variance, with individual imprinted loci accounting for 4-5% of variation alone.

Conclusion: Surprisingly, variation in glycogen content and potential was only modulated by imprinting effects. Further, in contrast to general assumptions, our results show that genomic imprinting can impact physiological traits measured at adult stages and that the expression does not have to follow the patterns of paternal or maternal expression commonly ascribed to imprinting effects.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Imprinting patterns for A) body weight on Mc12.1,B) glycolytic content and C) glycolytic potential on the pleiotropic QTL Mc19.1. The pattern of imprinting effect is bipolar expression for all the traits. We have used uncorrected trait means (i.e. before adjustment for direction of cross and sex) to illustrate the magnitude of effects in this figure.

References

    1. Hager R, Cheverud JM, Wolf JB. Change in maternal environment induced by cross-fostering alters genetic and epigenetic effects on complex traits in mice. Proc Roy Soc B. 2009;276:2949–2954. doi: 10.1098/rspb.2009.0515. - DOI - PMC - PubMed
    1. Bartolomei MS, Ferguson-Smith AC. Mammalian genomic imprinting. Cold Spring Harb Perspect Biol. 2011;3:1–17. - PMC - PubMed
    1. Kelsey G. Epigenetics and the brain: Transcriptome sequencing reveals new depths to genomic imprinting. Bioessays. 2011;33:362–367. doi: 10.1002/bies.201100004. - DOI - PubMed
    1. Thorvaldsen JL, Duran KL, Bartolomei MS. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Gene Dev. 1998;12:3693–3702. doi: 10.1101/gad.12.23.3693. - DOI - PMC - PubMed
    1. Wood AJ, Oakey RJ. Genomic imprinting in mammals: emerging themes and established theories. PLoS Genet. 2006;2:e147. doi: 10.1371/journal.pgen.0020147. - DOI - PMC - PubMed

Publication types

LinkOut - more resources