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Updated: Jun 28, 2026

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Assessment of Sexual Behavior of Male Mice
Published on: March 5, 2020
Sex dependent imprinting effects on complex traits in mice
Reinmar Hager1, James M Cheverud, Larry J Leamy
1Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK. reinmar.hager@cantab.net
BMC Evolutionary Biology
|November 4, 2008
Summary
This study reveals that genomic imprinting effects can be sex-dependent, impacting complex traits differently in males and females. Researchers identified 13 loci with sex-specific imprinting, advancing our understanding of epigenetic variation.
Area of Science:
- Genetics
- Epigenetics
- Quantitative Trait Loci (QTL) Analysis
Background:
- Genomic imprinting is an epigenetic mechanism causing monoallelic gene expression.
- Imprinting influences complex traits across species, but its sex-dependence is unexplored.
- Previous research noted sex-dependent genetic effects, but not sex-dependent imprinting effects.
Purpose of the Study:
- To investigate sex-dependent genomic imprinting effects on complex traits.
- To empirically assess theoretical predictions on the evolution of sex-dependent imprinting.
- To identify loci exhibiting sex-specific imprinting.
Main Methods:
- Genome-wide scan in an intercross between two divergent mouse strains.
- Analysis of complex growth and body composition traits.
- Detection of sex-specific differences in imprinting effects.
Main Results:
- First evidence for sex-dependent genomic imprinting effects, independent of sex chromosomes.
- Identified 13 loci on 11 chromosomes with sex-specific imprinting.
- Most loci showed imprinting in only one sex (8 in males, 6 in females); one locus was sex-dependent for different traits in both sexes.
Conclusions:
- Genomic imprinting effects can be sex-dependent.
- Sex-specific imprinting analysis can reveal novel imprinted loci.
- Current data do not fully support evolutionary predictions; further research on selection pressures is needed.
Related Concept Videos
Genomic Imprinting and Inheritance
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
X-linked Traits
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
X-linked Traits
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
Dosage Compensation
In animals, gender is determined by the number and type of sex chromosome. For example, human females have two X chromosomes, and males have one X and one Y chromosome, whereas C.elegans with one X chromosome is a male, and the one with two X chromosomes is a hermaphrodite.
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with distinct numbers of X chromosomes will have...
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with distinct numbers of X chromosomes will have...
Background and Environment Affect Phenotype
Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as temperature, oxygen availability, presence of mutagens, that can alter an organism’s phenotype.
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
X-Inactivation
The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, one might expect females to produce twice as many of the proteins, with undesirable results.

