Related Experiment Video
Updated: Jun 7, 2026

09:42
Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
Published on: September 7, 2017
Genomic imprinting and conflict-induced decanalization.
1Santa Fe Institute, Santa Fe, New Mexico 87501, USA. wilkins@santafe.edu
Evolution; International Journal of Organic Evolution
|October 30, 2010
Summary
Genomic imprinting's parental conflict drives gene expression escalation, increasing phenotypic variance and reducing fitness. This conflict-induced decanalization may explain diseases like autism and schizophrenia.
Area of Science:
- Genetics
- Evolutionary Biology
- Developmental Biology
Background:
- Genomic imprinting involves allele expression dependent on parental origin.
- Parental conflict at imprinted loci drives an evolutionary "arms race" for expression levels.
Purpose of the Study:
- To model the consequences of escalating expression at maternally and paternally expressed imprinted loci.
- To investigate the phenomenon of "conflict-induced decanalization" and its impact on population fitness and disease.
Main Methods:
- Theoretical modeling of gene expression dynamics.
- Analysis of selection pressures on imprinted loci and gene expression modifiers.
- Derivation of population-level consequences of genetic conflict.
Main Results:
- Escalation in expression at imprinted loci increases variance in gene expression and phenotypic variance.
- Selection favoring modifiers that canalize gene expression leads to further escalation and net decanalization.
- This feedback loop reduces population mean fitness.
Conclusions:
- Conflict-induced decanalization, driven by genomic imprinting, increases phenotypic variance.
- This process may contribute to the high incidence of diseases including preterm birth, schizophrenia, and autism.
- Understanding this genetic conflict is crucial for explaining disease etiology and evolutionary dynamics.
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...
Epigenetic Regulation
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
X-chromosome...
Epigenetic Regulation
Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
Epigenetic Regulation
Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
Gene Conversion
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Position-effect Variegation
In 1928, a German botanist Emil Heitz observed the moss nuclei with a DNA binding dye. He observed that while some chromatin regions decondense and spread out in the interphase nucleus, others do not. He termed them euchromatin and heterochromatin, respectively. He proposed that the heterochromatin regions reflect a functionally inactive state of the genome. It was later confirmed that heterochromatin is transcriptionally repressed, and euchromatin is transcriptionally active chromatin.
