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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.
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Behavioral imprinting is observed in some newborn animals and occurs when they develop strong and specific attachments to another animal (usually a parent) following brief, early-life exposures. Offspring imprint onto parents within a brief period after birth or hatching; this time window is called the critical period. Once imprinting occurs, the bond established between the parents and their offspring is usually long-lasting.
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Related Experiment Video

Updated: Feb 3, 2026

Using Caenorhabditis elegans for Studying Trans- and Multi-Generational Effects of Toxicants
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Trans-allelic mutational effects at the Peg3 imprinted locus.

Corey L Bretz1, Joomyeong Kim1

  • 1Department of Biological Sciences, Louisiana State University, Baton Rouge, LA, United States of America.

Plos One
|October 19, 2018
PubMed
Summary

This study reveals novel allele interactions at the Peg3 imprinted locus. Maternal deletion of the Peg3-DMR up-regulates paternally expressed genes, showing unidirectional regulation.

Area of Science:

  • Genetics
  • Molecular Biology
  • Developmental Biology

Background:

  • Allelic interactions are crucial for gene function but not fully understood.
  • The Peg3 imprinted locus is a key area for studying gene regulation.

Purpose of the Study:

  • To investigate trans-allelic interactions at the Peg3 imprinted locus.
  • To determine the role of the Peg3 Imprinting Control Region (Peg3-DMR) in gene regulation.

Main Methods:

  • Utilized mutant alleles targeting the Peg3-DMR.
  • Analyzed gene expression of paternally expressed genes (Peg3, Usp29) in various tissues and developmental stages.

Main Results:

  • Maternal deletion of Peg3-DMR caused a 2-fold upregulation of Peg3 and Usp29.

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  • These effects were consistent across tissues and developmental stages.
  • The observed trans-allelic effects were unidirectional, with maternal influence on the paternal allele.
  • Conclusions:

    • Identified previously unrecognized trans-allelic regulation associated with the Peg3-DMR.
    • Demonstrated that Peg3-DMR genetic manipulation, not other locus changes, drives these effects.
    • Highlighted the unidirectional nature of this regulatory mechanism.