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Related Concept Videos

Crossing Over01:30

Crossing Over

Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to allelic diversity in the newly formed daughter cells. In humans, crossing over produces genetically distinct haploid egg and sperm cells that undergo fertilization to produce unique offspring. Before cell division starts, the germ cell’s chromosome(s) undergo duplication in the S phase of the cell cycle. As the cells enter prophase I, duplicated...
Gene Conversion02:08

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...
Gene Conversion02:08

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...
Pedigree Analysis01:35

Pedigree Analysis

Overview
Pedigree Analysis01:35

Pedigree Analysis

Overview
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...

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Related Experiment Video

Updated: May 29, 2026

Frequency and Distribution of Crossovers in Caenorhabditis elegans Meiosis by SNP Genotyping using Real-time PCR
06:18

Frequency and Distribution of Crossovers in Caenorhabditis elegans Meiosis by SNP Genotyping using Real-time PCR

Published on: July 11, 2025

Age-dependent recombination rates in human pedigrees.

Julie Hussin1, Marie-Hélène Roy-Gagnon, Roxanne Gendron

  • 1Department of Biochemistry, Faculty of Medicine, University of Montreal, Montreal, Canada.

Plos Genetics
|September 14, 2011
PubMed
Summary

Maternal age is linked to changes in human recombination. This study found that recombination rates significantly decrease with advancing maternal age, potentially increasing aneuploidy risk.

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Area of Science:

  • Human Genetics
  • Reproductive Biology
  • Genomic Instability

Background:

  • Chromosome-number abnormalities, such as trisomies, are associated with altered recombination and increased maternal age.
  • Understanding age-related effects on recombination is crucial for elucidating mechanisms behind human trisomies.

Purpose of the Study:

  • To investigate the relationship between maternal age and recombination rate in the human population.
  • To explore how age-related changes in recombination might contribute to aneuploidy.

Main Methods:

  • High-resolution localization of crossovers using over 600,000 genetic markers.
  • Genotyping of 69 French-Canadian pedigrees, analyzing recombination events in 195 maternal meioses.

Main Results:

  • Observed general patterns of fine-scale recombination rate variation consistent with previous studies.
  • First observation of a significant decrease in human recombination rates with advancing maternal age.
  • This decrease is likely chromosome-specific, affecting middle chromosomal arm sections and subtelomeric regions.

Conclusions:

  • Recombination rates decline with increasing maternal age, potentially impacting chromosome segregation.
  • Reduced recombination efficiency with maternal age may decrease protection against non-disjunction.
  • This finding offers a model to explain the association between maternal age and trisomy rates.