Genome-Wide Analysis of Heteroduplex DNA in Mismatch Repair–Deficient Yeast Cells Reveals Novel Properties of Meiotic Recombination Pathways
2011

Genome-Wide Analysis of Meiotic Recombination in Yeast

Sample size: 7 publication 10 minutes Evidence: high

Author Information

Author(s): Emmanuelle Martini, Valérie Borde, Matthieu Legendre, Stéphane Audic, Béatrice Regnault, Guillaume Soubigou, Bernard Dujon, Bertrand Llorente

Primary Institution: CEA DSV/IRCM, Centre National de la Recherche Scientifique, France

Hypothesis

What are the mechanisms of meiotic double-strand break repair and the regulation of crossover formation?

Conclusion

The study reveals that meiotic recombination is more complex than previously thought, with multiple pathways contributing to crossover and non-crossover formation.

Supporting Evidence

  • The study identified 73 and 92 crossovers per meiosis on average in the presence and absence of Msh2, respectively.
  • COs and NCOs were identified after analysis of the segregation patterns of all natural polymorphic sites in the meiotic progeny.
  • MMR reduces COs genome-wide in a SK1 × S288C polymorphic hybrid, suggesting an increase of DSB repair using the sister chromatid.
  • The study provides a genome-wide view of hDNAs associated with COs and NCOs.
  • Complex strand transfer patterns were observed, indicating multiple pathways of recombination.
  • Significant differences in the number of NCOs were found between the presence and absence of Msh2.
  • Analysis revealed that a significant fraction of NCOs do not arise from simple SDSA, raising the idea that dHJs are also involved during NCO formation.
  • The findings suggest that meiotic recombination is well conserved through evolution.

Takeaway

When yeast cells make babies, they mix their DNA, but sometimes they do it in unexpected ways that can change how their genes are passed on.

Methodology

The study used a genome-wide analysis of strand-transfer intermediates in a yeast hybrid lacking the mismatch repair protein Msh2.

Potential Biases

Potential bias due to the specific genetic backgrounds of the yeast strains used in the study.

Limitations

The study may not fully represent all recombination events due to the specific yeast strains used.

Participant Demographics

The study involved yeast cells, specifically a hybrid of SK1 and S288C strains.

Statistical Information

P-Value

0.021

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pgen.1002305

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