Meiotic pairing through barcode-like satellite DNA repeats

Here, we use satellite DNA deletion, duplication, and translocation strains that are unique to Drosophila to demonstrate that repeat mismatches perturb meiotic pairing, particularly at centromeres and pericentromeres. Strains containing satellite DNA mismatches exhibit pairing defects that are likely driven by the incorrect association of similar repeats on non-homologous chromosomes. Notably, defective pairing also occurs in the progeny of D. melanogaster natural populations that have diverged in their satellite DNA content.

In the absence of homozygous satellite DNA arrays, we further show that pairing is antagonized by the HORMAD protein, Mad2, while a Pachytene checkpoint 2 (Pch2)-dependent meiotic delay can restore pairing. Finally, compromised meiotic pairing is strongly correlated with mid-oogenesis cell death, a quality control mechanism that likely culls defective oocytes to prevent chromosome mis-segregation and aneuploidy. Therefore, our findings resolve the debate on satellite DNA functionality by providing evidence for a role in meiotic pairing.

We propose that this repeat-based pairing mechanism exerts an underappreciated selective pressure, constraining the divergence of these rapidly evolving tandem repeats within interbreeding natural populations.