4.8 Article

Meiotic sister chromatid exchanges are rare in C. elegans

Journal

CURRENT BIOLOGY
Volume 31, Issue 7, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2020.11.018

Keywords

-

Funding

  1. NIH Office of Research Infrastructure Programs [P40 OD010440]
  2. Genetics Training Grant [5T32GM007464]
  3. NIGMS [1R35GM128804]
  4. University of Utah
  5. Pilot Project Award from the American Cancer Society

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The study found that sister chromatid exchanges (SCEs) are rare in meiosis in C. elegans germline, with crossover pathways used only to generate a necessary link between homologous chromosomes. Noncrossover pathways, on the other hand, repair almost all other double-strand breaks in this organism.
Sexual reproduction shuffles the parental genomes to generate new genetic combinations. To achieve that, the genome is subjected to numerous double-strand breaks, the repair of which involves two crucial decisions: repair pathway and repair template.(1) Use of crossover pathways with the homologous chromosome as template exchanges genetic information and directs chromosome segregation. Crossover repair, however, can compromise the integrity of the repair template and is therefore tightly regulated. The extent to which crossover pathways are used during sister-directed repair is unclear because the identical sister chromatids are difficult to distinguish. Nonetheless, indirect assays have led to the suggestion that inter-sister crossovers, or sister chromatid exchanges (SCEs), are quite common.(2-11) Here we devised a technique to directly score physiological SCEs in the C. elegans germline using selective sister chromatid labeling with the thymidine analog 5-ethynyl-2'-deoxyuridine (EdU). Surprisingly, we find SCEs to be rare in meiosis, accounting for <2% of repair events. SCEs remain rare even when the homologous chromosome is unavailable, indicating that almost all sister-directed repair is channeled into noncrossover pathways. We identify two mechanisms that limit SCEs. First, SCEs are elevated in the absence of the RecQ helicase BLMHIM-6. Second, the synaptonemal complex-a conserved interface that promotes crossover repair(12,13) -promotes SCEs when localized between the sisters. Our data suggest that crossover pathways in C. elegans are only used to generate the single necessary link between the homologous chromosomes. Noncrossover pathways repair almost all other breaks, regardless of the repair template.

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