4.6 Article

Oligopaint DNA FISH reveals telomere-based meiotic pairing dynamics in the silkworm, Bombyx mori

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PLOS GENETICS
卷 17, 期 7, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1009700

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资金

  1. Intramural Program of the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health (NIDDK) [DK015602]
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health (NICHD) [1K99HD104851]
  3. LabEx DEEP grants from the Agence National de la Recherche [ANR-11-LABX-0044, ANR-10-IDEX-0001-02]
  4. ATIP-AVENIR research grant from CNRS/INSERM
  5. European Research Council (ERC) [CENEVO-758757]
  6. Institut Curie
  7. Agence Nationale de la Recherche (ANR) [ANR-11-LABX-0044] Funding Source: Agence Nationale de la Recherche (ANR)

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Accurate chromosome segregation is crucial for reproductive success. The use of Oligopaints in the silkworm Bombyx mori has provided new insights into mechanisms of homolog pairing during meiosis, revealing asynchronous pairing, transcription-biased pairing in males, and similarities in bivalent formation with C. elegans. Furthermore, the study suggests that microtubule recruitment may be dependent on kinetochore proteins but independent of centromeres, and that telomeres play a central role in regulating chromosome interactions during sperm and egg development.
Accurate chromosome segregation during meiosis is essential for reproductive success. Yet, many fundamental aspects of meiosis remain unclear, including the mechanisms regulating homolog pairing across species. This gap is partially due to our inability to visualize individual chromosomes during meiosis. Here, we employ Oligopaint FISH to investigate homolog pairing and compaction of meiotic chromosomes and resurrect a classical model system, the silkworm Bombyx mori. Our Oligopaint design combines multiplexed barcoding with secondary oligo labeling for high flexibility and low cost. These studies illustrate that Oligopaints are highly specific in whole-mount gonads and on meiotic squashes. We show that meiotic pairing is robust in both males and females and that pairing can occur through numerous partially paired intermediate structures. We also show that pairing in male meiosis occurs asynchronously and seemingly in a transcription-biased manner. Further, we reveal that meiotic bivalent formation in B. mori males is highly similar to bivalent formation in C. elegans, with both of these pathways ultimately resulting in the pairing of chromosome ends with non-paired ends facing the spindle pole. Additionally, microtubule recruitment in both C. elegans and B. mori is likely dependent on kinetochore proteins but independent of the centromere-specifying histone CENP-A. Finally, using super-resolution microscopy in the female germline, we show that homologous chromosomes remain associated at telomere domains in the absence of chiasma and after breakdown and modification to the synaptonemal complex in pachytene. These studies reveal novel insights into mechanisms of meiotic homolog pairing both with or without recombination. Author summary Meiosis is the specialized cell division occurring exclusively in ovaries and testes to produce egg and sperm cells, respectively. The accurate distribution of chromosomes (the genetic material) during this process is essential to prevent infertility/sterility and developmental disorders in offspring. As researchers are specifically unable to study the mechanisms regulating meiosis in depth in humans, identifying broadly conserved aspects of meiotic chromosome segregation is essential for making accurate inferences about human biology. Here, we use a sophisticated chromosome painting approach called Oligopaints to visualize and study chromosomes during meiosis in the silkworm, Bombyx mori. Using this method, we show that chromosome ends (telomeres) play a central role in regulating interactions between maternal and paternal chromosome copies during both sperm and egg development.

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