Abstract
Meiosis produces four haploid cells after two successive divisions in sexually reproducing organisms. A critical event during meiosis is construction of the synaptonemal complex (SC), a large, protein-based bridge that physically links homologous chromosomes. The SC facilitates meiotic recombination, chromosome compaction, and the eventual separation of homologous chromosomes at metaphase I. We present experiments directly measuring physical properties of captured mammalian meiotic prophase I chromosomes. Mouse meiotic chromosomes are about ten-fold stiffer than somatic mitotic chromosomes, even for genetic mutants lacking SYCP1, the central element of the SC. Meiotic chromosomes dissolve when treated with nucleases, but only weaken when treated with proteases, suggesting that the SC is not rigidly connected, and that meiotic prophase I chromosomes are a gel meshwork of chromatin, similar to mitotic chromosomes. These results are consistent with a liquid- or liquid-crystal SC, but with SC-chromatin stiff enough to mechanically drive crossover interference.
Original language | English (US) |
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Article number | 542 |
Journal | Communications Biology |
Volume | 3 |
Issue number | 1 |
DOIs | |
State | Published - Dec 1 2020 |
Funding
We thank Supipi Mirihagalle, Lois Suh, and Tianming You for help with mouse husbandry and data collection. Work at NU was supported by NIH grants R01-GM105847, U54-CA193419 (CR-PS-OC) and a subcontract to grant U54-DK107980 (4D Nucleome). Work at University of Illinois, Urbana-Champaign was supported by NIH grants R00-HD082375 and R01-GM135549.
ASJC Scopus subject areas
- Medicine (miscellaneous)
- General Biochemistry, Genetics and Molecular Biology
- General Agricultural and Biological Sciences