TY - JOUR
T1 - Micromanipulation of prophase I chromosomes from mouse spermatocytes reveals high stiffness and gel-like chromatin organization
AU - Biggs, Ronald J
AU - Liu, Ning
AU - Peng, Yiheng
AU - Marko, John F
AU - Qiao, Huanyu
N1 - Funding Information:
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.
PY - 2020/12/1
Y1 - 2020/12/1
N2 - 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.
AB - 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.
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U2 - 10.1038/s42003-020-01265-w
DO - 10.1038/s42003-020-01265-w
M3 - Article
C2 - 32999386
SN - 2399-3642
VL - 3
SP - 542
JO - Communications biology
JF - Communications biology
IS - 1
M1 - 542
ER -