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Multivalent weak interactions between assembly units drive synaptonemal complex formation.

Zhenguo Zhang | Songbo Xie | Ruoxi Wang | Shuqun Guo | Qiuchen Zhao | Hui Nie | Yuanyuan Liu | Fengguo Zhang | Miao Chen | Libo Liu | Xiaoqian Meng | Min Liu | Li Zhao | Monica P Colaiácovo | Jun Zhou | Jinmin Gao
The Journal of cell biology | 2020

The synaptonemal complex (SC) is an ordered but highly dynamic structure assembled between homologous chromosomes to control interhomologous crossover formation, ensuring accurate meiotic chromosome segregation. However, the mechanisms regulating SC assembly and dynamics remain unclear. Here, we identified two new SC components, SYP-5 and SYP-6, in Caenorhabditis elegans that have distinct expression patterns and form distinct SC assembly units with other SYPs through stable interactions. SYP-5 and SYP-6 exhibit diverse in vivo SC regulatory functions and distinct phase separation properties in cells. Charge-interacting elements (CIEs) are enriched in SC intrinsically disordered regions (IDRs), and IDR deletion or CIE removal confirmed a requirement for these elements in SC regulation. Our data support the theory that multivalent weak interactions between the SC units drive SC formation and that CIEs confer multivalency to the assembly units.

Pubmed ID: 32211900

Research resources used in this publication

None found

Antibodies used in this publication

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Associated grants

  • Agency: NIH HHS, United States
    Id: P40 OD010440
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM072551

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PRISM (tool)

RRID:SCR_005375

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RRID:SCR_007341

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RRID:CVCL_0063

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