SCF <sup>RMF</sup> -dependent degradation of the nuclear lamina releases the somatic chromatin mobility restriction for meiotic recombination
Meiosis prepares the genome for sexual reproduction and is a driver of genetic diversity. Essential for both aspects are rapid chromosome movements enabling the pairing of homologous chromosomes, thereby promoting their recombination and ensuring their correct segregation afterward. However, it is unknown how meiocytes reorganize their nuclear architecture when chromosomes are tethered to the nuclear lamina in somatic cells. Here, we reveal the meiosis-specific Skp1-Cul1-F-box-protein (SCF) E3 ubiquitin ligase SCF<sup>RMF</sup> as a key regulator of this reorganization in <i>Arabidopsis</i>. We find that the nuclear lamina proteins of the CRWN family are degraded in an SCF<sup>RMF</sup>-dependent manner in this process. Thus, the SCF<sup>RMF</sup> functions to release the somatic constraints on chromosome mobility through disrupting the nuclear lamina, allowing homologous chromosomes to pair.
Authors
- Xinjie Yuan
- Bowei Cai (ORCID: https://orcid.org/0000-0002-9979-0828)
- Chao Yang (ORCID: https://orcid.org/0000-0002-4035-6453)
- Yuki Hamamura
- Arp Schnittger (ORCID: https://orcid.org/0000-0001-7067-0091)
Institutions
- Universität Hamburg (DE)
- Huazhong Agricultural University (CN)
- Max Planck Institute of Molecular Plant Physiology (DE)
Publication Details
- Journal
- Science Advances
- Published
- 2025-02-21
- DOI
- https://doi.org/10.1126/sciadv.adr4567
- Citations
- 5
- Primary Topic
- DNA Repair Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 4.03