FBXO47 is essential for preventing the synaptonemal complex from premature disassembly in mouse male meiosis

• Published in: iScience 2022-04, Vol.25 (4), p.104008-104008, Article 104008
• Main Authors: Tanno, Nobuhiro, Takemoto, Kazumasa, Takada-Horisawa, Yuki, Shimada, Ryuki, Fujimura, Sayoko, Tani, Naoki, Takeda, Naoki, Araki, Kimi, Ishiguro, Kei-ichiro
• Format: Article
• Language: English
• Subjects: Biological sciences; Cell biology; Molecular biology
• ISSN: 2589-0042; 2589-0042
• DOI: 10.1016/j.isci.2022.104008

Meiotic prophase I is a prolonged G2 phase that ensures the completion of numerous meiosis-specific chromosome events. During meiotic prophase I, homologous chromosomes undergo synapsis to facilitate meiotic recombination yielding crossovers. It remains largely elusive how homolog synapsis is temporally maintained and destabilized during meiotic prophase I. Here we show that FBXO47 is the stabilizer of the synaptonemal complex during male meiotic prophase I. Disruption of FBXO47 shows severe impact on homologous chromosome synapsis, meiotic recombination, and XY body formation, leading to male infertility. Notably, in the absence of FBXO47, although once homologous chromosomes are synapsed, the synaptonemal complex is precociously disassembled before progressing beyond pachytene. Remarkably, Fbxo47 KO spermatocytes remain in an earlier stage of meiotic prophase I and lack crossovers, despite apparently exhibiting diplotene-like chromosome morphology. We propose that FBXO47 plays a crucial role in preventing the synaptonemal complex from premature disassembly during cell cycle progression of meiotic prophase I. [Display omitted] •FBXO47 is a stabilizer of the synaptonemal complex during male meiotic prophase•FBXO47 KO shows precocious disassembly of the synaptonemal complex•FBXO47 may function independently of SCF E3 ligase to maintain homolog synapsis Biological sciences; Molecular biology; Cell biology