Issue 4, April 2026
During meiotic prophase I, programmed DNA double-strand breaks (DSBs) initiate homologous recombination to ensure accurate segregation of homologous chromosomes in oocytes. However, how these DSBs are formed and how their disruption compromises both oocyte quantity and quality remain elusive. In this issue, Wang et al. report the identification of mutations in MEI4, a key DSB gene, in patients with premature ovarian insufficiency. These mutations disrupt the assembly of the MEI4-containing DSB machinery on chromosome axes, impairing meiotic DSB formation and homologous chromosome synapsis, thereby leading to excessive oocyte loss and early embryonic arrest. The cover image uses a butterfly emerging from its chrysalis as a metaphor to illustrate the paradox that controlled chromosomal “fractures” are essential for recombination: golden chromosome-like fissures represent SPO11-dependent DSBs generated by the MEI4-containing machinery, from which a DNA-patterned butterfly rises, symbolizing successful synapsis, crossover formation, and the acquisition of oocyte developmental competence.
During meiotic prophase I, programmed DNA double-strand breaks (DSBs) initiate homologous recombination to ensure accurate segregation of homologous chromosomes in oocytes. However, how these DSBs are formed and how their disruption compromises both oocyte quantity and quality remain elusive. In this issue, Wang et al. report the identification of mutations in MEI4, a key DSB gene, in patients with premature ovarian insufficiency. These mutations disrupt the assembly of the MEI4-containing DSB machinery on chromosome axes, impairing meiotic DSB formation and homologous chromosome synapsis, thereby leading to excessive oocyte loss and early embryonic arrest. The cover image uses a butterfly emerging from its chrysalis as a metaphor to illustrate the paradox that controlled chromosomal “fractures” are essential for recombination: golden chromosome-like fissures represent SPO11-dependent DSBs generated by the MEI4-containing machinery, from which a DNA-patterned butterfly rises, symbolizing successful synapsis, crossover formation, and the acquisition of oocyte developmental competence.
Edited by Dr. Qing-Feng Wu, Dr. Wan-Jin Chen, Dr. Miao He, Dr. Chen Ming
Pages 1155-1304 (October 2025)
Edited by Prof. Xuehui Huang, Prof. Liangsheng Zhang, Prof. Shifeng Cheng, Associate Prof. Junpeng Shi, Prof. Fei He
Pages 719-868 (June 2025)
Edited by Prof. Shuhua Xu, Prof. Chuan-Chao Wang, Prof. Xin Jin, Prof. Hou-Feng Zheng, Prof. Li Jin
Pages 449-600 (April 2025)
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