Graduate School of Environmental Science and Technology, Okayama University, Tsushimanaka, Kita, Okayama, Japan.
Faculty of Agriculture, Okayama University, Tsushimanaka, Kita, Okayama, Japan.
Reproduction. 2024 Aug 27;168(4). doi: 10.1530/REP-24-0030. Print 2024 Oct 1.
Repro57 mice, bearing an Rnf212 gene mutation, exhibit infertility in both homozygous mutant males and females, revealing arrested spermatogenesis in males and investigating unclear mechanisms in females. The study highlights aneuploidy and altered kinetochore patterns in repro57 homozygous mutant oocytes, which impact later stages of embryo development.
Repro57 mice, induced with N-ethyl-N-nitrosourea and harboring a mutation in the Rnf212 gene, exhibit infertility in both homozygous mutant males and females. Rnf212 plays a crucial role in recombination and crossover designation. In male repro57 homozygous mutants, spermatocytes often degenerate during late prophase, and mature spermatozoa are absent in the seminiferous epithelium, indicating arrested spermatogenesis as the cause of infertility. Despite reports of infertility in Rnf212-knockout female mice, the specific mechanisms underlying infertility in female repro57 homozygous mutants remain elusive. This study investigates the chromosomal and kinetochore patterns of mature oocytes and their developmental potential following in vitro fertilization in female repro57 homozygous mutant mice. While all wild-type oocytes progress to metaphase II and exhibit euploidy, all repro57 homozygous mutant mouse oocytes display aneuploidy. Additionally, kinetochore distances in repro57 homozygous mutant oocytes exceed those observed in wild-type counterparts. Although no significant differences are noted in fertilization and early embryo development rates between wild-type and repro57 homozygous mutant mice, embryos derived from repro57 homozygous mutants exhibit significantly lower morula and blastocyst rates, accompanied by frequent cytokinesis failure and vacuole formation. These findings suggest that the premature segregation of sister chromatids in repro57 homozygous mutant mice adversely impacts the later stages of embryo development.
简而言之,携带 Rnf212 基因突变的 Repro57 小鼠在纯合突变雄性和雌性中均表现出不育,雄性表现为精子发生停滞,雌性则表现出机制尚不清楚的不育。该研究强调了 Repro57 纯合突变卵母细胞中的非整倍体和动粒模式改变,这些改变会影响胚胎发育的后期阶段。
经 N-乙基-N-亚硝基脲诱导并携带 Rnf212 基因突变的 Repro57 小鼠在纯合突变雄性和雌性中均表现出不育。Rnf212 在重组和交叉指定中发挥关键作用。在雄性 Repro57 纯合突变体中,精母细胞在晚期前期经常退化,生精上皮中不存在成熟精子,表明精子发生停滞是不育的原因。尽管有报道称 Rnf212 敲除雌性小鼠不育,但雌性 Repro57 纯合突变体不育的具体机制仍不清楚。本研究调查了雌性 Repro57 纯合突变体小鼠成熟卵母细胞的染色体和动粒模式及其体外受精后的发育潜力。虽然所有野生型卵母细胞都进展到中期 II 并表现出整倍体,但所有 Repro57 纯合突变小鼠卵母细胞都显示出非整倍体。此外,Repro57 纯合突变卵母细胞中的动粒距离超过了野生型对照。尽管野生型和 Repro57 纯合突变小鼠的受精和早期胚胎发育率没有显著差异,但 Repro57 纯合突变体胚胎的桑葚胚和囊胚率明显较低,伴有频繁的胞质分裂失败和空泡形成。这些发现表明 Repro57 纯合突变小鼠中姐妹染色单体的过早分离对胚胎发育的后期阶段产生不利影响。