Department of Reproductive Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, 157-8535, Japan.
Department of Reproductive Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, 157-8535, Japan; Department of Perinatal Medicine and Maternal Care, National Center for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, 157-8535, Japan.
Reprod Toxicol. 2018 Mar;76:71-77. doi: 10.1016/j.reprotox.2018.01.001. Epub 2018 Feb 3.
The ubiquitin-proteasome system, which is initiated by a single ubiquitin-activating enzyme E1 (UBE1), is involved in male reproduction via spermatogenesis and function in mammals. Here we explored the influence of UBE1-specific inhibitor, 4[4-(5-nitro-furan-2-ylmethylene)-3,5-dioxo-pyrazolidin-1-yl]-benzoic acid ethyl ester (pyrazone-41 or PYR-41) in female reproduction. UBE-1 was detected by immunoblotting and immunocytochemistry in mouse eggs and was localized mainly under the egg plasma membrane. PYR-41 pretreatment suppresses the development of eggs into two-cell embryos. Specifically, pretreatment retarded sperm enlargement and meiotic chromosomal division after sperm-egg fusion. PYR-41 pretreatment disturbed β-catenin, a well-known target protein for ubiquitination, localization under the egg plasma membrane and on spindle microtubules in wild-type eggs. Otherwise, PYR-41 treatment had no effect on the two-cell development of eggs lacking β-catenin. Our results raise the possibility that inhibition of the ubiquitin-proteasome system suppresses sperm enlargement through impaired β-catenin-mediated mechanism.
泛素-蛋白酶体系统由单一的泛素激活酶 E1(UBE1)启动,通过精子发生参与哺乳动物的雄性生殖,并在其功能中发挥作用。在这里,我们探索了泛素 E1 特异性抑制剂,4[4-(5-硝基-呋喃-2-基亚甲基)-3,5-二氧代-吡唑烷-1-基]-苯甲酸乙酯(吡唑酮 41 或 PYR-41)对雌性生殖的影响。UBE-1 通过免疫印迹和免疫细胞化学在小鼠卵中被检测到,主要定位于卵质膜下。PYR-41 预处理抑制卵发育成二细胞胚胎。具体而言,预处理延迟了精子-卵融合后精子的扩大和减数分裂染色体分裂。PYR-41 预处理扰乱了β-连环蛋白(一种已知的泛素化靶蛋白)在野生型卵质膜下和纺锤体微管上的定位。另一方面,PYR-41 处理对缺乏β-连环蛋白的卵的二细胞发育没有影响。我们的结果提出了这样一种可能性,即抑制泛素-蛋白酶体系统通过受损的β-连环蛋白介导的机制抑制精子扩大。