Yi Young-Joo, Manandhar Gaurishankar, Sutovsky Miriam, Li Rongfeng, Jonáková Vera, Oko Richard, Park Chang-Sik, Prather Randall S, Sutovsky Peter
Department of Anatomy, University of Missouri-Columbia, Missouri 65211, USA.
Biol Reprod. 2007 Nov;77(5):780-93. doi: 10.1095/biolreprod.107.061275. Epub 2007 Aug 1.
The 26S proteasome, which is a multi-subunit protease with specificity for substrate proteins that are postranslationally modified by ubiquitination, has been implicated in acrosomal function and sperm-zona pellucida (ZP) penetration during mammalian fertilization. Ubiquitin C-terminal hydrolases (UCHs) are responsible for the removal of polyubiquitin chains during substrate priming for proteasomal proteolysis. The inhibition of deubiquitination increases the rate of proteasomal proteolysis. Consequently, we have hypothesized that inhibition of sperm acrosome-borne UCHs increases the rate of sperm-ZP penetration and polyspermy during porcine in vitro fertilization (IVF). Ubiquitin aldehyde (UA), which is a specific nonpermeating UCH inhibitor, significantly (P < 0.05) increased polyspermy during porcine IVF and reduced (P < 0.05) UCH enzymatic activity measured in motile boar spermatozoa using a specific fluorometric UCH substrate, ubiquitin-AMC. Antibodies against two closely related UCHs, UCHL1 and UCHL3, detected these UCHs in the oocyte cortex and on the sperm acrosome, respectively, and increased the rate of polyspermy during IVF, consistent with the UA-induced polyspermy surge. In the oocyte, UCHL3 was primarily associated with the meiotic spindle. Sperm-borne UCHL3 was localized to the acrosomal surface and coimmunoprecipitated with a peripheral acrosomal membrane protein, spermadhesin AQN1. Recombinant UCHs, UCHL3, and isopeptidase T reduced polyspermy when added to the fertilization medium. UCHL1 was detected in the oocyte cortex but not on the sperm surface, and was partially degraded 6-8 h after fertilization. Enucleated oocyte-somatic cell electrofusion caused polarized redistribution of cortical UCHL1. We conclude that sperm-acrosomal UCHs are involved in sperm-ZP interactions and antipolyspermy defense. Modulation of UCH activity could facilitate the management of polyspermy during IVF and provide insights into male infertility.
26S蛋白酶体是一种多亚基蛋白酶,对经泛素化进行翻译后修饰的底物蛋白具有特异性,在哺乳动物受精过程中与顶体功能及精子穿透透明带(ZP)有关。泛素C末端水解酶(UCHs)负责在蛋白酶体蛋白水解的底物引发过程中去除多聚泛素链。去泛素化的抑制会增加蛋白酶体蛋白水解的速率。因此,我们推测抑制精子顶体携带的UCHs可提高猪体外受精(IVF)过程中精子穿透ZP和多精受精的速率。泛素醛(UA)是一种特异性非渗透性UCH抑制剂,在猪IVF过程中显著(P<0.05)增加了多精受精,并使用特异性荧光UCH底物泛素-AMC降低了(P<0.05)在活动公猪精子中测得的UCH酶活性。针对两种密切相关的UCHs,即UCHL1和UCHL3的抗体,分别在卵母细胞皮质和精子顶体上检测到了这些UCHs,并在IVF过程中增加了多精受精的速率,这与UA诱导的多精受精激增一致。在卵母细胞中,UCHL3主要与减数分裂纺锤体相关。精子携带的UCHL3定位于顶体表面,并与一种顶体外周膜蛋白精子黏附素AQN1共免疫沉淀。当添加到受精培养基中时,重组UCHs、UCHL3和异肽酶T可减少多精受精。UCHL1在卵母细胞皮质中被检测到,但不在精子表面,并且在受精后6-8小时部分降解。去核卵母细胞-体细胞电融合导致皮质UCHL1的极化重新分布。我们得出结论,精子顶体UCHs参与精子与ZP的相互作用和抗多精受精防御。UCH活性的调节可有助于在IVF过程中管理多精受精,并为男性不育症提供见解。