Evans J P, Schultz R M, Kopf G S
Department of Obstetrics and Gynecology, School of Medicine, University of Pennsylvania, Philadelphia 19104, USA.
J Cell Sci. 1995 Oct;108 ( Pt 10):3267-78. doi: 10.1242/jcs.108.10.3267.
The guinea pig sperm protein, PH-30 (also known as fertilin), is postulated to participate in the interaction between the sperm and egg plasma membranes. The beta subunit of guinea pig PH-30 (gpPH-30 beta) contains a domain with homology to disintegrins, snake venom proteins that bind to integrins via an integrin-binding domain containing the tripeptide RGD. This raises the question of whether an egg integrin serves as a receptor for PH-30. Although mouse eggs express integrin subunits, their role in mouse fertilization is unresolved. Therefore, we examined fertilization for two different hallmarks of integrin function, namely, dependence of ligand binding on divalent cations and the ability to inhibit ligand binding with RGD peptides. We demonstrate that sperm binding to zona pellucida-free eggs is supported by Ca2+, Mg2+, or Mn2+. Ca2+ was necessary and sufficient for sperm-egg fusion, with 2.5 mM Ca2+ being the most effective concentration. In addition, fertilization could be partially inhibited with various RGD peptides, which caused a decrease in sperm-egg fusion by 30-58%. This partial inhibition of fusion with RGD peptides prompted the cloning of the mouse homologue of gpPH-30 beta (hereafter referred to as mPH-30 beta) to determine if it possessed the tripeptide RGD or a different amino acid sequence in its disintegrin domain. mPH-30 beta, which is expressed during meiotic and post-meiotic phases of spermatogenesis, shares significant similarities to gpPH-30 beta throughout the length of the molecule, from the signal sequence to the cytoplasmic tail. The full-length deduced amino acid sequence of mPH-30 beta. The disintegrin domain of mPH-30 beta has the tripeptide QDE (instead of RGD) in its cell recognition region. Peptides containing this QDE sequence decrease the binding and fusion of sperm with zona pellucida-free eggs by approximately 70%, suggesting that the disintegrin domain of mPH-30 beta participates in the interaction between sperm and egg membranes.
豚鼠精子蛋白PH - 30(也称为受精素)被推测参与精子与卵质膜之间的相互作用。豚鼠PH - 30(gpPH - 30β)的β亚基包含一个与解整合素具有同源性的结构域,解整合素是一种蛇毒蛋白,通过含有三肽RGD的整合素结合结构域与整合素结合。这就提出了一个问题,即卵整合素是否作为PH - 30的受体。尽管小鼠卵表达整合素亚基,但其在小鼠受精中的作用尚未明确。因此,我们研究了整合素功能的两个不同标志的受精情况,即配体结合对二价阳离子的依赖性以及用RGD肽抑制配体结合的能力。我们证明精子与无透明带卵的结合受到Ca2 +、Mg2 +或Mn2 +的支持。Ca2 +对于精卵融合是必需且充分的,2.5 mM Ca2 +是最有效的浓度。此外,各种RGD肽可部分抑制受精,这导致精卵融合减少30 - 58%。这种用RGD肽对融合的部分抑制促使克隆gpPH - 30β的小鼠同源物(以下称为mPH - 30β),以确定其在解整合素结构域中是否具有三肽RGD或不同的氨基酸序列。mPH - 30β在精子发生的减数分裂和减数分裂后阶段表达,从信号序列到细胞质尾,在整个分子长度上与gpPH - 30β具有显著相似性。mPH - 30β的全长推导氨基酸序列。mPH - 30β的解整合素结构域在其细胞识别区域具有三肽QDE(而非RGD)。含有该QDE序列的肽使精子与无透明带卵的结合和融合减少约70%,表明mPH - 30β的解整合素结构域参与精子与卵膜之间的相互作用。