Department of Bioscience, Graduate School of Science and Technology, National University Corporation, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan.
Biological Science Course, Graduate School of Science, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan.
Gen Comp Endocrinol. 2024 Apr 1;349:114453. doi: 10.1016/j.ygcen.2024.114453. Epub 2024 Jan 27.
The prss59.1 gene was identified as one of 11 genes that were highly upregulated during the induction of ovulation in zebrafish by using an in vivo ovulation assay. Previously, we conducted biochemical characterization of Prss59.1 and revealed it to be a trypsin-like proteolytic enzyme. In this study, we established a prss59.1 gene knockout strain using the CRISPR/Cas9 system. Phenotypic analysis of prss59.1 knockout fish showed that prss59.1 is associated with chorion elevation, a prominent event in egg activation during fertilization. The chorions of heterozygous and homozygous prss59.1 mutant zebrafish were smaller than those of the wild type. The results suggested that Prss59.1 is necessary for chorion expansion. The homozygous prss59.1 mutant strain, with a small chorion, showed an extremely low survival rate. Fiber-supported knob-like structures (KS) on the chorion showed an abnormal structure in prss59.1 mutants. Prss59.1 was detected in the KS on the chorion. The pores on the chorion were smaller in the prss59.1 mutants than in the wild type. Transmission electron microscopy (TEM) observations of the cross sections of the chorions showed abnormalities in the chorion structure in prss59.1 mutants. These results demonstrated that Prss59.1 is involved in chorion elevation and in proper formation of the chorion, which is necessary for embryo development.
使用体内排卵测定法,我们鉴定了 prss59.1 基因,它是在斑马鱼排卵诱导过程中高度上调的 11 个基因之一。此前,我们对 Prss59.1 进行了生化特性分析,揭示它是一种胰蛋白酶样蛋白水解酶。在本研究中,我们使用 CRISPR/Cas9 系统建立了 prss59.1 基因敲除品系。prss59.1 敲除鱼的表型分析表明,prss59.1 与卵母细胞激活过程中的卵壳隆起有关,这是卵受精过程中的一个显著事件。杂合和纯合 prss59.1 突变型斑马鱼的卵壳比野生型小。结果表明 Prss59.1 对于卵壳扩张是必需的。具有小卵壳的纯合 prss59.1 突变体品系的存活率极低。卵壳上纤维支撑的结节状结构 (KS) 在 prss59.1 突变体中表现出异常结构。Prss59.1 在卵壳 KS 上被检测到。prss59.1 突变体的卵壳孔比野生型小。卵壳横截面的透射电子显微镜 (TEM) 观察显示 prss59.1 突变体的卵壳结构异常。这些结果表明 Prss59.1 参与了卵壳隆起和卵壳的正常形成,这对于胚胎发育是必需的。