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小鼠透明带基因与糖蛋白。

Mouse zona pellucida genes and glycoproteins.

作者信息

Wassarman P M, Jovine L, Litscher E S

机构信息

Brookdale Department of Molecular, Cell and Developmental Biology, Mount Sinai School of Medicine, New York, NY 10029-6574, USA.

出版信息

Cytogenet Genome Res. 2004;105(2-4):228-34. doi: 10.1159/000078193.

Abstract

The zona pellucida (ZP) is a thick extracellular coat that surrounds all mammalian eggs. The ZP plays important roles during oogenesis, fertilization, and preimplantation development. The mouse ZP consists of only three glycoproteins, called ZP1, ZP2, and ZP3. All three glycoproteins are essential structural components of the ZP. Additionally, ZP3 serves as a primary sperm receptor and acrosome reaction-inducer, and ZP2 serves as a secondary sperm receptor during fertilization. ZP1, ZP2, and ZP3 are encoded by single-copy genes present on three different chromosomes. The genes are expressed exclusively by mouse oocytes as they grow and the cellular specificity can be ascribed to cis-acting sequences close to the site of transcription initiation and to certain trans-acting factors. Concomitantly, ZP polypeptides are synthesized, modified with N- and O-linked oligosaccharides, secreted, and assembled into crosslinked filaments that exhibit a structural repeat. Nascent ZP glycoproteins are incorporated into large secretory vesicles that fuse with the oocyte plasma membrane and deposit nascent ZP glycoproteins into the innermost layer of the thickening ZP. Each ZP polypeptide possesses several characteristic features, including an N-terminal signal sequence, a ZP domain, a consensus furin cleavage site, and a C-terminal transmembrane domain. The latter is required for assembly of nascent ZP polypeptides into a ZP, cleavage at the consensus furin cleavage site is required for secretion, and the ZP domain supports protein:protein interactions during ZP assembly. At ovulation, when meiotic maturation of oocytes occurs and chromosomes condense into bivalents, expression of the three ZP genes ceases. Using "knockout mice", in the absence of either ZP2 or ZP3 expression, a ZP fails to assemble around growing oocytes and females are infertile. There is no effect on males. In the absence of ZP1 expression, a disorganized ZP assembles around growing oocytes and females exhibit reduced fertility. These observations are consistent with the current model for ZP structure in which ZP2 and ZP3 form long Z filaments crosslinked by ZP1.

摘要

透明带(ZP)是一层厚厚的细胞外被膜,包裹着所有哺乳动物的卵子。透明带在卵子发生、受精和着床前发育过程中发挥着重要作用。小鼠的透明带仅由三种糖蛋白组成,分别称为ZP1、ZP2和ZP3。这三种糖蛋白都是透明带的重要结构成分。此外,ZP3作为主要的精子受体和顶体反应诱导剂,而ZP2在受精过程中作为次要的精子受体。ZP1、ZP2和ZP3由位于三条不同染色体上的单拷贝基因编码。这些基因仅在小鼠卵母细胞生长时由其表达,细胞特异性可归因于靠近转录起始位点的顺式作用序列和某些反式作用因子。与此同时,ZP多肽被合成,经N-和O-连接寡糖修饰,分泌并组装成具有结构重复的交联细丝。新生的ZP糖蛋白被整合到大型分泌小泡中,这些小泡与卵母细胞质膜融合,并将新生的ZP糖蛋白沉积到增厚的透明带的最内层。每个ZP多肽都具有几个特征,包括N端信号序列、ZP结构域、共有弗林蛋白酶切割位点和C端跨膜结构域。后者是新生ZP多肽组装成透明带所必需的,在共有弗林蛋白酶切割位点的切割是分泌所必需的,而ZP结构域在透明带组装过程中支持蛋白质与蛋白质的相互作用。在排卵时,当卵母细胞发生减数分裂成熟且染色体浓缩成双价体时,三种ZP基因的表达停止。使用“基因敲除小鼠”,在缺乏ZP2或ZP3表达的情况下,透明带无法在生长中的卵母细胞周围组装,雌性小鼠不育。对雄性小鼠没有影响。在缺乏ZP1表达的情况下,无序的透明带在生长中的卵母细胞周围组装,雌性小鼠的生育能力降低。这些观察结果与目前的透明带结构模型一致,即ZP2和ZP3形成由ZP1交联的长Z细丝。

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