Suppr超能文献

哺乳动物配子结合的分子基础。

Molecular basis of mammalian gamete binding.

作者信息

Miller David J, Shi Xudong, Burkin Heather

机构信息

Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana 61801, USA.

出版信息

Recent Prog Horm Res. 2002;57:37-73. doi: 10.1210/rp.57.1.37.

Abstract

Despite the importance of fertilization for controlling human reproduction, regulating animal production, and promoting preservation of endangered species, the molecular basis underlying gamete binding and fertilization has been perplexing. More progress has been made in the mouse than in other mammals and, recently, targeted deletion of specific genes in the mouse has yielded intriguing results. This review will emphasize research performed by our laboratory and others done primarily with mouse gametes but will include some interesting observations from other mammals. Studies of murine fertilization indicate that oligosaccharides on the egg coat glycoprotein ZP3 bind sperm. The precise oligosaccharides that bind sperm are the subject of considerable debate. ZP3 also induces exocytosis of the sperm acrosome, allowing sperm to penetrate through the egg coat (zona pellucida). A number of candidate ZP3 receptors have been proposed and studies of beta1,4galactosyltransferase-I (GalT-I) are reviewed here in the most detail. Sperm from mice with a targeted deletion of GalT-I still are able to bind the zona pellucida but are unable to acrosome react and penetrate through the zona. Therefore, the unique role of GalT-I appears to be in signal transduction. GalT-I forms a complex with heterotrimeric G proteins and activates signaling, leading to exocytosis in sperm and in heterologous cells expressing GalT-I. Other signaling steps triggered by GalT-I are under active investigation; this receptor forms a complex with a protein kinase anchoring protein. After exocytosis of the acrosome, sperm penetrate the zona pellucida and fuse with the oocyte plasma membrane using ADAM family members on sperm and integrins on oocytes. These proteins, along with the tetraspanins on oocytes, may form a complex web at gamete fusion. Targeted deletion of specific genes in this putative complex has provided important information about their redundancy. After the oocyte is fertilized, the binding site for GalT-I is lost from ZP3, preventing additional sperm from binding to the zona pellucida. New technical advances and creative ideas offer the opportunity to make important advances and to solve the conundrum of fertilization.

摘要

尽管受精对于控制人类生殖、调节动物生产以及促进濒危物种的保护至关重要,但其配子结合和受精的分子基础一直令人困惑。在小鼠身上取得的进展比在其他哺乳动物身上更多,最近,在小鼠中对特定基因进行靶向缺失产生了有趣的结果。本综述将重点介绍我们实验室以及其他主要以小鼠配子进行的研究,但也会包括来自其他哺乳动物的一些有趣观察结果。对小鼠受精的研究表明,卵被糖蛋白ZP3上的寡糖与精子结合。与精子结合的精确寡糖是一个备受争议的话题。ZP3还诱导精子顶体的胞吐作用,使精子能够穿透卵被(透明带)。已经提出了许多候选的ZP3受体,这里将最详细地综述β1,4半乳糖基转移酶-I(GalT-I)的研究。来自GalT-I靶向缺失小鼠的精子仍然能够结合透明带,但无法发生顶体反应并穿透透明带。因此,GalT-I的独特作用似乎在于信号转导。GalT-I与异源三聚体G蛋白形成复合物并激活信号传导,导致精子和表达GalT-I的异源细胞中的胞吐作用。由GalT-I触发的其他信号传导步骤正在积极研究中;该受体与一种蛋白激酶锚定蛋白形成复合物。顶体胞吐后,精子穿透透明带并利用精子上的ADAM家族成员和卵母细胞上的整合素与卵母细胞质膜融合。这些蛋白质,连同卵母细胞上的四跨膜蛋白,可能在配子融合处形成一个复杂的网络。在这个假定的复合物中对特定基因进行靶向缺失提供了有关它们冗余性的重要信息。卵母细胞受精后,ZP3上GalT-I的结合位点丢失,阻止额外的精子与透明带结合。新的技术进步和创新想法为取得重要进展和解决受精难题提供了机会。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验