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大鼠精子β-D-半乳糖苷酶的生物合成、加工及亚细胞定位

Biosynthesis, processing, and subcellular localization of rat spermbeta-D-galactosidase.

作者信息

Chayko C A, Orgebin-Crist M C, Skudlarek M D, Tulsiani D R

机构信息

Center for Reproductive Biology Research, Department of Obstetrics & Gynecology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2633, USA.

出版信息

Biol Reprod. 2000 Sep;63(3):688-96. doi: 10.1095/biolreprod63.3.688.

Abstract

During spermatogenesis, spermatids synthesize constituent proteins present in mature spermatozoa; however, little information exists on the molecular processes involved. In previous studies, this laboratory reported the characterization of rat sperm beta-D-galactosidase. In this paper, we report the localization of this enzyme along with its biosynthesis and processing. An antibody against rat luminal fluid beta-D-galactosidase was used to immunolocalize the enzyme in the testis and in epididymal spermatozoa. We found that beta-D-galactosidase is localized within the acrosomal cap of spermatids and in the acrosome and cytoplasmic droplet of epididymal spermatozoa. A combination of germ cell radiolabeling, immunoprecipitation, SDS-PAGE, and autoradiography revealed that spermatids produce two forms of beta-D-galactosidase, 90 and 88 kDa. During pulse-chase analysis, a 56-kDa form appeared. Treatment of beta-D-galactosidase immunoprecipitates from testicular spermatozoa with N-glycanase or Endo H revealed that both the 90- and 88-kDa forms become a 70-kDa polypeptide on SDS-PAGE. Since Endo H or N-glycanase treatment provided similar results, the presence of extensive N-linked high mannose/hybrid-type glycans on these proteins is indicated. Treatment of the 56-kDa form of beta-D-galactosidase with Endo H or N-glycanase resulted in the appearance of 52- and 50-kDa forms, respectively. This result suggests that the 56-kDa form contains N-linked high mannose/hybrid as well as complex oligosaccharides. During epididymal maturation, the 90-kDa form of beta-D-galactosidase persists in caput epididymal spermatozoa and is gradually converted to a major 74-kDa form in cauda spermatozoa. In addition to the 90- to 74-kDa forms, cauda spermatozoa show a 56- to 52-kDa form on Western immunoblots. Since only the high-molecular weight forms of beta-D-galactosidase are present on immunoblots of isolated sperm heads, we suggest that they are acrosomal in origin and that the 56-kDa form, which is processed to 52 kDa in cauda spermatozoa, is associated with the cytoplasmic droplet.

摘要

在精子发生过程中,精子细胞合成成熟精子中存在的组成蛋白;然而,关于其中涉及的分子过程的信息却很少。在先前的研究中,本实验室报道了大鼠精子β-D-半乳糖苷酶的特性。在本文中,我们报道了这种酶的定位及其生物合成和加工过程。使用针对大鼠管腔液β-D-半乳糖苷酶的抗体对该酶在睾丸和附睾精子中进行免疫定位。我们发现β-D-半乳糖苷酶定位于精子细胞的顶体帽内以及附睾精子的顶体和细胞质滴中。生殖细胞放射性标记、免疫沉淀、SDS-PAGE和放射自显影相结合的方法表明,精子细胞产生两种形式的β-D-半乳糖苷酶,分子量分别为90 kDa和88 kDa。在脉冲追踪分析过程中,出现了一种56 kDa的形式。用N-糖苷酶或内切糖苷酶H处理来自睾丸精子的β-D-半乳糖苷酶免疫沉淀物后,在SDS-PAGE上90 kDa和88 kDa的形式均变为70 kDa的多肽。由于内切糖苷酶H或N-糖苷酶处理得到了相似的结果,表明这些蛋白质上存在大量的N-连接高甘露糖/杂合型聚糖。用内切糖苷酶H或N-糖苷酶处理56 kDa形式的β-D-半乳糖苷酶后,分别出现了52 kDa和50 kDa的形式。这一结果表明56 kDa的形式既含有N-连接高甘露糖/杂合型聚糖,也含有复合寡糖。在附睾成熟过程中,90 kDa形式的β-D-半乳糖苷酶在附睾头精子中持续存在,并在附睾尾精子中逐渐转变为主要的74 kDa形式。除了90 kDa到74 kDa的形式外,附睾尾精子在Western免疫印迹上还显示出56 kDa到52 kDa的形式。由于在分离的精子头部的免疫印迹上仅存在高分子量形式的β-D-半乳糖苷酶,我们认为它们起源于顶体,而在附睾尾精子中加工为52 kDa的56 kDa形式与细胞质滴相关。

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