Biosynthesis, processing, and subcellular localization of rat sperm β-D-galactosidase

被引:7
作者
Chayko, CA
Orgebin-Crist, MC
Skudlarek, MD
Tulsiani, DRP
机构
[1] Vanderbilt Univ, Sch Med, Ctr Reprod Biol Res, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Obstet & Gynecol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Cell Biol, Nashville, TN 37232 USA
关键词
epididymis; sperm; sperm maturation; spermatid; spermatogenesis;
D O I
10.1095/biolreprod63.3.688
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页码:688 / 696
页数:9
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