Puglisi Rossella, Tramer Federica, Panfili Enrico, Micali Fulvio, Sandri Gabriella, Boitani Carla
Department of Histology and Medical Embryology, University of Rome "La Sapienza," 00161 Rome, Italy.
Biol Reprod. 2003 Feb;68(2):405-11. doi: 10.1095/biolreprod.102.006544.
Phospholipid hydroperoxide glutathione peroxidase (PHGPx, 20 kDa) and sperm nuclei glutathione peroxidase (snGPx, 34 kDa) are two selenoproteins present in mammalian testis and epididymal spermatozoa. They originate from the differential splicing of the PHGPx gene and appear to play important roles in sperm physiology. To determine the stages of spermatogenesis in which they are present, we compared the expression pattern of these two enzymes in highly purified populations of germ cells during specific phases of differentiation. In Northern and Western blotting experiments, both PHGPx transcript and protein were markedly expressed in pachytene spermatocytes and round spermatids. In contrast, the testis-specific snGPx was detected at both the mRNA and protein level only in haploid round spermatids. Accordingly, the developmental analysis of testicular RNAs from rats of different ages first revealed the appearance of PHGPx and snGPx transcripts at Day 20 and Day 30, respectively. Furthermore, both meiotic and postmeiotic cells contained catalytically active PHGPx/snGPx, with higher activity in the haploid cells. The intracellular distribution of PHGPx in mitochondria and nuclei of meiotic cells was demonstrated by immunocytochemical electron microscopy and Western blotting. These findings provide evidence that the PHGPx gene is differentially spliced during the meiotic prophase and haploid cell phases of spermatogenesis.
磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPx,20 kDa)和精子核谷胱甘肽过氧化物酶(snGPx,34 kDa)是存在于哺乳动物睾丸和附睾精子中的两种硒蛋白。它们源自PHGPx基因的可变剪接,似乎在精子生理过程中发挥重要作用。为了确定它们存在于精子发生的哪些阶段,我们比较了这两种酶在分化特定阶段高度纯化的生殖细胞群体中的表达模式。在Northern印迹和Western印迹实验中,PHGPx转录本和蛋白在粗线期精母细胞和圆形精子细胞中均有明显表达。相比之下,睾丸特异性snGPx仅在单倍体圆形精子细胞的mRNA和蛋白水平上被检测到。因此,对不同年龄大鼠睾丸RNA的发育分析首先分别在第20天和第30天发现了PHGPx和snGPx转录本的出现。此外,减数分裂细胞和减数分裂后细胞均含有具有催化活性的PHGPx/snGPx,在单倍体细胞中活性更高。通过免疫细胞化学电子显微镜和Western印迹证实了PHGPx在减数分裂细胞的线粒体和细胞核中的细胞内分布。这些发现提供了证据,表明PHGPx基因在精子发生的减数分裂前期和单倍体细胞期发生了可变剪接。