Murakami Eri, Shionoya Takao, Komenoi Suguru, Suzuki Yuji, Sakane Fumio
Department of Chemistry, Graduate School of Science, Chiba University, Chiba, Japan.
PLoS One. 2016 Sep 19;11(9):e0162997. doi: 10.1371/journal.pone.0162997. eCollection 2016.
Diacylglycerol kinase (DGK) phosphorylates DG to generate phosphatidic acid. Recently, we found that a new alternative splicing product of the DGKη gene, DGKη3, which lacks exon 26 encoding 31 amino acid residues, was expressed only in the secondary spermatocytes and round spermatids of the testis. In this study, we cloned the full length DGKη3 gene and confirmed the endogenous expression of its protein product. During the cloning procedure, we found a new testis-specific alternative splicing product of the DGKη gene, DGKη4, which lacks half of the catalytic domain. We examined the DGK activity and subcellular localization of DGKη3 and η4. DGKη3 had almost the same activity as DGKη1, whereas the activity of DGKη4 was not detectable. In resting NEC8 cells (human testicular germ cell tumor cell line), DGKη1, η3 and η4 were broadly distributed in the cytoplasm. When osmotically shocked, DGKη1 and η4 were distributed in punctate vesicles in the cytoplasm. In contrast, DGKη3 was partly translocated to the plasma membrane and co-localized with the actin cytoskeleton. These results suggest that DGKη3 and η4 have properties different from those of DGKη1 and that they play roles in the testis in a different manner.
二酰基甘油激酶(DGK)使二酰基甘油(DG)磷酸化以生成磷脂酸。最近,我们发现DGKη基因的一种新的可变剪接产物DGKη3,它缺少编码31个氨基酸残基的第26外显子,仅在睾丸的次级精母细胞和圆形精子细胞中表达。在本研究中,我们克隆了全长DGKη3基因并证实了其蛋白产物的内源性表达。在克隆过程中,我们发现了DGKη基因的一种新的睾丸特异性可变剪接产物DGKη4,它缺少一半的催化结构域。我们检测了DGKη3和η4的DGK活性及亚细胞定位。DGKη3的活性与DGKη1几乎相同,而DGKη4的活性无法检测到。在静息的NEC8细胞(人睾丸生殖细胞肿瘤细胞系)中,DGKη1、η3和η4广泛分布于细胞质中。当受到渗透压冲击时,DGKη1和η4分布于细胞质中的点状囊泡中。相比之下,DGKη3部分转位至质膜并与肌动蛋白细胞骨架共定位。这些结果表明,DGKη3和η4具有与DGKη1不同的特性,并且它们在睾丸中以不同方式发挥作用。