Institute of Human Genetics, Georg-August-University of Göttingen, 37073 Göttingen, Germany.
Mol Biol Cell. 2011 May 15;22(10):1766-79. doi: 10.1091/mbc.E09-12-0993. Epub 2011 Apr 1.
Peroxisomal testis-specific 1 gene (Pxt1) is the only male germ cell-specific gene that encodes a peroxisomal protein known to date. To elucidate the role of Pxt1 in spermatogenesis, we generated transgenic mice expressing a c-MYC-PXT1 fusion protein under the control of the PGK2 promoter. Overexpression of Pxt1 resulted in induction of male germ cells' apoptosis mainly in primary spermatocytes, finally leading to male infertility. This prompted us to analyze the proapoptotic character of mouse PXT1, which harbors a BH3-like domain in the N-terminal part. In different cell lines, the overexpression of PXT1 also resulted in a dramatic increase of apoptosis, whereas the deletion of the BH3-like domain significantly reduced cell death events, thereby confirming that the domain is functional and essential for the proapoptotic activity of PXT1. Moreover, we demonstrated that PXT1 interacts with apoptosis regulator BAT3, which, if overexpressed, can protect cells from the PXT1-induced apoptosis. The PXT1-BAT3 association leads to PXT1 relocation from the cytoplasm to the nucleus. In summary, we demonstrated that PXT1 induces apoptosis via the BH3-like domain and that this process is inhibited by BAT3.
过氧化物酶体睾丸特异性 1 基因 (Pxt1) 是迄今为止已知的唯一编码过氧化物酶体蛋白的雄性生殖细胞特异性基因。为了阐明 Pxt1 在精子发生中的作用,我们生成了表达 c-MYC-PXT1 融合蛋白的转基因小鼠,该蛋白受 PGK2 启动子的控制。Pxt1 的过表达导致主要在初级精母细胞中诱导雄性生殖细胞凋亡,最终导致男性不育。这促使我们分析了具有 N 端 BH3 样结构域的小鼠 PXT1 的促凋亡特性。在不同的细胞系中,PXT1 的过表达也导致细胞凋亡的急剧增加,而 BH3 样结构域的缺失则显著减少了细胞死亡事件,从而证实该结构域是 PXT1 促凋亡活性所必需的和功能性的。此外,我们证明了 PXT1 与凋亡调节剂 BAT3 相互作用,如果过表达,BAT3 可以保护细胞免受 PXT1 诱导的凋亡。PXT1-BAT3 的相互作用导致 PXT1 从细胞质向细胞核转移。总之,我们证明了 PXT1 通过 BH3 样结构域诱导细胞凋亡,而这个过程被 BAT3 抑制。