Chizaki Ryusuke, Yao Ikuko, Katano Tayo, Matsuda Tadashi, Ito Seiji
Department of Medical Chemistry, Kansai Medical University, 10-15 Fumizono, Moriguchi, Osaka 570-8506, Japan.
J Androl. 2012 Mar-Apr;33(2):277-86. doi: 10.2164/jandrol.110.012294. Epub 2011 Jun 2.
The development of multicellular organisms is controlled by sequential activation of a hierarchy of regulatory genes, which encode transcription factors having DNA-binding motifs. We previously identified a testis-specific zinc finger transcriptional factor, Ovol2/MOVO, as a mouse homologue of Drosophila Ovo. Because mice deficient in Ovol2/Movo die during early embryogenesis, its function in male germ cells has remained unknown. We have recently succeeded in preparing anti-Ovol2/MOVO antiserum for immunohistochemical use. In the present study, we demonstrated that Ovol2/MOVO protein started to be expressed in male germ cells at 2 weeks after birth and that Ovol2/MOVO expression was restricted to the XY body in spermatocytes at the pachytene stage. In a reporter assay, Ovol2/MOVO repressed the histone H1t promoter activity in the spermatogenic cell line GC-2spd. These results suggest that Ovol2/MOVO may play an important role in the XY body during spermatogenesis, possibly in the processes of XY body formation and meiotic sex chromosome inactivation.
多细胞生物的发育由调控基因层级的顺序激活所控制,这些调控基因编码具有DNA结合基序的转录因子。我们之前鉴定出一种睾丸特异性锌指转录因子Ovol2/MOVO,它是果蝇Ovo的小鼠同源物。由于Ovol2/Movo基因缺失的小鼠在胚胎发育早期死亡,其在雄性生殖细胞中的功能一直未知。我们最近成功制备了用于免疫组织化学的抗Ovol2/MOVO抗血清。在本研究中,我们证明Ovol2/MOVO蛋白在出生后2周开始在雄性生殖细胞中表达,并且Ovol2/MOVO的表达在粗线期精母细胞中局限于XY体。在报告基因检测中,Ovol2/MOVO抑制了生精细胞系GC-2spd中的组蛋白H1t启动子活性。这些结果表明,Ovol2/MOVO可能在精子发生过程中的XY体中发挥重要作用,可能参与XY体形成和减数分裂性染色体失活过程。