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From the * Department of Medical Chemistry, Kansai
Medical University, Moriguchi, Japan; and the
Department of Urology and Andrology, Kansai
Medical University, Hirakata, Japan.
| Correspondence to: Dr Seiji Ito, Department of Medical Chemistry, Kansai Medical University, 10-15 Fumizono, Moriguchi, Osaka 570-8506, Japan (e-mail: ito{at}takii.kmu.ac.jp). |
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.
Key words: Fertilization, gene regulation, meiosis, spermatogenesis, testis
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