| Literature DB >> 24006281 |
Shunsuke Kuroki1, Mika Akiyoshi, Mikiyo Tokura, Hitoshi Miyachi, Yuji Nakai, Hiroshi Kimura, Yoichi Shinkai, Makoto Tachibana.
Abstract
JmjC domain-containing proteins are a class of enzymes responsible for histone demethylation. Previous studies revealed that the JmjC domain-containing protein KDM3A possesses intrinsic demethylase activity toward lysine 9 of histone H3 and plays essential roles in spermiogenesis. In contrast, the biological roles of JMJD1C, a KDM3A homolog in mice, are largely unknown. Here we present the crucial role of JMJD1C in male gametogenesis. Jmjd1c-deficient males became infertile due to the progressive reduction of germ cells after 3 mo of age. Importantly, Jmjd1c-deficient testes frequently contained abnormal tubules lacking developmentally immature germ cells. JMJD1C is most abundantly expressed in undifferentiated spermatogonia in mouse testis. The numbers of ZBTB16-positive spermatogonia and apoptotic germ cells in Jmjd1c-deficient testes decreased and increased in an age-dependent manner, respectively. Our studies demonstrated that JMJD1C contributes to the long-term maintenance of the male germ line.Entities:
Keywords: aging; epigenetics; histone modifications; male infertility
Mesh:
Substances:
Year: 2013 PMID: 24006281 DOI: 10.1095/biolreprod.113.108597
Source DB: PubMed Journal: Biol Reprod ISSN: 0006-3363 Impact factor: 4.285