Department of Biology, Waseda University, Wakamatsu-cho, Shinjuku-ku, Tokyo, Japan.
Comp Biochem Physiol B Biochem Mol Biol. 2011 Sep;160(1):54-61. doi: 10.1016/j.cbpb.2011.05.008. Epub 2011 Jun 2.
CYP17A1 expression is up-regulated in the gonad in Rana (Glandirana) rugosa tadpoles treated with androgens to induce female-to-male sex-reversal. In this study, we isolated the CYP17A1 gene and its processed pseudogene from R. rugosa. The former was found to consist of 8 exons, and the latter a single-exon gene, designated CYP17A1P. The sequence of the promoter region of CYP17A1 differed from that of CYP17A1P. We found several consensus binding-sites for candidate transcription factors including androgen receptor (AR), Sox and FoxL2 in the CYP17A1 promoter region, but an AR-binding site was absent from CYP17A1P. When AR was over-expressed in Xenopus A6 cells, it did not increase CYP17A1 transcription in luciferase assays. CYP17A1 was strongly expressed in indifferent male gonads during sex determination and exclusively in testis, among eight adult tissues of R. rugosa. By contrast, CYP17A1P was expressed at very low, and similar levels in the adult tissues of both sexes. Fluorescent In-Situ Hybridization (FISH) analysis showed that CYP17A1P is localized to chromosome 4, while CYP17A1 is on chromosome 9. These results collectively suggest that CYP17A1, but not CYP17A1P is involved in male sex-determination in R. rugosa, and that androgens may not have a direct effect on the CYP17A1 transcription.
CYP17A1 的表达在受到雄激素处理的中华大蟾蜍(Glandirana)蝌蚪的性腺中被上调,以诱导雌性到雄性的性别反转。在本研究中,我们从中华大蟾蜍中分离出 CYP17A1 基因及其加工假基因。前者由 8 个外显子组成,后者为单外显子基因,命名为 CYP17A1P。CYP17A1 的启动子区域序列与 CYP17A1P 不同。我们在 CYP17A1 启动子区域发现了几个候选转录因子(包括雄激素受体(AR)、Sox 和 FoxL2)的结合位点,但 CYP17A1P 中没有 AR 结合位点。当 AR 在非洲爪蟾 A6 细胞中过表达时,它不会增加荧光素酶检测中的 CYP17A1 转录。CYP17A1 在性别决定期间在两性未分化的雄性性腺中强烈表达,而在中华大蟾蜍的 8 种成年组织中仅在睾丸中表达。相比之下,CYP17A1P 在两性成年组织中的表达水平非常低且相似。荧光原位杂交(FISH)分析表明,CYP17A1P 定位于染色体 4,而 CYP17A1 定位于染色体 9。这些结果共同表明,CYP17A1 而不是 CYP17A1P 参与了中华大蟾蜍的雄性性别决定,并且雄激素可能对 CYP17A1 转录没有直接影响。