Li B, Luo H, Weng Q, Wang S, Pan Z, Xie Z, Wu W, Liu H, Li Q
College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.
Reprod Domest Anim. 2016 Dec;51(6):1030-1038. doi: 10.1111/rda.12794. Epub 2016 Sep 22.
FK506-binding protein 6 (FKBP6) is essential for meiosis during mammalian spermatogenesis. However, the molecular regulation of FKBP6 during spermatogenesis remains unclear. In the present study, we performed molecular characterization of the meiosis-specific gene FKBP6 in yak testes. Yak FKBP6 encodes a polypeptide of 295 amino acid residues with an FK506-binding domain (FKBP_C) and three tetratricopeptide repeat domains. The methylation level of the FKBP6 promoter in testes was significantly higher in cattle-yak with male sterility than in yak, and the FKBP6 promoter was methylated in liver tissues in which FKBP6 is not expressed. FKBP6 promoter activity was significantly decreased after treatment with the M.SssI methyltransferase in vitro. Furthermore, the FKBP6 gene was remarkably activated in bovine mammary epithelial cells treated with the DNA methyltransferase inhibitor 5-aza-2-deoxycytidine. Taken together, our results demonstrate for the first time that the FKBP6 promoter is differentially methylated in testes; together with the functional promoter analysis, this suggests that methylation of this promoter may contribute to cattle-yak male infertility.
FK506结合蛋白6(FKBP6)对哺乳动物精子发生过程中的减数分裂至关重要。然而,精子发生过程中FKBP6的分子调控仍不清楚。在本研究中,我们对牦牛睾丸中减数分裂特异性基因FKBP6进行了分子特征分析。牦牛FKBP6编码一个由295个氨基酸残基组成的多肽,具有一个FK506结合结构域(FKBP_C)和三个四肽重复结构域。雄性不育的犏牛睾丸中FKBP6启动子的甲基化水平显著高于牦牛,且在不表达FKBP6的肝脏组织中FKBP6启动子发生了甲基化。体外经M.SssI甲基转移酶处理后,FKBP6启动子活性显著降低。此外,在用DNA甲基转移酶抑制剂5-氮杂-2'-脱氧胞苷处理的牛乳腺上皮细胞中,FKBP6基因被显著激活。综上所述,我们的结果首次证明FKBP6启动子在睾丸中存在差异甲基化;结合启动子功能分析,这表明该启动子的甲基化可能导致犏牛雄性不育。