Laboratory of Veterinary Biochemistry and Molecular Biology, Graduate School of Medicine and Veterinary Medicine/Faculty of Agriculture, University of Miyazaki, 1-1 Gakuen-Kibanadai-Nishi, Miyazaki 889-2192, Japan.
Present address: Division of Molecular Modification and Cancer Biology, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
J Vet Med Sci. 2020 Jun 16;82(6):681-689. doi: 10.1292/jvms.20-0050. Epub 2020 Apr 2.
Steroidogenic factor 1 (SF-1) is a nuclear receptor that is important in steroid hormone production, and adrenal and gonad development. The SF-1 gene is highly conserved among most vertebrates. However, dog SF-1 registered in public databases, such as CanFam3.1, lacks the 5' end compared to other mammals including mouse, human, bovine, and cat. Whether this defect is due to species differences or database error is unclear. Here, we determined the full-length dog SF-1 cDNA sequence and identified the missing 5' end sequence in the databases. The coding region of the dog SF-1 gene has 1,386 base pairs, and the protein has 461 amino acid residues. Sequence alignment analysis among vertebrates revealed that the 5' end sequence of dog SF-1 cDNA is highly conserved compared to other vertebrates. The genomic position of the first exon was determined, and its promoter region sequence was analyzed. The DNA methylation state at the basal promoter and the expression of dog SF-1 in steroidogenic tissues and non-steroidogenic cells were examined. CpG sites at the basal promoter displayed methylation kinetics inversely correlated with gene expression. The promoter was hypomethylated and hypermethylated in SF-1 expressing and non-SF-1 expressing tissues, respectively. In conclusion, we identified the true full sequence of dog SF-1 cDNA and determined the genome sequence around the first exon. The gene is under the control of epigenetic regulation, such as DNA methylation, at the promoter.
类固醇生成因子 1(SF-1)是一种核受体,在类固醇激素产生、肾上腺和性腺发育中具有重要作用。SF-1 基因在大多数脊椎动物中高度保守。然而,与包括小鼠、人类、牛和猫在内的其他哺乳动物相比,公共数据库(如 CanFam3.1)中注册的犬 SF-1 基因缺失了 5'端。这种缺陷是由于物种差异还是数据库错误尚不清楚。在这里,我们确定了犬 SF-1 cDNA 的全长序列,并在数据库中鉴定出缺失的 5'端序列。犬 SF-1 基因的编码区有 1386 个碱基对,蛋白质有 461 个氨基酸残基。脊椎动物之间的序列比对分析表明,与其他脊椎动物相比,犬 SF-1 cDNA 的 5'端序列高度保守。确定了第一个外显子的基因组位置,并分析了其启动子序列。研究了基础启动子处的 DNA 甲基化状态以及犬 SF-1 在类固醇生成组织和非类固醇生成细胞中的表达。基础启动子处的 CpG 位点的甲基化动力学与基因表达呈负相关。在 SF-1 表达和非 SF-1 表达组织中,启动子分别呈低甲基化和高甲基化状态。总之,我们确定了犬 SF-1 cDNA 的真实全长序列,并确定了第一个外显子周围的基因组序列。该基因受启动子处的表观遗传调控,如 DNA 甲基化的调控。