Goto Teppei, Tomikawa Junko, Ikegami Kana, Minabe Shiori, Abe Hitomi, Fukanuma Tatsuya, Imamura Takuya, Takase Kenji, Sanbo Makoto, Tomita Koichi, Hirabayashi Masumi, Maeda Kei-ichiro, Tsukamura Hiroko, Uenoyama Yoshihisa
Graduate School of Bioagricultural Sciences (T.G., J.T., K.I., S.M., H.A., T.F., K.Ta., H.T., Y.U.), Nagoya University, Nagoya 464-8601, Japan; National Institute for Physiological Sciences (T.G., M.S., K.To., M.H.), Okazaki 444-8585, Japan; Graduate School of Medical Sciences (T.I.), Kyushu University, Fukuoka 812-8581, Japan; Kochi Medical School (K.To.), Kochi University, Kochi 783-8505, Japan; and Graduate School of Agricultural and Life Sciences (K.M.), The University of Tokyo, Tokyo 113-8657, Japan.
Mol Endocrinol. 2015 Jan;29(1):121-9. doi: 10.1210/me.2014-1289.
Pulsatile secretion of GnRH plays a pivotal role in follicular development via stimulating tonic gonadotropin secretion in mammals. Kisspeptin neurons, located in the arcuate nucleus (ARC), are considered to be an intrinsic source of the GnRH pulse generator. The present study aimed to determine ARC-specific enhancer(s) of the Kiss1 gene by an in vivo reporter assay. Three green fluorescent protein (GFP) reporter constructs (long, medium length, and short) were generated by insertion of GFP cDNA at the Kiss1 locus. Transgenic female mice bearing the long and medium-length constructs showed apparent GFP signals in kisspeptin-immunoreactive cells in both the ARC and anteroventral periventricular nucleus, in which another population of kisspeptin neurons are located. On the other hand, transgenic mice bearing 5'-truncated short construct showed few GFP signals in the ARC kisspeptin-immunoreactive cells, whereas they showed colocalization of GFP- and kisspeptin-immunoreactivities in the anteroventral periventricular nucleus. In addition, chromatin immunoprecipitation and chromosome conformation capture assays revealed recruitment of unoccupied estrogen receptor-α in the 5'-upstream region and intricate chromatin loop formation between the 5'-upstream and promoter regions of Kiss1 locus in the ARC. Taken together, the present results indicate that 5'-upstream region of Kiss1 locus plays a critical role in Kiss1 gene expression in an ARC-specific manner and that the recruitment of estrogen receptor-α and formation of a chromatin loop between the Kiss1 promoter and the 5' enhancer region may be required for the induction of ARC-specific Kiss1 gene expression. These results suggest that the 5'-upstream region of Kiss1 locus functions as an enhancer for ARC Kiss1 gene expression in mice.
促性腺激素释放激素(GnRH)的脉冲式分泌通过刺激哺乳动物的促性腺激素持续性分泌,在卵泡发育中起关键作用。位于弓状核(ARC)的 kisspeptin 神经元被认为是 GnRH 脉冲发生器的内在来源。本研究旨在通过体内报告基因测定法确定 Kiss1 基因的 ARC 特异性增强子。通过在 Kiss1 基因座插入绿色荧光蛋白(GFP)cDNA,构建了三种绿色荧光蛋白报告基因构建体(长、中、短)。携带长和中等长度构建体的转基因雌性小鼠在 ARC 和室周前腹核的 kisspeptin 免疫反应性细胞中显示出明显的 GFP 信号,室周前腹核中也存在另一群 kisspeptin 神经元。另一方面,携带 5' 截短短构建体的转基因小鼠在 ARC kisspeptin 免疫反应性细胞中显示出很少的 GFP 信号,而它们在室周前腹核中显示出 GFP 和 kisspeptin 免疫反应性的共定位。此外,染色质免疫沉淀和染色体构象捕获分析揭示了在 5' 上游区域未占据的雌激素受体-α 的募集以及 ARC 中 Kiss1 基因座的 5' 上游和启动子区域之间复杂的染色质环形成。综上所述,本研究结果表明 Kiss1 基因座的 5' 上游区域以 ARC 特异性方式在 Kiss1 基因表达中起关键作用,并且雌激素受体-α 的募集以及 Kiss1 启动子和 5' 增强子区域之间染色质环的形成可能是诱导 ARC 特异性 Kiss1 基因表达所必需的。这些结果表明 Kiss1 基因座的 5' 上游区域在小鼠中作为 ARC Kiss1 基因表达的增强子发挥作用。