Animal Biotechnology, Graduate School of Bio & Information Technology, Institute of Genetic Engineering, Hankyong National University, Ansung 456-749, Korea.
Reprod Biol Endocrinol. 2011 Oct 20;9:139. doi: 10.1186/1477-7827-9-139.
The aldo-keto reductase family 1 member C1 (AKR1C1) belongs to a superfamily of NADPH-dependent reductases that convert a wide range of substrates, including carbohydrates, steroid hormones, and endogenous prostaglandins. The 20 alpha-hydroxysteroid dehydrogenase (20 alpha-HSD) is a member of AKR family. The aims of this study were to determine its expression in the ovary and uterus endometrium during the estrous cycle and pregnancy.
Rapid amplification of cDNA ends (RACE) experiments were performed to obtain the 5' and 3' ends of the porcine 20 alpha-HSD cDNA. Reverse-transcriptase-PCR (RT-PCR), real-time PCR, northern blot analysis, and western blot analysis were performed to examine the expression of porcine 20 alpha-HSD. Immunohistochemical analysis was also performed to determine the localization in the ovary.
The porcine 20 alpha-HSD cDNA is 957 bp in length and encodes a protein of 319 amino acids. The cloned cDNA was virtually the same as the porcine AKR1C1 gene (337 amino acids) reported recently, and only differed in the C-terminal region (the AKR1C1 gene has a longer C-terminal region than our sequence). The 20 alpha-HSD gene (from now on referred to as AKR1C1) cloned in this paper encodes a deletion of 4 amino acids, compared with the C-terminal region of AKR1C1 genes from other animals. Porcine AKR1C1 mRNA was expressed on day 5, 10, 12, 15 of the cycle and 0-60 of pregnancy in the ovary. The mRNA was also specifically detected in the uterine endometrium on day 30 of pregnancy. Western blot analysis indicated that the pattern of AKR1C1 protein in the ovary during the estrous cycle and uterus during early pregnancy was similar to that of AKR1C1 mRNA expression. The recombinant protein produced in CHO cells was detected at approximately 37 kDa. Immunohistochemical analysis also revealed that pig AKR1C1 protein was localized in the large luteal cells in the early stages of the estrous cycle and before parturition.
Our study demonstrated that AKR1C1 mRNA and protein are coordinately expressed in the luteal cell of ovary throughout the estrous cycle and in the uterus on day 30 of pregnancy. Thus, the porcine AKR1C1 gene might control important mechanisms during the estrous cycle.
醛酮还原酶家族 1 成员 C1(AKR1C1)属于 NADPH 依赖性还原酶超家族,可将包括碳水化合物、甾体激素和内源性前列腺素在内的广泛底物转化。20α-羟类固醇脱氢酶(20α-HSD)是 AKR 家族的成员。本研究的目的是确定其在发情周期和妊娠期间在卵巢和子宫子宫内膜中的表达。
进行快速扩增 cDNA 末端(RACE)实验以获得猪 20α-HSD cDNA 的 5'和 3'末端。进行逆转录-聚合酶链反应(RT-PCR)、实时 PCR、northern blot 分析和 western blot 分析以检查猪 20α-HSD 的表达。还进行了免疫组织化学分析以确定在卵巢中的定位。
猪 20α-HSD cDNA 长 957bp,编码 319 个氨基酸的蛋白质。克隆的 cDNA 与最近报道的猪 AKR1C1 基因(337 个氨基酸)几乎相同,仅在 C 末端区域不同(AKR1C1 基因的 C 末端区域比我们的序列长)。本文克隆的 20α-HSD 基因(以下简称 AKR1C1)与来自其他动物的 AKR1C1 基因的 C 末端区域相比,编码 4 个氨基酸的缺失。猪 AKR1C1mRNA 在发情周期的第 5、10、12、15 天和妊娠的 0-60 天在卵巢中表达。在妊娠第 30 天的子宫子宫内膜中也特异性检测到该 mRNA。Western blot 分析表明,发情周期中卵巢和早孕时子宫的 AKR1C1 蛋白表达模式与 AKR1C1mRNA 表达模式相似。在 CHO 细胞中产生的重组蛋白检测到约 37kDa。免疫组织化学分析还表明,猪 AKR1C1 蛋白定位于发情周期早期的大黄体细胞和分娩前。
我们的研究表明,AKR1C1mRNA 和蛋白在发情周期中卵巢的黄体细胞中以及妊娠第 30 天的子宫中协调表达。因此,猪 AKR1C1 基因可能控制发情周期中的重要机制。