Key Laboratory of Agricultural Animal Genetics, Breeding, and Reproduction of Ministry of Education and Key Laboratory of Swine Genetics and Breeding of Ministry of Agriculture, Huazhong Agricultural University, Wuhan, 430070, Hubei, People's Republic of China.
Mol Cell Biochem. 2013 Feb;374(1-2):213-22. doi: 10.1007/s11010-012-1522-5. Epub 2012 Nov 18.
Homeobox A10 (HOXA10), a well-known transcriptional factor that can be regulated by estrogen (E(2)) and progesterone (P(4)), is necessary not only for endometrial differentiation but also for establishing the conditions required for implantation. However, little research has focused on the regulation of the porcine HOXA10 gene. In this study, we aimed to (1) characterize the genetic structure of the porcine HOXA10 gene, (2) analyze the tissue expression pattern and differential expression levels in the endometrium of HOXA10 in different developmental stages of Meishan and commercial Yorkshire pigs, and (3) identify the E2/P4 response element in the promoter region of the porcine HOXA10 gene and verify that it induces HOXA10 in human endometrial adenocarcinoma (Ishikawa) cells. The results indicated that the cDNA of porcine HOXA10 was 2,628 bp in length with an open reading frame (ORF) of 1,236 bp encoding a peptide of 411-amino acid residues, which showed 90 and 95 % sequence similarity to that of human and mouse homologs, respectively. Semiquantitative RT-PCR confirmed that the porcine HOXA10 gene is highly expressed in the endometrium, bladder and kidney. Real-time PCR showed that the expression of HOXA10 was significantly higher on day 15 of gestation (gd 15) in comparison to gd 26 (P < 0.01), gd 50 (P < 0.01) and day 15 of the estrous cycle (ed 15) in the endometrium of Meishan pigs. In contrast, the highest expression in the endometrium of Yorkshire pigs was on gd 50. Moreover, the abundance of HOXA10 mRNA was the highest on gd 15 in Meishan pigs than in any other stage tested in the two breeds. Deletion analysis and reporter expression assays identified a promoter region (-1044 bp to +18 bp) which is responsible for E(2)- and P(4)-induced HOXA10 transcription. Moreover, this promoter region enhanced the E2/P4-induced HOXA10 expression in Ishikawa cells. In conclusion, we identified an E(2)/P(4) response element of the porcine HOXA10 gene for the first time. The data from the present study contribute to the mechanism by which the porcine HOXA10 gene regulates embryo implantation and prolificacy traits.
同源盒 A10(HOXA10)是一种众所周知的转录因子,可被雌激素(E2)和孕激素(P4)调节,不仅对子宫内膜分化是必需的,而且对建立植入所需的条件也是必需的。然而,很少有研究关注猪 HOXA10 基因的调控。在这项研究中,我们旨在:(1)描述猪 HOXA10 基因的遗传结构;(2)分析 HOXA10 在不同发育阶段梅山和商业约克夏猪子宫内膜中的组织表达模式和差异表达水平;(3)鉴定猪 HOXA10 基因启动子区的 E2/P4 反应元件,并验证其在人子宫内膜腺癌(Ishikawa)细胞中诱导 HOXA10。结果表明,猪 HOXA10 的 cDNA 长 2628bp,开放阅读框(ORF)长 1236bp,编码 411 个氨基酸残基的肽,分别与人源和鼠源同源物的序列相似性为 90%和 95%。半定量 RT-PCR 证实猪 HOXA10 基因在子宫内膜、膀胱和肾脏中高度表达。实时 PCR 显示,与 gd26(P<0.01)、gd50(P<0.01)和发情周期 ed15(P<0.01)相比,梅山猪妊娠第 15 天(gd15)子宫内膜中 HOXA10 的表达显著升高。相比之下,在约克夏猪子宫内膜中,表达量最高的是 gd50。此外,在梅山猪中,HOXA10 mRNA 的丰度在 gd15 时高于两个品种的任何其他阶段。缺失分析和报告基因表达试验鉴定了一个负责 E2 和 P4 诱导 HOXA10 转录的启动子区域(-1044bp 到+18bp)。此外,该启动子区域增强了 Ishikawa 细胞中 E2/P4 诱导的 HOXA10 表达。总之,我们首次鉴定了猪 HOXA10 基因的 E2/P4 反应元件。本研究的数据有助于了解猪 HOXA10 基因调节胚胎着床和繁殖性状的机制。