Nakaya Yuki, Kizaki Keiichiro, Takahashi Toru, Patel Osman V, Hashizume Kazuiyoshi
Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
BMC Mol Biol. 2009 Mar 5;10:19. doi: 10.1186/1471-2199-10-19.
Bovine trophoblast binucleate cells (BNC) express a plethora of molecules including bovine placental lactogen (bPL, gene name is bCSH1) and bovine prolactin-related protein-1 (bPRP1). BCSH1 and bPRP1 are members of the growth hormone (GH)/prolactin (PRL) gene family, which are expressed simultaneously in BNC and are central to placentation and the progression of pregnancy in cattle. However, there is a paucity of information on the transcriptional regulatory mechanisms of both the bCSH1 and bPRP1 genes. Recent studies, however, have demonstrated that the expression of a number of genes is controlled by the methylation status of their promoter region. In the present study, we examined the cell-type-specific epigenetic alterations of the 5'-flanking region of the bCSH1 and bPRP1 genes to gain an insight into their regulatory mechanisms.
Analysis of 5-aza-2'-deoxycytidine treatment demonstrated that bCSH1 expression is moderately induced in fibroblast cultures but enhanced in BT-1 cells. Sodium bisulfite based sequencing revealed that bCSH1 is hypomethylated in the cotyledonary tissue but not in the fetal skin, and this pattern was not altered with the progression of pregnancy. On the other hand, the methylation status of bPRP1 was similar between the cotyledon and fetal skin. The bPRP1 gene was exclusively hypermethylated in a bovine trophoblast cell-derived BT-1 cell-line. While the activity of bCSH1 was similar in both BT-1 and bovine fibroblast cells, that of bPRP1 was specific to BT-1. Treatment with a demethylating agent and luciferase assays provided in vitro evidence of the positive regulation of bCSH1 but not bPRP1.
This is the first report to identify the differential regulatory mechanisms of the bCSH1 and bPRP1 genes and indicates that bCSH1 might potentially be the only transcript that is subject to DNA methyltransferase regulation. The data indicates the possibility of novel kinetics of induction of the synchronously expressed BNC-specific bCSH1 and bPRP1 transcripts, which may aid the understanding of the intricate regulation and specific role(s) of these important molecules in bovine placentogenesis and the progression of pregnancy.
牛滋养层双核细胞(BNC)表达大量分子,包括牛胎盘催乳素(bPL,基因名称为bCSH1)和牛催乳素相关蛋白-1(bPRP1)。BCSH1和bPRP1是生长激素(GH)/催乳素(PRL)基因家族的成员,它们在BNC中同时表达,并且对牛的胎盘形成和妊娠进展至关重要。然而,关于bCSH1和bPRP1基因的转录调控机制的信息却很少。然而,最近的研究表明,许多基因的表达受其启动子区域甲基化状态的控制。在本研究中,我们研究了bCSH1和bPRP1基因5'-侧翼区域的细胞类型特异性表观遗传改变,以深入了解它们的调控机制。
对5-氮杂-2'-脱氧胞苷处理的分析表明,bCSH1在成纤维细胞培养物中受到中度诱导,但在BT-1细胞中增强。基于亚硫酸氢钠的测序显示,bCSH1在子叶组织中低甲基化,但在胎儿皮肤中不低甲基化,并且这种模式不会随着妊娠进展而改变。另一方面,bPRP1在子叶和胎儿皮肤之间的甲基化状态相似。bPRP1基因在牛滋养层细胞衍生的BT-1细胞系中完全高甲基化。虽然bCSH1在BT-1细胞和牛成纤维细胞中的活性相似,但bPRP1的活性对BT-1细胞具有特异性。用去甲基化剂处理和荧光素酶测定提供了bCSH1而非bPRP1正向调控体外证据。
这是第一份鉴定bCSH1和bPRP1基因差异调控机制的报告,并表明bCSH1可能是唯一受DNA甲基转移酶调控的转录本。数据表明同步表达的BNC特异性bCSH1和bPRP1转录本诱导新动力学的可能性,这可能有助于理解这些重要分子在牛胎盘形成和妊娠进展中的复杂调控和特定作用。