Department of Obstetrics and Gynecology, Graduate School of Medical Sciences, Hiroshima University, Hiroshima 734-8551, Japan.
Department of Obstetrics and Gynecology, Duke University, Durham, NC 27710, USA.
Biomolecules. 2023 Nov 7;13(11):1627. doi: 10.3390/biom13111627.
Cell fusion in the placenta is tightly regulated. Suppressyn is a human placental endogenous retroviral protein that inhibits the profusogenic activities of another well-described endogenous retroviral protein, syncytin-1. In this study, we aimed to elucidate the mechanisms underlying suppressyn's placenta-specific expression. We identified the promoter region and a novel enhancer region for the gene encoding suppressyn, , and examined their regulation via DNA methylation and their responses to changes in the oxygen concentration. Like other endogenous retroviral genes, the promoter sequence is found within a characteristic retroviral 5' LTR sequence. The novel enhancer sequence we describe here is downstream of this LTR sequence (designated EIEs: ERV internal enhancer sequence) and governs placental expression. The placenta-specific expression of is tightly controlled by DNA methylation and further regulated by oxygen concentration-dependent, hypoxia-induced transcription factors (HIF1α and HIF2α). Our findings highlight the involvement of (1) tissue specificity through DNA methylation, (2) expression specificity through placenta-specific enhancer regions, and (3) the regulation of suppressyn expression in differing oxygen conditions by HIF1α and HIF2α. We suggest that these regulatory mechanisms are central to normal and abnormal placental development, including the development of disorders of pregnancy involving altered oxygenation, such as preeclampsia, pregnancy-induced hypertension, and fetal growth restriction.
胎盘细胞融合受到严格调控。Suppressyn 是一种人类胎盘内源性逆转录病毒蛋白,可抑制另一种已被充分描述的内源性逆转录病毒蛋白 Syncytin-1 的增殖活性。在这项研究中,我们旨在阐明 Suppressyn 胎盘特异性表达的机制。我们鉴定了编码 Suppressyn 的基因的启动子区域和一个新的增强子区域,并通过 DNA 甲基化检查了它们的调控及其对氧浓度变化的反应。与其他内源性逆转录病毒基因一样,该基因的启动子序列位于特征性逆转录病毒 5'LTR 序列内。我们在此描述的新增强子序列位于该 LTR 序列的下游(指定为 EIEs:内源性逆转录病毒内部增强子序列),并负责胎盘表达。通过 DNA 甲基化和受氧浓度依赖性缺氧诱导转录因子(HIF1α 和 HIF2α)调控,对 的胎盘特异性表达进行严格控制。我们的发现强调了(1)通过 DNA 甲基化实现组织特异性,(2)通过胎盘特异性增强子区域实现表达特异性,以及(3)HIF1α 和 HIF2α 对 Suppressyn 表达在不同氧条件下的调节。我们认为,这些调节机制是正常和异常胎盘发育的核心,包括涉及氧合改变的妊娠并发症的发展,如子痫前期、妊娠高血压和胎儿生长受限。