Controlling Trophoblast Cell Fusion in the Human Placenta-Transcriptional Regulation of Suppressyn, an Endogenous Inhibitor of Syncytin-1

被引:6
作者
Sugimoto, Jun [1 ]
Schust, Danny J. [2 ]
Sugimoto, Makiko [1 ]
Jinno, Yoshihiro [3 ]
Kudo, Yoshiki [1 ]
机构
[1] Hiroshima Univ, Grad Sch Med Sci, Dept Obstet & Gynecol, Hiroshima 7348551, Japan
[2] Duke Univ, Dept Obstet & Gynecol, Durham, NC 27710 USA
[3] Univ Ryukyus, Dept Mol Biol, Nishihara, Okinawa 9030215, Japan
关键词
suppressyn; syncytin; HERV; placenta; cell fusion; promoter; DNA methylation; hypoxia inducible factor (HIF); HYPOXIA INDUCIBLE FACTORS; GENE-EXPRESSION; 1ST TRIMESTER; GATA FACTORS; OXYGEN; METHYLATION; DIFFERENTIATION; EVOLUTION; ENHANCER; PROTEIN;
D O I
10.3390/biom13111627
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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, ERVH48-1, and examined their regulation via DNA methylation and their responses to changes in the oxygen concentration. Like other endogenous retroviral genes, the ERVH48-1 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 ERVH48-1 is tightly controlled by DNA methylation and further regulated by oxygen concentration-dependent, hypoxia-induced transcription factors (HIF1 alpha and HIF2 alpha). 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 HIF1 alpha and HIF2 alpha. 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.
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页数:15
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