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滋养层特异性元件结合蛋白对人绒毛膜促性腺激素α亚基和β亚基基因的协同调控

Coordinate control of the alpha- and beta-subunit genes of human chorionic gonadotropin by trophoblast-specific element-binding protein.

作者信息

Steger D J, Büscher M, Hecht J H, Mellon P L

机构信息

Department of Reproductive Medicine, University of California-San Diego, La Jolla 92093.

出版信息

Mol Endocrinol. 1993 Dec;7(12):1579-88. doi: 10.1210/mend.7.12.7511787.

Abstract

The alpha- and beta-subunit genes of hCG are coordinately regulated in the trophectoderm of the early embryo and placenta. Placenta-specific expression of the alpha-subunit gene is determined by a composite enhancer made of three clustered components: cAMP-responsive elements, a GATA site, and the trophoblast-specific element (TSE). We have investigated the basis of placenta-specific expression of the major hCG beta-subunit gene, hCG beta 5. Enhancement of expression localizes to the region from -305 to -279, whereas full cAMP regulation requires the region from -305 to -249. Four DNAse-I footprints are present, three of which can be competed by the TSE element from the alpha-subunit gene. Methylation interference establishes that binding to the element located in the key region for expression, from -301 to -275, requires contacts with a CCNNNGGG core sequence that matches the alpha-subunit gene TSE. Sequence-specific DNA affinity chromatography using the alpha-subunit gene TSE allows purification of TSE-binding protein. This purified protein binds specifically to the key element, -301 to -275, and to at least two additional TSE elements clustered in the regulatory region of the hCG beta 5 gene. We conclude that both the alpha- and beta-subunit genes of hCG require the placenta-specific factor TSE-binding protein for expression, providing a mechanism for their coordinate regulation in placental cells.

摘要

人绒毛膜促性腺激素(hCG)的α亚基和β亚基基因在早期胚胎和胎盘的滋养外胚层中受到协同调控。α亚基基因的胎盘特异性表达由一个由三个成簇元件组成的复合增强子决定:环磷酸腺苷(cAMP)反应元件、一个GATA位点和滋养层特异性元件(TSE)。我们研究了主要的hCG β亚基基因hCG β5胎盘特异性表达的基础。表达增强定位于-305至-279区域,而完整的cAMP调控则需要-305至-249区域。存在四个脱氧核糖核酸酶I(DNAse-I)足迹,其中三个可以被α亚基基因的TSE元件竞争。甲基化干扰表明,与位于表达关键区域(从-301至-275)的元件结合需要与一个与α亚基基因TSE匹配的CCNNNGGG核心序列接触。使用α亚基基因TSE进行序列特异性DNA亲和层析可纯化TSE结合蛋白。这种纯化的蛋白特异性结合关键元件-301至-275,以及hCG β5基因调控区域中聚集的至少两个额外的TSE元件。我们得出结论,hCG的α亚基和β亚基基因表达均需要胎盘特异性因子TSE结合蛋白,这为它们在胎盘细胞中的协同调控提供了一种机制。

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