首页> 美国卫生研究院文献>Molecular and Cellular Biology >Expression of the glycoprotein hormone alpha-subunit gene in the placenta requires a functional cyclic AMP response element whereas a different cis-acting element mediates pituitary-specific expression.
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Expression of the glycoprotein hormone alpha-subunit gene in the placenta requires a functional cyclic AMP response element whereas a different cis-acting element mediates pituitary-specific expression.

机译:糖蛋白激素α-亚基基因在胎盘中的表达需要功能性的环状AMP反应元件而不同的顺式作用元件介导垂体特异性表达。

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摘要

The single-copy gene encoding the alpha subunit of glycoprotein hormones is expressed in the pituitaries of all mammals and in the placentas of only primates and horses. We have systematically analyzed the promoter-regulatory elements of the human and bovine alpha-subunit genes to elucidate the molecular mechanisms underlying their divergent patterns of tissue-specific expression. This analysis entailed the use of transient expression assays in a chorionic gonadotropin-secreting human choriocarcinoma cell line, protein-DNA binding assays, and expression of chimeric forms of human or bovine alpha subunit genes in transgenic mice. From the results, we conclude that placental expression of the human alpha-subunit gene requires a functional cyclic AMP response element (CRE) that is present as a tandem repeat in the promoter-regulatory region. In contrast, the promoter-regulatory region of the bovine alpha-subunit gene, as well as of the rat and mouse genes, was found to contain a single CRE homolog that differed from its human counterpart by a single nucleotide. This difference substantially reduced the binding affinity of the bovine CRE homolog for the nuclear protein that bound to the human alpha CRE and thereby rendered the bovine alpha-subunit promoter inactive in human choriocarcinoma cells. However, conversion of the bovine alpha CRE homolog to an authentic alpha CRE restored activity to the bovine alpha-subunit promoter in choriocarcinoma cells. Similarly, a human but not a bovine alpha transgene was expressed in placenta in transgenic mice. Thus, placenta-specific expression of the human alpha-subunit gene may be the consequence of the recent evolution of a functional CRE. Expression of the human alpha transgene in mouse placenta further suggests that evolution of placenta-specific trans-acting factors preceded the appearance of this element. Finally, in contrast to their divergent patterns of placental expression, both the human and bovine alpha-subunit transgenes were expressed in mouse pituitary, indicating differences in the composition of the enhancers required for pituitary- and placenta-specific expression.
机译:编码糖蛋白激素α亚基的单拷贝基因在所有哺乳动物的垂体中以及仅灵长类和马的胎盘中表达。我们已经系统地分析了人类和牛α-亚基基因的启动子调节元件,以阐明其组织特异性表达的不同模式背后的分子机制。该分析需要在绒毛膜促性腺激素分泌型人绒毛膜癌细胞系中使用瞬时表达测定,蛋白质-DNA结合测定以及在转基因小鼠中表达人或牛α亚基基因的嵌合形式。从结果,我们得出结论,人类α-亚基基因的胎盘表达需要一个功能性环AMP反应元件(CRE),该元件在启动子调节区以串联重复的形式存在。相反,发现牛α-亚基基因以及大鼠和小鼠基因的启动子调控区含有一个CRE同源物,该同源物与人的CRE同源物只有一个核苷酸。这种差异大大降低了牛CRE同系物对与人αCRE结合的核蛋白的结合亲和力,从而使牛α-亚基启动子在人绒癌组织中失活。但是,将牛αCRE同源物转化为真正的αCRE可恢复绒癌组织中牛α-亚基启动子的活性。类似地,在转基因小鼠的胎盘中表达了人而非牛的α转基因。因此,人α-亚基基因的胎盘特异性表达可能是功能性CRE近期进化的结果。人α转基因在小鼠胎盘中的表达进一步表明胎盘特异性反式作用因子的进化先于该元件的出现。最后,与其胎盘表达的不同模式相反,人和牛的α-亚基转基因均在小鼠垂体中表达,表明垂体和胎盘特异性表达所需的增强子组成不同。

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