首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Role of steroid 11 beta-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans.
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Role of steroid 11 beta-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans.

机译:类固醇11β-羟化酶和类固醇18-羟化酶在人体糖皮质激素和盐皮质激素的生物合成中的作用。

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摘要

A gene encoding steroid 18-hydroxylase (P-450C18) was isolated from a human genomic DNA library. It was identified as CYP11B2, which was previously postulated to be a pseudogene or a less active gene closely related to CYP11B1, the gene encoding steroid 11 beta-hydroxylase (P-45011 beta) [Mornet, E., Dupont, J., Vitek, A. & White, P. C. (1989) J. Biol. Chem. 264, 20961-20967]. The nucleotide sequence of the promoter region of the P-450C18 gene is strikingly different from that of the P-45011 beta gene, although the sequences of their exons are 93% identical. The transient expression in Y-1 adrenal tumor cells of CAT constructs with a series of deletion mutants of promoter regions of both genes indicated that the two genes are regulated differently. P-450C18 as expressed in COS-7 cells exhibits steroid 18-hydroxylase activity to catalyze the synthesis of aldosterone and 18-oxocortisol and exhibits steroid 11 beta-hydroxylase activity as well. In contrast, P-45011 beta as expressed in the cultured cells exhibits steroid 11 beta-hydroxylase activity exclusively but fails to catalyze the synthesis of aldosterone and 18-oxocortisol. These results indicate that P-45011 beta and P-450C18 are products of two different genes and that the former participates in the synthesis of glucocorticoids whereas the latter participates in the synthesis of mineralocorticoids in humans.
机译:从人类基因组DNA文库中分离出编码类固醇18-羟化酶(P-450C18)的基因。它被鉴定为CYP11B2,先前被认为是假基因或活性较低的基因,与CYP11B1紧密相关,该基因编码类固醇11β-羟化酶(P-45011 beta)[Mornet,E.,Dupont,J.,Vitek ,A。&White,PC(1989)J. Biol。Chem。化学264,20961-20967]。 P-450C18基因启动子区域的核苷酸序列与P-45011 beta基因的核苷酸序列显着不同,尽管它们的外显子序列具有93%的一致性。具有两个基因的启动子区域的一系列缺失突变体的CAT构建体在Y-1肾上腺肿瘤细胞中的瞬时表达表明,这两个基因的调控不同。在COS-7细胞中表达的P-450C18表现出类固醇18-羟化酶活性,以催化醛固酮和18-氧代皮质醇的合成,并且还显示出类固醇11β-羟化酶活性。相反,在培养的细胞中表达的P-45011β仅表现出类固醇11β-羟化酶的活性,但不能催化醛固酮和18-氧代皮质醇的合成。这些结果表明,P-45011 beta和P-450C18是两种不同基因的产物,前者参与人糖皮质激素的合成,而后者参与人盐皮质激素的合成。

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