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克隆的人二氢睾酮/雄烷二醇UDP-葡萄糖醛酸基转移酶的特性及其与其他类固醇同工型的比较。

Characterization of a cloned human dihydrotestosterone/androstanediol UDP-glucuronosyltransferase and its comparison to other steroid isoforms.

作者信息

Chen F, Ritter J K, Wang M G, McBride O W, Lubet R A, Owens I S

机构信息

Section on Genetic Disorders of Drug Metabolism, National Institute of Child Health and Human Development.

出版信息

Biochemistry. 1993 Oct 12;32(40):10648-57. doi: 10.1021/bi00091a015.

Abstract

A human cDNA, UDPGTh-3, encoding a dihydrotestosterone/5 alpha-androstane-3 alpha,17 beta-diol UDP- glucuronosyltransferase (transferase) has been isolated and characterized. The nucleotide sequence of UDPGTh-3 encodes a 530 amino acid protein with a typical membrane insertion-signal peptide, a membrane-anchoring domain, and three potential asparagine-linked glycosylation sites. Alignment shows that this encoded isozyme is 96% identical to an apparent estriol-metabolizing isoform, HLUG4 [Coffman, B. L., et al., (1990) Arch. Biochem. Biophys. 281, 170-175]. The udpgth-3 isozyme is 78% identical to two other steroid isoforms, HLUG25 (udpgth-1) [Jackson, M. R., et al. (1987) Biochem. J. 242, 581-588; Ritter, J. K., et. al. (1992) Biochemistry 31, 3409-3414] and udpgth-2 [Ritter, J. K., et al. (1990) J. Biol. Chem. 265, 7900-7906]. udpgth-2 and udpgth-1 metabolized parallel substrates (stereospecific estriols, 3,4-catechol estrogens, and the bile salt hyodeoxycholate), except that udpgth-2 was 100-fold more effective than udpgth-1. The mRNA encoding udpgth-3 is 2.4 kb in size and is present in liver, prostate, and testis; the mRNA encoding udpgth-2 is located in liver and kidney, whereas that for udpgth-1 is liver-specific. Each of the liver mRNA species encoding udpgth-3, udpgth-2, or udpgth-1 was induced 2.5-3-fold by phenobarbital treatment of the Erythrocebus patas monkey. In 16 human liver mRNA samples, the message encoding udpgth-3 was generally uniformly expressed and that for udpgth-1 exhibited wide variations in its level, whereas that for udpgth-2 was barely detectable in nine samples and not detectable in the others. Three samples contained no message for either isoform. Substrate turnover by udpgth-3 is ranked as follows: phenolphthalein > 5 alpha-androstane-3 alpha,17 beta-diol > 5 alpha- dihydrotestosterone = 4-hydroxybiphenyl > phenolsulfonphthalein (phenol red) > phenolphthalin. Genes encoding udpgth-3, udpgth-2, and udpgth-1 mapped to human chromosome 4 with genomic DNA from human/mouse and human/hamster somatic cell hybrids; the genes encoding udpgth-1 and udpgth-2 mapped specifically to band 4q28. udpgth-3 exhibited similar Km values both for 5 alpha-dihydrotestosterone (10 microM) and for its metabolite, 5 alpha-androstane-3 alpha,-17 beta-diol (12.5 microM).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

已分离并鉴定出一种编码二氢睾酮/5α-雄甾烷-3α,17β-二醇UDP-葡糖醛酸基转移酶(转移酶)的人cDNA,即UDPGTh-3。UDPGTh-3的核苷酸序列编码一个含有典型膜插入信号肽、膜锚定结构域和三个潜在天冬酰胺连接糖基化位点的530个氨基酸的蛋白质。序列比对显示,该编码的同工酶与一种明显的雌三醇代谢同工型HLUG4 [科夫曼,B. L.等人,(1990) 《生物化学与生物物理学文献》281, 170 - 175] 有96%的同一性。udpgth-3同工酶与另外两种类固醇同工型HLUG25(udpgth-1)[杰克逊,M. R.等人,(1987) 《生物化学杂志》242, 581 - 588;里特,J. K.等人,(1992) 《生物化学》31, 3409 - 3414] 和udpgth-2 [里特,J. K.等人,(1990) 《生物化学杂志》265, 7900 - 7906] 有78%的同一性。udpgth-2和udpgth-1代谢平行底物(立体特异性雌三醇、3,4-儿茶酚雌激素和胆汁盐猪去氧胆酸),只是udpgth-2的效率比udpgth-1高100倍。编码udpgth-3的mRNA大小为2.4 kb,存在于肝脏、前列腺和睾丸中;编码udpgth-2的mRNA位于肝脏和肾脏,而编码udpgth-1的mRNA是肝脏特异性的。用苯巴比妥处理赤猴后,编码udpgth-3、udpgth-2或udpgth-1的每种肝脏mRNA种类均被诱导2.5 - 3倍。在16个人类肝脏mRNA样本中,编码udpgth-3的信息通常均匀表达,编码udpgth-1的信息水平变化很大,而编码udpgth-2的信息在9个样本中几乎检测不到,在其他样本中未检测到。三个样本中两种同工型的信息均未检测到。udpgth-3的底物周转率排序如下:酚酞 > 5α-雄甾烷-3α,17β-二醇 > 5α-二氢睾酮 = 4-羟基联苯 > 酚红 > 酚酞。利用人/小鼠和人/仓鼠体细胞杂种的基因组DNA,将编码udpgth-3、udpgth-2和udpgth-1的基因定位到人类染色体4;编码udpgth-1和udpgth-2的基因特异性定位到4q28带。udpgth-3对5α-二氢睾酮(10 microM)及其代谢物5α-雄甾烷-3α,-17β-二醇(12.5 microM)表现出相似的Km值。(摘要截短于400字)

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