HUMAN ESTROGEN SULFOTRANSFERASE GENE (STE) - CLONING, STRUCTURE, AND CHROMOSOMAL LOCALIZATION

被引:41
作者
HER, C
AKSOY, IA
KIMURA, S
BRANDRIFF, BF
WASMUTH, JJ
WEINSHILBOUM, RM
机构
[1] MAYO CLIN & MAYO FDN,MAYO MED SCH,DEPT PHARMACOL,ROCHESTER,MN 55905
[2] NCI,MOLEC CARCINOGENESIS LAB,BETHESDA,MD 20892
[3] LAWRENCE LIVERMORE NATL LAB,CTR HUMAN GENOME,BIOL & BIOTECHNOL RES PROGRAM,LIVERMORE,CA 94550
[4] UNIV CALIF IRVINE,COLL MED,DEPT BIOL CHEM,NATL HUMAN GENOME RES CTR,IRVINE,CA 92717
关键词
D O I
10.1006/geno.1995.1210
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Sulfation is an important pathway in the metabolism of estrogens. We recently cloned a human liver estrogen sulfotransferase (EST) cDNA. We have now determined the structure and chromosomal localization of the EST gene, STE, as a step toward molecular genetic studies of the regulation of EST in humans. STE spans approximately 20 kb and consists of 8 exons, ranging in length from 95 to 181 bp. The locations of most exon-intron splice junctions within STE are identical to those found in a human phenol ST (PST) gene, STM, and in a rat PST gene, In addition, the locations of five STE introns are also conserved in the human dehydroepiandrosterone (DHEA) ST gene, STD. The 5'-flanking region of STE contains one CCAAT and two TATA sequences. The location of one of the TATA box elements is in excellent agreement with the site of transcription initiation as determined by 5'-rapid amplification of cDNA ends. STE was mapped to human chromosome 4q13.1 by fluorescence in situ hybridization, Cloning and structural characterization of STE will now make it possible to study potential molecular genetic mechanisms involved in the regulation of EST in human tissues. (C) 1995 Academic Press, Inc.
引用
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页码:16 / 23
页数:8
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