STRUCTURAL CHARACTERIZATION OF THE HUMAN ESTROGEN SYNTHETASE (AROMATASE) GENE

被引:139
作者
HARADA, N
YAMADA, K
SAITO, K
KIBE, N
DOHMAE, S
TAKAGI, Y
机构
[1] Division of Molecular Genetics, Institute for Comprehensive Medical Science, School of Medicine, Toyoake, Aichi
关键词
D O I
10.1016/0006-291X(90)91954-Q
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The estrogen synthetase (aromatase, cytochrome P-450AROM) gene has been isolated from human genomic libraries and characterized. The restriction map of 43 positive clones obtained indicated that this enzyme is present as a single copy gene. The aromatase gene is unexpectedly large compared with other forms of the cytochrome P-450 superfamily, spanning at least 70 kilobases. The gene consists of 10 exons and its 5′-untranslated region is divided into 2 exons by an intron of more than 35 kilobases long. This organization of the first exon in the aromatase gene is unique in the cytochrome P-450 superfamily. All the exon-intron junctional sequences conform to the canonical GT AG rule. The sequences of a TATA box and a CAAT box are present 27 and 83 base pairs upstream from the transcriptional initiation site. Within 3 kilobases upstream from the initiation site, there are no typical consensus sequences of responsive elements for glucocorticoid and c-AMP, which regulate aromatase expression. © 1990.
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页码:365 / 372
页数:8
相关论文
共 23 条
[1]   HUMAN AROMATASE - CDNA CLONING, SOUTHERN BLOT ANALYSIS, AND ASSIGNMENT OF THE GENE TO CHROMOSOME-15 [J].
CHEN, SU ;
BESMAN, MJ ;
SPARKES, RS ;
ZOLLMAN, S ;
KLISAK, I ;
MOHANDAS, T ;
HALL, PF ;
SHIVELY, JE .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1988, 7 (01) :27-38
[2]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[3]   AROMATASE-ACTIVITY IN HUMAN GRANULOSA-CELLS DURING FOLLICULAR DEVELOPMENT AND THE MODULATION BY FOLLICLE-STIMULATING-HORMONE AND INSULIN [J].
GARZO, VG ;
DORRINGTON, JH .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1984, 148 (05) :657-662
[6]   UNIDIRECTIONAL DIGESTION WITH EXONUCLEASE-III CREATES TARGETED BREAKPOINTS FOR DNA SEQUENCING [J].
HENIKOFF, S .
GENE, 1984, 28 (03) :351-359
[7]   GENE STRUCTURE AND NUCLEOTIDE-SEQUENCE FOR RAT CYTOCHROME-P-450C [J].
HINES, RN ;
LEVY, JB ;
CONRAD, RD ;
IVERSEN, PL ;
SHEN, ML ;
RENLI, AM ;
BRESNICK, E .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 237 (02) :465-476
[8]  
JOCORBIN C, 1988, P NATL ACAD SCI USA, V85, P8948
[9]  
LEACH DRF, 1983, NATURE, V305, P448, DOI 10.1038/305448a0
[10]  
Maniatis T., 1982, MOL CLONING